Vitamin D deficiency in Middle East and North Africa - June 2013

Hypovitaminosis D in the Middle East and North Africa: Prevalence, risk factors and impact on outcomes

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Volume 5, Issue 2 April/May/June 2013 Dermato-Endocrinology
http://dx.doi.org/10.4161/derm.25111
Keywords: genetics polymorphisms, infections, musculoskeletal outcomes, osteomalacia, pleotropic, policy, prevalence, region specific guidelines, rickets, risk factors

Authors: Darina Bassil, Maya Rahme, Maha Hoteit and Ghada El-Hajj Fuleihan

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Abstract:
Background: The Middle East and North Africa (MENA) region registers some of the highest rates of hypovitaminosis D worldwide.

Aim: We systematically reviewed the prevalence of hypovitaminosis D, rickets and osteomalacia, their predictors and impact on major outcomes, in the region.

Methods: Medline, Pubmed and Embase search engines, entering keywords and concepts, combined with individual countries of interest, were used. Search was limited years 2000–2012; and review articles were used for the period preceding year 2000.
Results: Rickets and osteomalacia still occur in this sunny region. Hypovitaminosis D prevails, with rates varying 30–90%, considering a desirable serum 25 hydroxy-vitamin D 25(OH)D of 20 ng/ml. Advancing age, female gender, multi-parity, clothing style, season, socio-economic status and urban living are recognized predictors of hypovitaminosis D in adults. Prolonged breastfeeding without vitamin D supplementation and low dietary calcium intake are the recognized risk factors for rickets and hypovitaminosis D in children.. Associations with pain score and disease activity in rheumatologic disorders, viral load and interleukins in hepatitis C, BMI, lipids and insulin sensitivity, blood pressure, heart failure and mortality are described. Sun exposure in adults decreased prevalence of metabolic syndrome in one study. Few randomized vitamin D trials revealed that the majority of mothers or children failed to achieve a desirable 25(OH)D level, even with doses by far exceeding current recommendations. A trial in adolescent girls reveals substantial bone and lean mass increments.

Conclusion: Hypovitaminosis D is prevalent in MENA. The lack of populations based studies, gaps in studies in infants, pre-pubertal children and pregnant women, hinder the development of region specific guidelines and constitute a major obstacle to impact this chronic and most often subclinical disease.
Received: January 15, 2013; Accepted: May 21, 2013; Published Online: April 1, 2013

Provisional Full-Text corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions containing any author galley corrections will be made available soon. When Provisional Full Text is displayed, it will always be open access.

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Introduction

Vitamin D is a steroid hormone that modulates a wide range of molecular and cellular functions, most readily recognized are its beneficial effects on musculoskeletal parameters. Rickets and osteomalacia represent short-term latency manifestation of vitamin D deficiency and osteoporosis the long-term latency manifestation of more subtle chronic deficiencies.¹^,² An increasing body of evidence also supports non-traditional, extra-skeletal, benefits of vitamin D on the immune system, fuel metabolism, cardiovascular system diseases and cancer.²^-⁵ In addition, associations with decreased mortality have been described.⁶

While rickets is almost eradicated in western populations, its prevalence remains unacceptably high in Asia, Africa and the Middle East and resurgence is also registered in ethnic minority groups in some Northern European countries.⁷^,⁸ Conversely, hypovitaminosis D is prevalent worldwide, but is again most notable in Asia and surprisingly the Middle East, despite its plentiful sunshine.¹^,³ Although such observations stem mostly from non-population based studies, they have for the most part been consistent across reviews over the last decade.⁹^-¹⁴ Such findings are explained by the prevalence of specific risk factors for hypovitaminosis D in this region. These include the classic predictors, in addition to conservative concealed clothing style in women in general and in men from gulf countries in particular. The, lack of governmental regulation for food fortification with vitamin D in the region has also been noted

The aim of this paper is to systematically review the prevalence of rickets, osteomalacia and hypovitaminosis D, in the Middle East and North Africa (MENA) region, evaluate relevant predictors and describe the impact of low vitamin D status on relevant outcomes in studies from the region. Implications of the vitamin D guidelines issued by the Institute of Medicine and the Endocrine Society in 2011 will be put in perspective taking into consideration the status of vitamin D in the MENA.¹⁵^,¹⁶

Methods

Definition of Middle East North Africa region
According to the UNICEF, the MENA is composed of 20 countries: Algeria, Bahrain, Lebanon, Egypt, Djibouti, Syria, Occupied Palestinian Territory, Iran, Iraq, Yemen, Tunisia, Sudan, UAE, Saudi Arabia, Jordan, Oman, Libya, Kuwait, Morocco and Qatar.¹⁷ According to the World Bank, countries in the Middle East include United Arab Emirates (UAE), Syria, Qatar, Lebanon, Kuwait, Saudi Arabia, Jordan, Iraq, Iran, Yemen, Oman and Bahrain; and in North Africa Algeria, Egypt, Libya, Morocco, Tunisia and Sudan.¹⁸

Literature search methodology
A systematic review of the literature was implemented targeting the following keywords: vitamin D, vitamin D deficiency or rickets, osteomalacia, conducted separately for each of the individual countries listed above for the Middle East North Africa region (MENA). Each of these keywords were searched on OVID Medline as MeSH terms and also as synonyms or related terms to achieve a comprehensive literature review. The OVID Medline interface was utilized as it allows searching for related MeSH-terms, explode functions, keyword searching in title, abstract and subject headings, adjacency and publication types, in addition to Boolean operators (and, or) and truncation, to identify as many relevant articles as possible. OVID Medline search was conducted from year 1946 until the third week of September, 2012, then tailored to years 2000-Dec 2012 (see Appendix S1). The exact procedure used for every country of the MENA region is detailed in Appendix S1. A PubMed search was also done using the key terms for each of the countries of interest to capture the most recent publications entered into PubMed, not yet indexed in OVID Medline. The following search was entered for each of the countries of the MENA region, the example for Lebanon was: (vitamin D OR rickets OR osteomalacia) AND (Lebanon OR Lebanese). The Embase database was also used to capture a more comprehensive view on studies done in the Middle Eastern region. We also used data compiled in the 2011 International Osteoporosis Foundation (IOF) Middle East Africa Osteoporosis Audit,¹⁹ and additional studies and reviews detailed in the papers retrieved and available in authors' libraries.

Search yield and manuscripts reviewed
A total of 2323 hits were identified from Embase, PubMed and OVID Medline for all the countries, with the exception of Djibouti and Libya, that had no hits. Three screening phases were implemented for identifying relevant articles. The first phase involved screening the titles and abstracts and resulted in 362 manuscripts between 1946 and 2012. The second phase involved deleting studies published before year 2000, thus resulting in 295 papers. The third phase involved retrieving and reviewing the full-text for all 295 papers, of which only 176 where retrievable and these were scored for quality measures based on specific criteria: type of the study (population based yes or no), sample size (n > 100 yes or no), whether the vitamin D assay was specified (yes or no), whether predictors were specified (yes or no) and exclusion criteria were specified (yes/no). Each criterion received a score of 1 if answered positively and articles were sorted into four quality categories: very good for score ≥ 4/5, good for score 3/5, fair for score 2/5 or poor if score 1/5. The large majority of the 295 retrieved papers were from Iran (n = 86), Saudi Arabia (n = 47), UAE (n = 21), Egypt (n = 20), followed by Lebanon, Kuwait, Jordan, Qatar and Morocco Jordan (n = 11−16 each) and Yemen, Tunisia, Iraq, Bahrain, Oman (n = 1−5 each). Out of the total of 176 studies, 109 studies characterized as of very good or good quality are detailed in this review.

For association and intervention studies, as well as reports on rickets or osteomalacia, rating score was not applied and all relevant studies were examined. Titles and abstracts for reviews on osteomalacia retrieved prior to 2000 (n = 338) were screened and all relevant reviews in the MENA, in addition to those on hypovitaminosis D⁹^-¹¹ were used to summarize information for the period preceding year 2000.

Interpretation of results from papers on vitamin D and cut-offs used to determine desirable levels
Serum 25 hydroxy-vitamin D 25(OH)D 25(OH)D level is the best indicator of vitamin D nutritional status. The importance of variations in serum 25(OH)D assays and the lack of their standardization has been recently recognized.²⁰^,²¹ Furthermore, there is no universal agreement on what constitutes a desirable level to optimize musculoskeletal health in elderly Caucasians,¹⁵^,¹⁶ let alone optimal levels across the lifecycle, for other ethnic groups or targeting other major chronic diseases outcomes. Findings from any paper on vitamin D, have to therefore be interpreted in this context. Results for serum 25(OH)D are reported in ng/ml, to convert to from ng/ml to nmol/L multiply the value by 2.5.

Magnitude of the Problem and Predictors of Low Vitamin D Status

Rickets and osteomalacia
Rickets and osteomalacia are conditions that can result from severe vitamin D deficiency, hypophosphatemia or mineralization defects. This paper focuses on those resulting from vitamin D deficiency, best captured by measurement of serum 25 hydroxy-vitamin D 25(OH)D level. Rickets is a childhood condition caused by serious vitamin D deficiency and is characterized by soft and weak bones, slowed growth and skeletal development and convulsions. Rickets, by definition, is a disorder which begins in childhood. If this problem occurs later in life it is known as osteomalacia. In a review on rickets worldwide, covering 30 y from 1968–1998, Prentice et al. noted that Asia, the Middle East and Africa, a region spanning latitudes from 5° to 40° North, registered the highest rates. The reported rates for clinical or radiological rickets were 70% in Mongolia (1998), 66% in Tibet (1994), 44% in Ethiopia (1987), 27% in Yemen (1987), 15% in Iran (1975), 10% in Turkey (1994) and 9% in Nigeria (1998), compared with 1.6% in Manchester minorities mostly Pakistanis.⁷^,⁸ Similarly, a review by our group underscored the lack of adequate population based studies and reported rates to be 10–100 folds higher than those in western populations.¹¹ These include a prevalence of 27% in children < 5 y in North Yemen, 10% in a field sample from rural Egypt, 1% Kuwait if < 2yrs (1981−86), 0.5% of Saudis < 2 y (1997–1999) and 6% in Turkey in 1998 down to < 1% in 2008, the latter following a National Vitamin D supplementation program.¹¹ Rickets accounted for a substantial number of pediatric hospital admissions, 50% of children hospitalized with pneumonia in Yemen, 11% of infant’s admissions with acute illness in Jordan, 6.5% of newborn admissions in Kuwait and 1.8% of pediatric admissions in 1986–88 in Saudi Arabia.⁹^,¹¹ Non-skeletal manifestations of rickets included convulsions in 4−79% of patients, acute chest infections and asthmatic bronchitis in 66% of 500 cases in Saudi Arabia, broncho-pneumonia in 43% of 200 Iranian children and 44% of 250 children from Kuwait. An acute infection or respiratory diseases were the presenting manifestation in 20–60% of cases presenting with rickets in smaller studies from Turkey, Egypt, Jordan and Saudi Arabia, while gastroenteritis accounted for 8–56% of reasons for admission in hospitals in Middle East. Dilated cardiomyopathy was reported in three infants from Asia, one from Turkey and two from UAE.¹¹ Predictors of rickets included, low maternal vitamin D status, prolonged breast feeding, low socioeconomic status (SES), educational level and crowding. It has been recognized that primary vitamin D deficiency does not adequately describe nutritional rickets explained in some African, Middle Eastern and Asian countries and that concomitant low calcium intake and possibly disturbances of phosphate metabolism, renal compromise and iron deficiency may also play an important role in the pathophysiology of the disease.⁹

In our current search, we retrieved 13 publications on rickets, but only 8 were on nutritional rickets. Case series were published in Iran, Saudi Arabia, Kuwait, United Arab Emirates, Qatar and Egypt, with sample sizes ranging 21 to 283 subjects and age ranging from infants all the way to adolescents, with the majority being infants and toddlers.²²^-³⁰ In a study of 98 rachitic children from Egypt and Turkey, mean age 11.7 y, mean 25(OH)D was 14.3 (± 11.2) ng/ml in patients from Egypt and 10.1 (± 7.9) ng/ml in Turkey, compared with mean levels above 20 ng/ml in controls, underscoring a combined etiology that includes insufficient calcium intake, in the pathophysiology of rickets and possibly other factors, especially in Egypt.²⁹ Similarly, in a small study of 16 Emirati children from Abu Dhabi (24°), nutritional rickets from vitamin D deficiency was reported in eight subjects, with a mean 25(OH)D of 7(± 2) ng/ml and a mixed etiology with combined calcium deficiency in the rest with a mean 25(OH)D of 17 (± 8) ng/ml.³¹ Common risk factors included multiparity, prolonged breast feeding, delayed intake of semi-solids, maternal education and complete wrapping of the child.²⁸

Osteomalacia, the adult manifestation of rickets, may be asymptomatic and go undetected, thus making true prevalence studies very difficult. The diagnosis is usually made on basis of the classic clinical profile of bone pain, fractures and proximal myopathy, combined with confirmatory laboratory tests including a low 25(OH)D, usually below 5–10 ng/ml (25–50 nmol/L), low serum calcium and phosphate levels and a high alkaline level . However, the patient may not have hypocalcemia due to correction of serum calcium level from secondary hyperparathyroidism. Moreover, hypovitaminosis D can be misdiagnosed as fibromyalgia, chronic fatigue syndrome or simply depression.³²^,³³ The above 25(OH)D cut-offs are not diagnostic of osteomalacia, as demonstrated in a study in Caucasian subjects.³⁴ We are unaware of such studies in MENA. Convulsions and hypocalcemic cardiomyopathy are also very rare manifestation of severe hypocalcemia from rickets or any other causes.³⁵ To-date, most publications on osteomalacia are limited to case reports or case series, made on basis of a clinical diagnosis.³⁶^,³⁷ The condition can mimic osteoporosis, with severe bone demineralization due to severe vitamin D deficiency, hyperparathyroidism, vertebral compression fractures, T-scores ranging from -5 to -4, with normalization after aggressive vitamin D therapy.

Hypovitaminosis D
Despite limitations caused by the lack of methodological standardization, in general, a serum 25(OH)D at concentration less than25 nmol/L (10 ng/mL) is a useful marker of the risk of clinical deficiency, but the terminology and cut-offs used to define less than desirable vitamin D status is controversial. It includes terms such as insufficiency, inadequate level, sub-optimal level and hypovitaminosis D and may result in subclinical conditions with chronic latent manifestations, the most recognized of which is osteoporosis. The 25(OH)D cut-offs to define this condition vary and have most recently been framed by the 2011 desirable levels of the Institute of Medicine Report set at 20 ng/ml (50 nmol/L),¹⁶ and the Endocrine Society Guidelines set at 30 ng/ml (75 nmol/L).¹⁵ Most studies have however predated these recommendations and used variable cut-offs.

In a review conducted by the nutrition working group of the IOF, hypovitaminosis defined as 25 (OH)D level below 30 ng/ml (75 nmol/L) was prevalent in all regions of the world, whereas levels below 10 ng/ml (25 nmol/L) were most common in South Asia and the Middle East. Predictors of low 25(OH)D levels included older age, female sex, higher latitude, winter season, darker skin pigmentation, less sun exposure, dietary habits and absence of vitamin D fortification.¹² The high prevalence of hypovitaminosis D worldwide, and not only in risk groups, was again underscored in a recent review, Asia and the Middle East being at particular risk, albeit with high variability between studies within the ME.¹³^,¹⁴ The latest attempt at a global representation of vitamin D status in healthy populations, commented on the lack of representative studies, large gaps in information in children, adolescents worldwide and in adults in Central and South America, as well as Africa.¹⁴

One of the original studies on hypovitaminosis D in the Middle East was conducted in apparently healthy 104 male Saudi university students, who had a mean 25(OH)D of 12.8 (± 6.3)ng/ml with 35% < 10 ng/ml³⁸. The high prevalence of hypovitaminosis D in Saudi subjects has been validated in numerous studies. Table 1 summarizes key findings from studies of good or very good quality retrieved from our search, for adults from the MENA region.³⁹^-⁸¹ The overwhelming majority of studies revealed 25(OH)D levels in the low teens 25(OH)D 10−15 ng/ml, even considering population-based studies. Consistent predictors across these studies for lower values were age, albeit with differing findings, some studies showing older age to be a risk factor,⁵⁷^,⁶⁷^,⁶⁹ while others point to younger age,⁴¹^,⁴²^,⁷⁷ female gender in adults⁴¹^,⁶¹^,⁶³^,⁷²^,⁷⁵^,⁸² and children,⁸³^-⁸⁹winter season, sunlight exposure and veiling,⁴⁰^,⁴¹^,⁴⁴^,⁵⁶^,⁶⁰^,⁶³^,⁶⁶^,⁷⁵^,⁷⁸^,⁸¹^,⁹⁰^,⁹²except in some studies from gulf countries where summer registers lowest values in studies from the United Arab Emirates,⁷⁵^,⁷⁷ pollution,⁴³ low calcium or vitamin D dietary intake,⁶⁷^,⁷⁷^,⁸⁰^,⁸¹^,⁹⁰^,⁹² and exclusive breast feeding in infants⁸⁸. Other predictors included high BMI and /or increased adiposity,³⁹^,⁶⁰^,⁶⁶^-⁶⁸^,⁷²^,⁹³ and lower SES status or educational level⁴⁴^,⁶⁰^,⁶⁴^,⁶⁸^,⁸⁰^,⁸³.The impact of menopause was not consistent across studies, whereas premenopausal women had higher levels in the study from Saudi Arabia,⁶⁷ the opposite was found in UAE.⁷⁷Table 1 details studies conducted in adults, Table 2 in children, Table 3 in mothers-neonates, by country, and highlights are underscored here-in.

Table 1. Overview of Studies on 25(OH) D Values in Adults in Middle East and North Africa

Country	Author/Yr	Sampling Method
City (Latitude)	N Gender/ Age	Exclusion criteria specified	Assay type/ Manufacturer	Season Yr	Predictors for low 25(OH)D	25(OH)D Level Mean ng/ml % below cut-off
Middle East
Iran	Baradaran et al. 2012³⁹	Hospital based
Iran (32°N)	259 ♀♂
20–64 y	Yes	EIA/IDS	NA 2010	High adiposity,
high BMI	12 ± 6
Median: 10
	Kashi et al. 2011⁴⁰	Telephone population based Sari (37°N)	232 ♀,118♂
11–69 y	Yes	ELISA/DRG	End of summer
and winter NA	High humidity climate, winter	Summer: 13.4 ± 13
Winter: 11.7 ± 11
	Hovsepian et al. 2011⁴¹	Outpatient clinic
Isfahan (32°N)	243 ♂, 868 ♀
20–80 y	Yes	RIA/ Biosource	Autumn/ Winter-Spring/ Summer NA	Young age, women	Median Spring: 21 (2–300)
Median Summer: 18 (3–208)
Median Autumn: 19 (1.5–425)
Median Winter: 17 (2–281)
27% < 10, 24% 10–20, 20% 20–30
	Kaykhaei et al. 2010⁴²	Population based
Zahedan (30°N)	431 ♂, 562♀
20–88 y	No	CIA/ DiaSorin	June -Aug 2008	Younger age	13.8
95% < 30 85% < 20
10% 20–30 5% 30–150
	Hosseinpanah et al. 2010⁴³	Clustered sampling Tehran (35° N),
Ghazvin (36°N)	200♀
20- 55 y	Yes	EIA/DRG	Sept 2007	Air pollution	Ghazvinian: ♀ 18 ± 11
Tehranian: ♀ 13 ± 7
Tehranian: 36% < 10 54% 10–20
Ghazvinian: 31% < 10 32% 10–20
	Maddah et al. 2009⁴⁴	Clustered sampling
Guilan (37°N)	427 ♀ Urban
219 ♀ Rural
51–92 y	No	Commercial kit/ BioSource	Oct 2004-Feb 2005	Low education, urban living	♀ Urban: 18.5 ± 13.5
♀ Rural: 22.9 ± 13.8
	Masoompour et al. 2008⁴⁵	Clustered sampling
Shiraz (30°N)	520 ♂
20–74 y	Yes	IRMA/IDS	Jan-Mar 2001	NA	14 ± 6.8
34% ≤ 10
	Hosseinpanah et al. 2008⁴⁶	Population based study Tehran (35°N)	245 p.m.♀
40–80 y	Yes	RIA/IDS	NA	NA	5% < 10 38% 10–20
43% < 20 25% > 32
	Hashemipour et al. 2006⁴⁷	Clustered sampling
Tehran (35°N)	1210 ♂♀
20–69 y	Yes	RIA/IDS	NA	NA	12.9 ± 16.5
9% ≤ 5 56% 5–10
	Rassouli et al. 2001⁴⁸	Densitometry center Tehran (35°N)	73 p.m.♀
49–63 y	Yes	HPLC	Feb-June 2000	NA	Winter: 13.3 ± 5.0
Spring: 18.3 ± 12
36% < 12
Occupied Palestine/Israel	Saliba et al. 2012⁴⁹	Population Based CHF covers > 50% of Israeli population (31°N)	198,834♀♂
Median 60 y	Yes	CIA/ Diasorin	Jan-Dec 2009	Female gender, winter, adults, Arabs > Jews	Summer-Autumn: 22.52 ± 9.8
Winter-Spring: 18.72 ± 9.4
14% < 10 31% < 15
50% < 20 16% > 30
	Saliba et al. 2012⁵⁰	Population Based	2571♂, 6310♀
56.1 ± 17.6 y (1st test)
57.6 ± 17.7 y (Last test)	Yes	CIA / Diasorin	Jan 2008-Sep 2011	Female gender	First test: 20.68 ± 9.6 50% < 20
Last test: 22.68 ± 9.88 41% < 20
*First and last test done in the same month
Middle East
	Saliba et al. 2012⁵¹	Population Based	182, 152 ♀♂
VitD ≤ 13: 59.4 ± 17.4yrs
VitD13–20: 61 ± 16.1 y
VitD20–26: 61.1 ± 16 y
VitD > 26: 59.9 ± 17.1yrs	No	CIA/ Diasorin	Jan 2008 - Dec 2009	History of diabetes
History of Cardiovascular disease	25% ≤ 13ng/ml, mean 9.3 ± 2.7
25% 13–20 ng/ml, mean 16.8 ± 1.8
25% 20–26ng/ml, mean 22.8 ± 1.8
25% > 26ng/ml, mean 32.6 ± 6.4

	Tsur et al.
2011⁵²	Institution based Jerusalem (31.7°N)	74♂ students
(A) Ultra-orthodox Indoors 20.1 ± 0.6yrs
(B) Ultra-Orthodox Outdoors 33.0 ± 4.2yrs
(C) Religious 19 ± 2.0yrs	Yes	RIA /DLS	Mar-Apr NA	Low sun exposure, traditional clothing	(A) 8.9 ± 3.6 100% < 20 65% < 10
(B) 10.2 ± 5.7 91% < 20 65% < 10
(C) 21.7 ± 10.4 51% < 20 12% < 10
	Saliba et al. 2011 ⁵³	Population Based
(31°N)	19,172 ♂♀
63.7 ± 15.5 y
Normal:19,172
Renal failure:5449	No	CIA/ Diasorin	Jan-Dec 2009	Renal Failure	Renal Failure: 22.8 ± 11
Normal Function: 25.32 ± 10.64
	Steinvil et al. 2011⁵⁴	Retrospective
Population based (31°N)	26,699♀ 55 ± 15 y
8175♂ 55 ± 17 y	No	RIA /Diasorin	Jan-Dec 2001–2008	Low sun exposure	♂ 23.22 ± 10.1 79% < 30
♀ 22.7 ± 9.9 78% < 30
	Oren et al.
2010⁵⁵	NA
(31°N)	100♀, 95♂
50yrs	No	CIA/ Diasorin	Feb-Jan NA	Older Age, Ashkenazi > Sephardic > Arab	22.9 ± 10.1
78% < 30
Jordan	Nichols et al. 2012⁵⁶	National micronutrient survey
Jordan (31°N)	2032 ♂ 15–49 y	No	LC-MS/MS	Mar-Apr 2010	Urban living, veiling	Median: 11 96% < 20 60% < 12
No cover n = 98 40% < 12
Scarf/hijab n = 1842 62% < 12
Niqab (full) n = 73 68% < 12
	Batieha et al. 2011⁵⁷	National population based
Jordan (31°N)	1128 ♂, 3462 ♀
> 18 y	No	RIA/ Biosource	July–Oct-Nov 2009	Older age, middle and south region, winter season, low altitude, sunscreen use, indoor work, urban, veiling	♂ 73.3 ± 29.3
94% ≥ 30 4% 20–29.9 2% < 20
♀ 39.8 ± 20.7
63% ≥ 30 23% 20–29.9 14% < 20
	Mallah et al. 2011⁵⁸	NA
Jordan (31°N)	201 ♀, 99 ♂
29–32 y	No	ELISA/IDS	November 2010	Veiling	♂18 ± 4 ♀ 12 ± 5
Western Style: 16 ± 3
Hijab: 12.5 ± 2.5
Niqab: 11.4 ± 1.52
	Mishal 2001⁵⁹	Hospital based
Jordan (31°N)	131 ♀, 23 ♂
18- 45 y	Yes	RIA/Diasorin	Summer: July–Sep Winter: Jan–Mar NA	Winter, veiling	3% < 5 60% 5–12
Both seasons: 62% < 12
Summer: 50% < 12
Winter: 73% < 12
Middle East
Lebanon	Gannaje-Yared et al. 2009⁶⁰	Hospital based
Lebanon (33°N)	151 Christians,
100 Muslims ♀
50–87 y	Yes	CIA/Nichols	July –Aug 2004
Feb-Mar 2005	Dress code covering the arms, high BMI,
low education	19·5 ± 9·8
	Arabi et al. 2006⁶¹-2010⁶²	Population based
Beirut (34°N)	286♀,157 ♂
65–85 y
Mean 73 y	Yes	RIA/ IDS	Nov 2002-Mar2003	Female gender	11.4 ± 4.9
♀ 55% < 10
♂ 37% < 10
	Gannaje-Yared et al. 2000⁶³	Community centers
Bekaa, Beirut (34°N)	99 ♂, 217 Prem♀
30–50 y	Yes	RIA/ Incstar		Veiling,
♀ rural living, ♂urban living,
low vit D intake	9.7 ± 7.1
31% (42% ♀, 7% ♂) < 5
73% (84%♀, 49% ♂) < 12
80% (89% ♀, 51% ♂) < 15
Saudi Arabia	Ardawi et al. 2012⁶⁴	Population based
Health Care Centers
Jeddah (22°N)	834 ♂ 20–74yrs
42.1 ± 13.9 y	Yes	CIA/ Liaison	Jun 2008-Jun 2009	Heavy weight, summer, smoking, no education, sedentary lifestyle, low Vit D supplementation, low sun exposure	Total: 11.6 ± 6.45
< 50 y: 12.5 ± 7.01
≥ 50yrs: 10.7 ± 5.992
88% < 20 10% ≥ 20–30
	El Shafie et al. 2012⁶⁵	Healthcare Center
Riyadh (25°N)	50 married couples
♂40.1 ± 7.4 y
♀30.6 ± 6.8yrs	Yes	ECLIA/Roche	Dec 2010 - Jan 2011	Male gender, high physical activity, milk intake	♀ 8.5 ± 3.9 70% < 10 98% < 20
♂ 12.2 ± 5.5 40% < 10 92% < 20
	Kanan et al. 2012⁶⁶	Retrospective
out-patient clinics
Riyadh (25°N)	1556 ♀
Summer
44.4 ± 16.1 y
Winter
46.1 ± 15.9 y	Yes	HPLC	Jan- Dec 2009	Low latitude, veiling,
sun avoidance	13.3 ± 0.7 Prem Summer 80% < 20
11.4 ± 0.5 Prem Winter 85% < 20
17.7 ± 0.9 p.m. Summer 68% < 20
14.5 ± 0.6 p.m. Winter 76% < 20
	Ardawi et al.
2011⁶⁷	Population based
Health Care centers
Jeddah (22°N)	1,172 healthy ♀
50.9 ± 12.6 y	Yes	CIA/ Liaison	Jun 2008-Jun 2009	Older age, high BMI, low sun exposure, poor dietary,
low vit D supplementation, high WHR	17.18 ± 12.19 (Prem)
13.32 ± 9.94 (PM)
11% (6% Prem 14% PM) < 5
46% (38% Prem 51% PM) < 10
34% (34% Prem 34% PM) 10–20
9% (11% Prem 7% PM) 20–30
12% (16% Prem 8% PM) ≥ 30
	Alissa et al.
2011⁶⁸	Hospital based
Jeddah (22°N)	122 p.m.♀
46–70 y	Yes	RIA/ Diasorin	NA	High SES,
heavy weight, low activity	9.6 ± 0.47 (Controls) 100% < 20
12.7 ± 1.06 (Osteopenic) 97% < 20
Middle East
	Sadat-Ali et al.
2011⁶⁹	Hospital based
Al-Khobar (26°N)	400 Peak Bone Mass age group and ≥ 50yrs	Yes	RIA / Wallac	Feb -May 2008	Older age	PBM age group
11% ♀ 10% ♂ < 20
19% ♀ 19% ♂ 20–30
70% ♀ 71% ♂ > 30
≥ 50 y
19% ♀ 12% ♂ < 20
36% ♀ 25% ♂ 20–30
45% ♀ 63% ♂ > 30
	El Sammak et al. 2011⁷⁰	Hospital based
Al-Khobar (26°N)	87 ♂, 52 ♀ blood donors	Yes	CIA/ Liaison	Dec 2008- Mar2009	Veiling	♂ 10.1 ± 4.5
♀ 9.9 ± 4.5
	El Sammak et al. 2010⁷¹	Hospital based
Al-Khobar (26°N)	87 ♂ 30.0 ± 8.5yrs
52 ♀ 31.0 ± 7.2yrs	Yes	CIA/Liaison	Dec 2008-Mar 2009	NA	♂ 10.1 ± 4.7
♀ 9.9 ± 4.5
	Al-Elq et al.
2009⁷²	Hospital based
Al-Khobar (26°N)	200 ♂ 46.5 ± 14.6yrs 200 ♀ 42.6 ± 15.9yrs	Yes	RIA/Wallac	Feb-May 2008	Older age, life Style, higher BMI ♂, lower BMI♀	♂ 31.1 ± 10.7
♀ 28.9 ± 10.7
	Sadat-Ali et al.
2009⁷³	Hospital based
Al-Khobar (26°N)	100 ♂ 28.2 ± 4.5yrs
100 ♂ 59.4 ± 15.6yrs	Yes	RIA/ Wallac	Feb-May 2008	Low sun exposure	Younger:
Mean 16.6 ± 3.4 in those ≤ 20
Mean 25.4 ± 2.7 in those > 20- < 30
Older:
Mean 16.7 ± 3.4 in those ≤ 20
Mean 25.3 ± 3.3 in those > 20–30
	Al-Turki et al.
2008⁷⁴	Hospital based
Al-Khobar (26°N)	200 ♀
25–35 y (Group 1)
≥ 50 y (Group 2)	Yes	RIA/ Wallac	Feb -May 2008	Low sun exposure, low vit D diet	Group 1:
11% < 20 19% 21–29 70% > 30
Group 2:
19% < 20 36% 21–29 45% > 30
UAE	Al Anouti et al.
2011⁷⁵	University based
Al-Ain (24° N)	208 ♀ 20.8 ± 4.0 y
70 ♂ 21.0 ± 4.6 y	No	HPLC	Oct 2009 138♀70 ♂
Apr 2010 70 ♀	Low sun exposure, female gender	Summer ♀ 8.3 ± 5.9
♂10.9 ± 6.2
Winter ♀ 12.5 ± 4.9
	Dawodu et al.
2011⁷⁶	Pilot Study
Al-Ain (24° N)	8 Healthy Arab ♀
20–30 y.	Yes	HPLC	Sep –Nov 2001	Decreased surface area of the skin exposed,
sun exposure
low vit D intake	Expose face, arms and hands 15 min/ d twice a week for 4 weeks
pre-intervention 7.04
post intervention 9.2
	Saadi et al.
2006⁷⁷	Local clubs,
primary care clinics, local hospitals
Al-Ain (24° N)	175Prem 84PM♀
Prem: 37.5 ± 9.5 y
PM: 58.3 ± 8.9 y	Yes	RIA/Diasorin	Jan 2003-Jun 2005	Younger age,
low vit D intake, summer	10.1 ± 4.3 Prem: 9.7 ± 4.2
PM: 10.9 ± 4.5
All ♀ vit D < 32
Apr 11.6 ± 5.2
Aug 7.2 ± 2.3
North Africa
Morocco
	El Maghraoui et al. 2012⁷⁸	Hospital based
Rabat (34°N)	178 p.m. ♀
≥ 50 y	Yes	ECLIA/Roche	Summer 2010	NA	15.8 ± 11.6
85% < 30
66% < 20
52% < 10
	Allali et al. 2009⁷⁹	Hospital based Rabat (34°N)	415 ♀
24–77 y	Yes	CIA/Diasorin	Summer NA	Older age, lack of sun exposure, veiling, Ca intake < 700 mg	91% < 30
43% < 15
4% < 5
Tunisia	Bahlous et al. 2009⁸⁰	NA
Manouba (37°N)	134 p.m. ♀ with osteoporosis	Yes	HPLC	March–April 2004	Osteoporosis	Fracture pts: 27.5 ± 15.1 51% < 20
Non fracture pts: 21.3 ± 13 25% < 20
	Meddeb et al.
2005⁸¹	NA
Ariana (37°N)	261♀ 128♂
20–60 y	Yes	RIA/Incstar	Jan-March 2002	Older age, veiling, high parity, postmenopausal	47% < 15, 16% 5–10
36% 20–28 y
60% 50–59 y

Abbreviations in table listed here in alphabetical order: BMI: Body Mass Index; Ca: Calcium; CIA: Chemiluminescent Assay; EIA: Enzyme immunoassay; ELISA: Enzyme-linked immunosorbent Assay; ECLIA: Electrochemiluminescent Immunoassay; HPLC: High-performance liquid chromatography; IDS: Immunodiagnostic Systems; IRMA: Immunoradiometric Assay; LC-MS: Liquid Chromatography–Mass Spectrometry; NA: Not Available; PM: Post-Menopausal; Prem: Pre-Menopausal; PBM: Peak Bone Mass; RIA: Radioimmunoassay; SES: Socio-Economic Status; Vit: Vitamin ; WHR: Waist Hip Ratio ; Yrs: Years

Table 2. Overview of studies on 25(OH) D values in Children in Middle East

Country	Author/Yr	Sampling Method City (Latitude)	N Gender/ Age	Exclusion criteria specified	Assay type/ Manufacturer	Season Yr	Predictors for low 25(OH)D	25(OH)D Level Mean ng/ml % below cut-off
Iran	Ghergherechi et al. 2012⁹³	Children hospital Tabriz (38°N)	52 Obese children
4–16 y
57 Control	Yes	CIA/ Nichols	NA 2009–2011	Obesity, high BMI	Case: 32.7 ± 29.6
Control: 44.2 ± 11.2
	Neysestani et al. 2012⁸⁶	Random systematic
districts schools
Tehran (35°N)	573 Boys, 538 Girls
9–12 y	Yes	Competitive protein-binding assay/ IDS	Fall-winter
2007–2008	Female gender	Boys: 11
Girls: 8
	Olang et al. 2011⁸⁷	Vaccination heath centers
Tehran (35°N)	7112 infants
15– 23 mo	Yes	HPLC	May– June2001	Female gender	24.5
3% < 10 33% < 20
44% 20–30 20% > 30
	Ardestani et al. 2010⁹¹	School random sampling
Isfahan (32°N)	271 Boys, 242 Girls 6–7 y	Yes	RIA/ Incstar	Summer 2006	Low intake of vitamin D, low sun exposure, dress style	46 ± 17
3% < 20
	Razzaghy Azar 2010⁸⁹	Clinic university hospital
Tehran (35°N)	192 Girls, 121 Boys 8–18 y	Yes	EIA/ IDS	Apr 2006-Apr 2007	High BMI, puberty stage, female gender	25% (Boys 8% Girls 92%) < 5
27% (Boys 34% Girls 66%) 5–10
26% (Boys 58% Girls 42%) 10–20
	Dahifar et al. 2007³⁰	One middle school
Tehran (35°N)	414 Girls
11–15 y	Yes	Gamma counter/ Genesys	Dec 2002- Mar 2003	NA	30 ± 15.8
	Moussavi et al. 2005⁸⁴	High school Sampling
Isfahan (32°N)	153 Boys, 165 Girls 14–18 y	Yes	RIA/ Biosource	NA 2004	Female gender	Total: 46.2% < 20
Boys: 37.3 ± 18.8
18% < 20 1% < 8
Girls: 16.8 ± 8.4
72% < 20 14% < 8
Jordan	Abdul Razzak et al. 2011⁸⁸	Hospital based
Amman (32°N)	136 Infants,
139 Toddlers
6–36 mo	Yes	EIA/ IDS	Oct 2008- Jan 2009	Sun exposure < 30 min, female gender, exclusive breast feeding	17% < 15
11% < 20
28% < 30
44% > 30
	Jazar et al.
2011⁹⁷	Pediatrics Clinic Jordan (31°N)	100 Boys 1–3 y
100 Girls 3–6 y	Yes	ECLIA/ Roche	May – June 2009	Older age, high BMI, low outdoor activity indoor physical activity, nutrition	Toddler: 26.2 ± 1.2
Preschool children: 21.5 ± 1.2
17% ≤ 15
16% 15- 20
	Gharaibeh et al. 2009⁹⁸	Local community center
Jordan (31°N)	93 Mothers 30yrs Children 60.7 mo	Yes	ELISA/IDS	June -July 2007	Low milk intake,
high income > 212$/month	Mother: 10.2
2% < 5 49% < 10 98% < 20
Children: 22.3 82% < 20 15% > 30
Lebanon	El Hajj-Fuleihan et al. 2007⁹⁹	School based
Beirut (33.5°N)	180 Boys13.1 ± 2 y	Yes	RIA/ Diasorin	Winter- Spring 2001–2002	NA	17 ± 7
	El Hajj-Fuleihan et al. 2006¹⁰⁰	School based
Beirut (33.5°N)	179 Girls 13.1 ± 2 y	Yes	RIA/ Diasorin	Winter- Spring 2001–2002	NA	14 ± 8
	El Hajj-Fuleihan et al. 2001⁸³	School based
Beirut (33.5°N)	Spring:
81 Boys, 88 Girls 13.3 ± 1.6yrs
Fall:
83 Boys, 94 Girls
13.3 ± 1.7yrs	Yes	RIA/ Diasorin	Spring- Fall 1999	Spring season, female gender, age, Tanner staging, low sun exposure,
calcium intake, vitamin D intake, BMI	Spring:
Total:17 ± 8 21% < 10 44% 10–20
Boys:19 ± 7 9% < 10 46% 10–20
Girls:15 ± 8 32% < 10 42% 10–20
Fall:
Total: 22 ± 7 4% < 10 36% 10–20
Boys: 24 ± 6.2 25% 10–20
Girls: 19 ± 7 7% < 10 46% 10–20
Qatar	Bener et al.
2009¹⁰³	Primary Health Care Centers
Doha (25.3°N)	458
Mean 10.9 ± 3.54 y in those < 20 ng/ml
Mean 9.54 ± 3.98 y in those 20–80 ng/ml	No	RIA/ Diasorin	Aug 2007-Mar 2008.	Older Age, non White low sunlight expos, low physical activity, low dietary vit D, family history of vit D deficiency	69% < 20 ng/ml, mean 13.4 ± 8.9
31% < 20 ng/ml, mean 27.5 ± 8.3
Saudi Arabia	Al-Ghamdi et al. 2012⁸⁵	School-based
Jeddah (22°N)	150 ♂ 7–16 y
150 ♀ 6–18 y	Yes	ECLIA/ Roche	May NA	Female gender	16.5 ± 3.7 (6–9 y ♀)
24.5 ± 5.2 (6–9 y ♂)
22 ± 4.5 (10–12 y ♂)
12.6 ± 3.7 (10–12 y ♀)
19.6 ± 5.2 (13–14 y ♂)
11.6 ± 3.6 (13–14 y ♀)
8.8 ± 3.8 (15–18 y ♀)
15.7 ± 5.6 (15–18 y ♂)
	Al Othman et al. 2012⁸²	Primary Health Care Centers
Riyadh (25°N)	331 (153♂178 ♀)
Physically inactive:
13.4 ± 3.2 y
Moderate Activity:
12.6 ± 3.3 y
Active: 12.1 ± 3.6 y	Yes	ELISA /IDS	Mar- Dec 2010	Low physical activity, low sun exposure	7.1 ± 0.6 (Physically In Active)
8.5 ± 0.6 (Moderate Activity)
9.1 ± 0.6 (Active)
11% < 5 72% 5–10 17% 10–20
	Kensarah et al. 2012¹⁰²	School-based
Makkah (21°N)	87 ♂ 61♀
♂10.4yrs,♀9.6yrs	Yes	ECLIA /Roche	NA	Female gender	97% ♀ < 20
78% ♂ < 20
UAE	Rajah et al.
2012¹⁰¹	Pediatric outpatient clinics
Abu Dhabi(24°N)	183 (52% ♂)
5.32 ± 3.76 y	Yes	RIA /Diasorin	All year 2005–2008	Sedentary lifestyle, veiling, Ca deficient diet.	Total:21.4 18% > 10
27.5 (0–0.9yrs) 31 (1–2yrs)
21.2 (2–8yrs) 14.1(8–12yrs)
	Dawodu et al. 2003⁹⁰	Maternal and child health clinics
Al-Ain (24° N)	90 unsupp breast feeding Infants and Mothers	Yes	HPLC	Apr- Oct 1999	Low dietary vit D intake, low sun exposure	Mothers 8.6 (61% < 10)
Infants 4.6 (82% < 10)
	Dawodu et al. 2001¹⁰⁴	Hospital based
Al-Ain (24° N)	51
15.4 mo
UAE nationals (26) non-Gulf Arabs(25)	Yes	HPLC	Feb- Sep NA	Low Vit D supplementation	Infants 22% < 10
25 ± 11.9 (dietary Vit D supp)
15.4 ± 10.9 (unsupp)
Mothers 50% < 10
11.36 ± 5.6

Abbreviations in table listed here in alphabetical order. BMI: Body Mass Index; CIA: Chemiluminescent Assay; EIA: Enzyme immunoassay; ELISA: Enzyme-linked immunosorbent Assay; ECLIA: Electrochemiluminescent Immunoassay; HPLC: High-performance liquid chromatography; IDS: Immunodiagnostic Systems; NA: Not Available; RIA: Radioimmunoassay; Supp: Supplemented; Unsupp: Unsupplemented; Vit: Vitamin; Yrs: Years

Table 3. Overview of Studies on 25(OH) D Values in Pregnant Women/Neonates in Middle East

Country	Authors/Yr	Sampling Method City (Latitude)	N/ Age	Exclusion criteria specified	Assay type/ Manufacturer	Season /Yr	Predictors for low 25(OH)D	25(OH)D Level Mean ng/ml % below cut-off
Iran	Asemi et al. 2010¹⁰⁹	Maternity clinic Kashan (34°N)	147 pregnant ♀
18–35 y	Yes	HPLC	NA/ 2008–2009	NA	15 ± 8
	Kazemi et al. 2009¹⁰⁸	Maternity clinics general hospital Zanjan (37°N)	67 full-term pregnant mothers 28.5 ± 5 y and 61 neonates	Yes	ELISA	Mar- Sep 2005	Winter for maternal and cord blood	Mother 8 ± 1.5 Summer 13 Winter 3
Cord 7 ± 1 Summer 8.7 Winter 5
	Bassir et al. 2001¹¹⁰	Maternity Hospital Shohalda
Tehran (25–35°N)	50 mothers 16–40 y and their neonates	Yes	Radioligand assay	Jan- Sep 1997	NA	Mother 5 ± 2 80% < 10
Cord 2
Israel	Mukamel et al. 2001¹¹¹		156 Orthodox and 185 non- Orthodox Jewish mothers
at delivery	Yes	Competitive Protein Binding Assay	All year 1998–1999	Sect	Orthodox 13.5 ± 7.5
5% < 5 32% < 10
Non-Orthodox 18.6 ± 9.6
3% < 5 13% < 10
Kuwait	Molla et al. 2005¹¹²	Hospital based n = 2
Kuwait city (29 °N)	214 pregnant mothers 27.7yrs
and their neonates	Yes	RIA/ Incstar	All year 1999–2000	NA	Mothers 13–17
Neonates 8
40% mothers, 60% neonates < 15
UAE	Narchi et al. 2010⁹²	Maternal and Child Health
Al Ain (24°N)	75 pregnant from early pregnancy to 6 mo postpartum
18–40 y	Yes	RIA/IDS	Sep-Nov 2007	Dietary habits,
voluntary avoidance of sun exposure, veiling	First antenatal visit 17.3 ± 10.5
After delivery 14.4 ± 9.8
At 6 mo 11.9 ± 11.2

Abbreviations listed in alphabetical order: ELISA: Enzyme-linked immunosorbent Assay; HPLC: High-performance liquid chromatography; IDS: Immunodiagnostic Systems; NA: Not Available; RIA: Radioimmunoassay; Yrs: Years

Adults in Middle EastIran
The mean 25(OH)D level in several cross-sectional studies of good to very good quality was in the low teens 25(OH)D 10−15 ng/ml,³⁹^,⁴⁰^,⁴²^-⁴⁵ and the majority of these studies used randomized cluster sampling that was population based, be it at city level or nation level.

Jordan
Quite opposing results were found in two large, recent, population based studies graded as very good. The first included 4590 subjects and revealed a surprising high mean 25(OH)D level of 73 ng/ml in males and 40 ng/ml in females,⁵⁷ levels that remain unmatched in any other study or population. Conversely, a study of 2032 women, age 15−49 y revealed a median vitamin D of 11 ng/ml, 96% of subjects had levels below 20 ng/ml, and 60% were below a cut-off of 12 ng/ml.⁵⁶ While the former study used a Biosource assay, the latter used the gold standard LCMS assay to measure vitamin D. Aside from assay differences, reasons for such wide discrepancies remain unexplained.

Lebanon
Several studies including a population-based study conducted in elderly subjects revealed mean 25(OH)D levels varying between the low-high teens 25(OH)D 12–18 ng/ml.⁶⁰^,⁶¹^,⁹⁴In an interesting sub-set analysis of a large international study in post-menopausal women, Lebanese Muslim women had lower levels than Christian women, findings that could in part be explained by dress style and higher BMI in Muslims.⁶⁰

Occupied Palestine/Israel
In general 25(OH)D mean levels were higher than those recorded in other countries in Middle East, including those reported in several large scale studies that took advantage of Health Maintenance Organization (HMO) or Non-Governmental Organization (NGO) databases, averaging around 20 ng/ml.⁵¹^,⁵³^,⁵⁴ One ecological study revealed vitamin D levels to be highest in Ashkenazi Jews and lowest in Arabs.⁵⁵

Saudi Arabia
While several large sample population based studies as well as smaller studies revealed a high prevalence of hypovitaminosis D in Saudi Arabia (> 80% below 20 ng/ml),⁶⁴^,⁶⁶^,⁷⁰ few smaller studies revealed replete levels.⁷²^,⁷⁴ In a sample of 1,172 women from of population-based survey of 40 primary health care centers around the city of Jeddah, 80% of subjects had a 25(OH)D level below 20 ng/ml. Mean levels in pre-menopausal women were 17 and in post menopausal women were 13 ng/ml.⁶⁷ Similarly a mean level of 12 ng/ml was found in a sample of 834 adults men, age 42 y.⁶⁴

United Arab Emirates
The mean levels from the three studies listed in Table 1 are close to 10 ng/ml, with inverse seasonal pattern.⁷⁵^-⁷⁷

Adults in North Africa
Studies from this region are scarce, limited to Morocco and Tunisia. Two hospital-based studies conducted in women in Rabat revealed a 25(OH)D level in the mid-high teens.⁷⁸^,⁷⁹ Studies in Moroccan immigrants revealed similarly low levels.⁹⁵^,⁹⁶ A study of 100 immigrants with mean age of 49 y, showed a mean 25(OH)D of 11 ng/ml and 90% of subjects had mean levels below 20 ng/ml.⁹⁶Findings were not different in Tunisian women, with mean levels again noted in mid-teens.⁸⁰^,⁸¹

Children and adolescents in the Middle East
As detailed in Table 2³⁰^,⁸²^-⁹¹^,⁹³^,⁹⁷^-¹⁰⁴ most studies reported mean 25(OH)D levels in teens or close to 20 ng/ml, thus again revealing a large proportion of apparently healthy children, that is 30–75%, to have 25(OH)D levels below this deemed desirable cut-off.

Iran
Registered the largest number of studies with wide variations in 25(OH)D levels, in general being lower in winter, in girls and in older children. The proportion of subjects with 25(OH)D level below 20 ng/ml was 33% in 7,112 infants and toddlers in Tehran (36° North) in early summer,⁸⁷ 3% in a sample of 513 young school children, age 6−7 y in Isfahan (33° North) in the summer,⁹¹ up to 78% in school adolescents from Tehran in the spring,⁸⁹ and 46% in high school students.⁸⁴ Mean levels were quite low in the winter in 1,111 older school children from Tehran, measured at 11ng/ml in boys and 8 ng/ml in girls,⁸⁶ and surprisingly high in middle school girls in Isfahan in winter.³⁰

Jordan
Two studies conducted in hospital based clinics in Amman, in toddlers and pre-school children, one in summer and the other in the winter, revealed that one-third of subjects had mean 25(OH)D levels below 20 ng/ml,⁸⁸^,⁹⁷ while a community based sample in 93 children mean age 60 mo, in the summer of 2007, revealed the proportion to be even higher at 82%.⁹⁸

Lebanon
Two separate studies reported mean 25(OH)D levels in mid-teens conducted in school adolescents from greater Beirut.⁸³^,⁹⁹^,¹⁰⁰ Between 30–40% had a mean 25(OH)D levels below 20 ng/ml, proportions being higher in the winter and in girls.

Saudi Arabia
A school-based study reveals 25(OH)D levels in mid-high teens in children, being lower in girls than boys, whereas mean levels were below 10 ng/ml in a study of adolescents recruited from primary health care centers in Ryadh.⁸²^,⁸⁵

United Arab Emirates
In study of 183 children, age 1−12 y, selected from an urban ambulatory clinic in Abu Dhabi, there was a decrease in 25(OH)D levels with age from infancy to early adolescence; 21% of girls and 16% of boys had a 25(OH)D below 10 ng/ml, and the proportions were 46% and 32% respectively for a cut-off below 20 ng/ml.¹⁰¹ Levels were lower in mother and infants from 2 hospital based studies, where 61% of the mothers and 82% of the 78 infants tested had hypovitaminosis D (serum 25(OH)D < 10 ng/ml).⁹⁰^,¹⁰⁴

Qatar
In a small study of 65 school girls, age 9−15 y, 25(OH)D levels were below 20 ng/ml in 98%.¹⁰⁵ The weighted average for 25(OH)D was 17.5 ng/ml level in 458 subjects, age < 16 y, attending a primary health clinic and was less than 20 ng/ml in 69%.¹⁰³

We could not identify any studies conducted in children and adolescents for countries in North Africa.

Pregnant women and neonates
A systematic review of first trimester normative 25(OH)D levels, of 18 studies across the world, revealed mean 25(OH)D levels ranging between 29 and 73 nmol/L in white Caucasian women and between 15–26 nmol/L in Turkish and Moroccan and other non-western women in Netherlands.¹⁰⁶ Similarly, a high prevalence of low 25(OH)D levels was reported in ethnic minority groups in western countries, the prevalence ranged between 59–84% in the Netherlands, exceeded 50% in the UK, averaged 61% in New Zealand, was above 80% in Australia, using a cut-off of 10 ng/ml; and it was 5–30% in the US at a cut-off of 15 ng/ml.⁷ Investigations in Saudi Arabia, Kuwait, United Arab Emirates and Iran reveal that 10–60% of mothers and 40–80% of their neonates had undetectable low 25(OH)D levels (0–25 nmol/L) at delivery.¹⁰⁶ Such low levels may be associated with poor maternal and neonatal outcomes, as has been documented in women from western countries. Indeed, Caucasian women with low 25(OH)D levels had a higher risk of pre-eclampsia and Cesarean sections, but we are unaware of any such studies in the ME or Asia.¹⁰⁶ More recently, children of women with low 25(OH)D levels in third term had smaller anthropometric parameters.¹⁰⁷ In Iran, neonates born to mothers with low 25(OH)D levels have lower cord 25(OH)D levels, and in one study were more likely to have lower birth weight, height, Apgar score and may be at risk for the development of rickets.¹⁰⁶ Unfortunately, the few studies conducted in the MENA were not population-based and thus not necessarily representative of vitamin D nutritional status of pregnant women and their neonates in the region. But the few studies available, revealed a 25(OH)D level below 20 ng/ml in mothers in all 6 studies and below 10 ng/ml in two of them and even lower levels in neonates and cord blood.¹⁰⁸^-¹¹² Predictors for low maternal 25(OH)D levels included dress code, winter season, dietary habits and avoidance of sun exposure.⁹²^,¹⁰⁸

Is There a Genetic Basis for Low Vitamin D Levels and Rickets in the MENA?

Lifestyle factors, namely sunlight exposure, diet and use of supplements, are well recognized major determinants of circulating 25(OH)D levels, in general,¹ including subjects from the MENA, as detailed above. Interestingly, it has been recently underscored that genetic factors may contribute up to 50% of inter-individual variability in serum 25(OH)D levels (Fig. 1).¹¹³ Several genetics determinants of vitamin D status were recently described in a large genome wide association study of over 30,000 individuals of European descent from 15 cohorts.¹¹⁴ In addition, single nucleotide polymorphisms (SNPs) at or near 6 pre-specified vitamin D pathways candidate genes were considered. These include the vitamin D receptor (VDR), 1-α-hydroxylase (CYP27B1), 25-hydroxylase (CYP2R1), 24-hydroxylase (CYP24A1), vitamin D binding protein (GC, DBP) and 27- and 25-hydroxylse (CYP27A1) genes. The discovered genetic polymorphisms included variants near genes involved in cholesterol synthesis (DHCR7), hydroxylation (CYP2R1 and CYP24A1) and vitamin D transport (GC), and these may identify individuals at high risk of vitamin D deficiency.¹¹⁴ African Americans are a subgroup at higher risk for low vitamin D levels. A recent study investigating associations between 94 three single nucleotide polymorphisms (SNPs) in 5 vitamin D pathway genes (GC, VDR, CYP2R1, CYP24A1, CYP27B1) and serum 25(OH)D in 379 African American and 379 Caucasian controls, revealed statistical associations for 3 SNPS, 2 in the vitamin D transport pathway and one in the hydroxylation pathway, only in African Americans.¹¹⁵ Loss of CYP2R1 was also shown to be associated with 25(OH)D deficiency in several families in Nigeria¹¹⁶^-¹¹⁸ and associations between VDR polymorphisms and rickets in subjects from the Middle East has also been previously raised.³¹^,¹¹⁹ In a retrospective study of 34 Saudi children above age 10 y, who presented with rickets to a major hospital in Riyadh between 1994–2000, 59% had vitamin D deficiency, 11% calcium deficiency, 3% renal failure and 27% genetic causes. Of the total, 12% were reported by authors to have hypophosphatemic rickets, 9% to have 25-hydroxylase deficiency and 6% to suffer from vitamin D dependent rickets type I.¹¹⁹ In addition, a recent report of 2 adolescent siblings from a Saudi family presenting with short stature and rickets, revealed 2 new mutations in CYP2R1.¹²⁰ The classical biochemical profile of very low 25(OH)D levels (below 4 ng/ml), within normal range calcitriol levels, the very high doses needed to normalize serum 25(OH)D levels, and an autosomal recessive inheritance pattern, had raised the author's suspicion for 25 hydroxylase deficiency. Residual hydroxylase function in the mutant allele or the presence of other hydroxylase enzymes that became more functional, in the presence of high levels of substrate, were proposed as possible mechanisms for the correction with supra-physiologic doses of vitamin D.¹²⁰

Figure 1. Serum 25(OH)D Levels in Adults (A) and Children (B) Based on Color Codes. The color codes are: green > 30 ng/ml, yellow 20–29 ng/ml, orange 10–19 ng/ml, and red < 10 ng/ml. To convert from ng/ml to nmol multiply by 2.5. The color codes were selected based on mean or median results from population based studies available or as obtained from most representative studies for each country. For countries with varying results, the color code was chosen as valid for ≥ 50% of reported values; or more than one color code was used (for, e.g., children in Iran).

In conclusion, there is a growing body of substantial evidence supporting a genetic basis for low 25(OH)D levels in several populations and some data for it in cases of rickets in the MENA, the latter is however based on small series and case reports. Thus the need for large scale population based genome wide association studies to adequately address this question in a definitive manner.

Impact of Vitamin D on Surrogate Markers or Major Health Outcomes in MENA

The evidence for a beneficial effect of vitamin D on musculoskeletal health and a potential effect on non-classical outcomes, such as cardiovascular diseases, diabetes, inflammatory, infectious, immune disorders and cancers, as well as mortality has been extensively reviewed,¹^,³^,⁵^,¹²¹^,¹²² and is beyond the scope of this paper. Cardiovascular diseases, maternal-neonatal health and infections are on the top of the health agenda of the World Health Organization and health authorities in countries worldwide, including the MENA region. Association and intervention studies evaluating the relationship between vitamin D and health outcomes, available to-date in the MENA region, will be examined here-in Table 4,⁶¹^,⁹⁴^,¹²³^-¹⁴⁰ and Table 5.¹⁰⁰^,¹⁴¹^-¹⁴⁹

Table 4. Overview on Association Studies Between 25(OH) D Levels and Health Outcomes in the Middle East and North Africa

Country	Author/Yr	Sampling Method City
Cases/ Controls N Gender/ Age	Assay type /Manufacturer	Exclusion criteria specified	Disease condition
/Health Outcomes	25(OH)D Level
Mean ng/ml	Association between 25(OH)D and outcome (Correlation)
Egypt	Olama et al.
2012¹²³	Clinic based
Cases: 50 ♀ 32.3 ± 9.4 y
Controls: 50 healthy ♀ 33.1 ± 9.7 y	ELISA/IDS	Yes	Fibromyalgia	Cases: 15.1 ± 6.1
Controls: 18.8 ± 5.4	Lumbar spine: r = -0.352
VAS of pain: r = -0.338
Beck score for depression: r = -0.328
	El Husseiny et al. 2012¹²⁴	Clinic based Cairo
Cases: 36♂, 14 ♀ 30–65 y
Controls:: 25 age- and gender-matched healthy subjects	RIA/Incstar	Yes	HCV infection	Cases: 15 ± 5.2
Controls: 39.7 ± 10.8	Cases:
Viral load: r = -0.84 IL-23: r = -0.776
IL-17: r = -0.665 MCP-1: r = -0.94
	Schaalan et al. 2012¹²⁵	Clinic based Cairo
Cases: 36♂, 14 ♀
Controls:: 25 age- and gender matched healthy subjects	RIA/Incstar	Yes	HCV infection	Cases: ♂10.30 ± 2.12
♀10.00 ± 2.60
Controls: 39.70 ± 10.80	Cases:
25(OH)D and IL-17: r = -0.679
1.25(OH)D and IL-17: r = -0.679
1.25(OH)D and IL-23: r = -0.801
	Hamza et al.
2011¹²⁶	Clinic, Hospital and university based Cairo
Cases: 52 ♀ and 8 ♂/ 6–19 y
Controls: 50 ♀, 10 ♂/ 7.2–18.5 y	ELISA/ VDBP	Yes	SLE	Cases: 26.33 ± 12.05
13% < 10 60% < 30 27% > 30
Controls: 42.66 ± 9.20	SLEDAI: r = -0.91
	Al Sayed
2007¹²⁷	Clinic based Cairo
Cases:93♂♀ 45.2 ± 2.6 y
Controls:70 healthy 47.1 ± 3.1 y	RIA/IDS	Yes	Metabolic syndrome	Cases: 16.2 ± 4.52
Control: 25 ± 4.48	Cases:
BMI: r = -0.684 HOMA: r = -0.395
HDL: r = 0.277 PTH: r = -0.235
S. Insulin:r = -0.396
Iran	Khalili et al.
2012¹²⁸	Hospital based Tehran
139 ♀ > 55 y, ♂ > 45 y	RIA/ Abcam pic	Yes	Acute Myocardial infarction	10.92 ± 7.2	Hypertension: OR = 2.92
Use of cardiovascular drugs: OR = 2.36
Survival: OR = 0.216
	Hosseinpanah et al. 2011¹²⁹	Population based Tehran
Cases: 251♂♀ 56.0 ± 10.6 y
Controls: 251 healthy subjects 56.7 ± 11.7 y	EIA/ DRG	Yes	Cardiovascular	Median
Cases: 12.5 (8.4–24.4)
Controls: 18.1 (11–31)	Vit D < 10 had an almost 3-fold higher risk of developing cardiovascular outcomes r^a = 2.90 than those between 10–15ng/ml r = 1.46
	Bonakdar et al. 2011¹³⁰	Clinic based Isfahan
40 ♀ 25.46 ± 4.16 y	RIA/ DIAsource	Yes	SLE	9.68 ± 0.84	BILAG: r = -0.486
BILAG after Adjustment: r^b = - 0.292
Low vit D higher titers of anti-dsDNA
	Heidari et al. 2010¹³¹	Clinic based Babol
Cases: 276 ♂♀ 44.3 ± 15 y
Controls: 202♂♀ 46.4 ± 14.2 y	ELISA/DRG	Yes	Musculoskeletal pain	Cases: 33.1 ± 28.4
Controls: 23.8 ± 29.1	Vit D < 20 vs. ≥ 20 with:
Musculoskeletal pain: OR^c = 2.95
Leg pain: OR^c = 7.4
Widespread pain: OR^c = 2.8
Arthralgia: OR^c = 3.9
	Garakyaraghi et al. 2010¹³²	Hospital based Isfahan
28 ♀, 67 ♂ 62 ± 11 y	CIA/Diasorin	Yes	Heart failure	56.78 ± 51.33	Diastolic volume: r = −0.24
Adjusted for age, Creatinine: r = −0.261
	Bonakkdaran et al. 2009¹³³	Hospital based Mashhad
119 ♂♀ 55.3 ± 11.2 y	RIA/Biosource	Yes	T2DM	32.4 ± 21.6	Age: r = -0.21, BMI: r = -0.25, CRP: r = -0.06
	Omrani et al. 2006¹³⁴	Cluster sampling Shiraz
676 healthy women aged 20–74 y	IRMA/ IDS	Yes	Mineral Metabolism	28.9 ± 23.0	PTH r = –0.10
Independent of age
Occupied Palestine/ Israel	Saliba et al.
2012¹³⁵	Population Based Clalit Health Services
Cases: 1180 ♂♀ 65.30 ± 13.52 y
Controls:184,479 ♂♀ 57.67 ± 18.25 y	CIA/DiaSorin	Yes	Primary Hyperparathyroidism	Cases: 19 ± 9
Controls: 20.8 ± 9.8	Cases:
PTH: r = −0.238 ALKPhos: r = −0.180 Calcium: r = −0.054
	Amital et al. 2010¹³⁶	278 with systemic lupus erythematosus activity (SLEDAI)
100 with European Lupus activity measurement (ECLAM) 40.2 ± 14.2 y	CIA/Diasorin	No	SLE	SLEDAI: 23.9 ± 14.0
ECLAM: 27.6 ± 13.9	Standardized values z-scores r = -0.12 The more active the disease, the lower the vitamin D concentration
Lebanon	Arabi et al.
2012⁹⁴	Population based Beirut
65 ♂and 130 ♀ 72.5 ± 5.1 y	RIA/ IDS	Yes	BMD
Mineral Metabolism	♂ 14.7 ± 4.0
♀ 14.6 ± 7.4	Overall:
% Change Trochanter BMD: r^d = 0.19
♂:% Change Total hip BMD: r^d = 0.31
% Change F. Neck BMD: r^d = 0.36
% Change Trochanter BMD r^d = 0.26
	Arabi et al.
2006⁶¹	Population based Beirut
286♀ 73.4 ± 5.2 y
157♂ 74.1 ± 5.08 y	RIA/ IDS	Yes	BMD
Mineral Metabolism		♀BMD Total hip, FN, Troch: r^e = 0.10–0.18
♂ BMD Total hip,spine, FN, Troch:r^e = 0.16 -0.27
Qatar	Bener et al.
2009¹³⁷	Clinics /Face to face Interviews Doha
Cases: 170 ♂♀ 10.5 ± 3.8 y
Controls: 170 ♂♀ 9.9 ± 4.2. yrs	RIA/DiaSorin	No	T1DM	Cases: 15.8 ± 9.2
Controls:18.5 ± 9.6	NA
Saudi Arabia	Bin –Abbas et al. 2011¹³⁸	Pediatric and Endo Clinics Riyadh
Cases:59 ♀ 41 ♂
Controls: 52♀ 48 ♂	HPLC	Yes	T1DM	Cases: 14.7 ± 5.7
Controls:17.9 ± 5.6	No Correlation between glycemic control and 25 OHD level.
	Al Daghri et al. 2010¹³⁹	Primary Health Care Centers Riyadh
Cases: 76 ♀, 88 ♂ 50.6 ± 10.1 y
Controls: 106 ♀, 71 ♂non-diabetic
37.5 ± 15.3 y	ELISA/ IDS	Yes	T2DM	Cases: 10.8 ± 4.7
Controls: 7.2 ± 2.9	Cases: TC: r = -0.20 LDL-C: r = -0.17
TG: r = -0.17 BMI: r = -0.22
Controls: SBP: r = 0.22 WHR: r = 0.16
Non-Adjusted values
Yemen	Salem et al.
2009¹⁴⁰	Hospital based Sana’a
152 children with VSP 2–59 mo	ELISA/ IDS	yes	Very severe pneumonia,
some with rickets	Deficient n = 50:37.2 ± 17.3
Sufficient n = 9: 47.3 ± 17.6	Failure to respond to antibiotic therapy in rachitic compared with non rachitic OR = 1.38

Only significantly different 25(OH)D levels between cases and controls, and correlations .Details on studies that presented adjusted correlations are as follows: Hosseinpahanh et al. 2011, r^a adjusted for BMI, FPG, SBP, DBP,CT,TG,HDL-C, Smoking Status, degree of physical activity, premature CVD familial history . Bonakdar et al. 2011, r^b adjusted for age, BMI, sun exposure, use of sunscreen, physical activity. Heidari et al. 2011, OR^c adjusted for sex. Arabi et al. 2012, r^c adjusted for age, calcium intake, serum Creatinine and PTH in multivariate models, mean 25OHD was no more a predictor of bone loss. Arabi et al. 2006, r^d adjusted for age, height, lean mass and PTH levels, 25OHD level did not have residual significant contribution to BMD at any skeletal site except the trochanter in men. Abbreviations in table listed here in alphabetical order: ALKPhos:Alkaline Phosphatase; BILAG: British Isles Lupus Assessment Group; BMD: Bone Mineral Density; BMI: Body Mass Index; CIA: Chemiluminescent Assay; CRP: C- Reactive Protein; DsDNA: Double Stranded DNA; EIA: Enzyme immunoassay; ELISA: Enzyme-linked immunosorbent Assay; ECLAM: European Consensus Lupus Activity Measurement; FN: Femoral Neck; HCV: Hepatitis C virus; HDL: High Density Lipoprotein; HOMA: Homeostasis Model Assessment ; HPLC: High-performance liquid chromatography; IDS: Immunodiagnostic Systems; IL-17: Interleukin-17; IL-23: Interleukin-23; IRMA: Immunoradiometric Assay; LDL-C: Low Density Lipoprotein- Cholesterol; MCP-1: Macrophage chemoattractant protein-1; NA: Not Available; OR: Odds Ratio; r: Correlation; RIA: Radioimmunoassay; SBP: Systolic Blood Pressure; SLE: Systemic Lupus Erythematosus; SLEDAI: Systemic Lupus Erythematosus Disease Activity Index; TC: Total Cholesterol; TG: Triglycerides ; Troch: Trochanter; T1DM: Type 1 Diabetes Mellitus; T2DM: Type 2 Diabetes Mellitus; Vit: Vitamin; VAS: Visual Analogue Scale; VSP: Very Severe Pneumonia; VDBP: Vitamin Tracer, for the Binding Pocket of Vitamin D Protein; WHR: Waist Hip Ratio; Yrs: Years

Table 5. Overview on Interventional Studies between 25(OH)D Levels and Health Outcomes in the Middle East

Country	Author
Yr	Sampling Method
City (Latitude)
N Gender/ Age	Protocol Design	Intervention
Type/Dose/Duration	Assay type/ Manufacturer	Exclusion criteria specified	25(OH)D Level Mean ng/ml	Effect on Health Outcome
Iran	Shakinba et al.
2011¹⁴¹	School Based
Yazd (32°N)
120 girls 12–15 y
Group 1: 28 with Vit D Deficiency
Group 2: 23 with Vit D Deficiency
Group 3: 30
Group 4: 30	RCT	Group 1: 300,000 IU D3 once,
randomized to 50,000IU D3/month
Group 2: 300,000 IU D3 once,
randomized to 100,000 IU D3/
3 mo
Group 3: 50,000 IU D3/3 mo
Group 4: 100,000 IU D3/3 mo	CIA/DiaSorin	No	Baseline One year
Group 1 29.7 ± 4.6 47% 20–30
53% 30–100
Group 2 30 ± 5.6 57% 20–30
43% 30–100
Group 3 15.2 ± 6 13% < 10
73% 10–20
11% 20–30
3% 30–100
Group 4 23 ± 6.8 45% 10–20
35% 20–30
19% 30–100	NA
	Ghazi et al.
2010¹⁴²	School Based
Tehran (35.7°N)
105 ♂, 105 ♀14–20 y 16 ± 1.5 y
Group A:35♂,35♀
Group B:34♂,35♀
Group C:34♂,35♀	Double-blinded RCT	Group A:50,000 IU D3/monthly
Group B: 50,000 IU D3/2 mo+ placebo every alternative month
Group C:Placebo	ELISA/IDS		Baseline 6 mo
Group A: 12.8 ± 8.8 ♀19.2 ± 9.4
♂29 ± 10.5
Group B: 11.3 ± 5.8 ♀13.5 ± 9.2
♂23.1 ± 7.6
Group C: 11.6 ± 7.2 ♀8 ± 5.6
♂15.6 ± 6.4	NA
Israel	Gotsman et al.
2012¹⁴³	Population based Clalit Health Services
A- 3009 ♂♀ with Heart Failure 75.9 ± 10.7 y
46,825♀♂ controls 64.7 ± 11.3 y
B- 791 ♂♀with Heart Failure
458 ♂♀ with supplementation
333 ♀♂without supplementation	A-Case-Control
B-Interventional	B. 800 IU/d and 1000 IU/d for median follow up of 518 d.	RIA/DiaSorin	No	A- Cases Median:14.8
Controls Median:16.3
B- Survival Rate
HF patients < 10 ng/ml with supplementation:85.6 ± 1.7%
HF patients < 10 ng/ml without supplementation:81.6 ± 1.7%	Reduced Mortality in Heart Failure patients HR = 1.52 and controls HR = 1.91
Lebanon	El-Hajj Fuleihan
et al 2006¹⁰⁰	School Based
Beirut (33°N)
179 ♀
Group A: 13 ± 2.1 y
Group B: 13.1 ± 2.2 y
Group C: 13.6 ± 2.1 y	Double-blinded RCT	Group A:Placebo
Group B: Low dose 200 IU D3/d
Group C: High dose 2000 IU D3/d	RIA/DiaSorin	Yes	Baseline One year
Group A: 14 ± 7 16 ± 8
Group B: 14 ± 9 17 ± 6
Group C: 14 ± 8 38 ± 31	Low dose and High dose: increase in BMD, Lean Mass
High dose:increase in Total BMD, Bone Area
Premenarcheal girls had the highest increment
Country	Author
Yr	Sampling Method
City (Latitude)
N Gender/ Age	Protocol Design	Intervention
Type/Dose/Duration	Assay type/ Manufacturer	Exclusion criteria specified	25(OH)D Level Mean ng/ml	Effect on Health Outcome
Qatar	Soliman et al. 2011¹⁴⁴	General Practitioner Clinic
Doha(25.3°N)
40 Adolescents with Vit D Deficiency	Prospective
Open-Label
Non-Randomized	600,000 IU D3 every 2–3 mo	RIA	No	Pre-Interv Post Interv
9.3 ± 4.6 27.7 ± 9.2	Healing of Rickets in all patients at one year.
Saudi Arabia	Al-Daghri et al.
2012¹⁴⁵	Primary Health Care Centers
Riyadh (24.6°N)
31♂28♀ 18–65 y 38 ± 14.1 y	Interventional	Advice for 5–30 min sun exposure twice/ week and vitamin-D rich foods	ELISA/IDS	Yes	Baseline 6 mo 12 mo
7.6 ± 0.6 10.7 ± 0.6 11.4 ± 0.6	Decrease of Metabolic Syndrome from 25% to 13%
UAE	Rajah et al.
2010¹⁴⁶	Hospital Based
Abu Dhabi (24°N)
10 Children with Rickets:
Group 1: 7 children
Group 2: 3 children
21.2 ± 8.4 mo	Retrospective
Audit	Group 1:2000 IU D2/d for 3 mo +400 IU D2/d subsequently+ Ca 40 mg/Kg/d for 3 mo
Group 2: stosstherapy 600,000IU D2 single dose + Ca 40 mg/Kg/d for 3 mo	HPLC	Yes	Baseline 3 mo
15.1 ± 10.3 NA
Median: 11.6 Median: 57.4	NA
	Saadi et al.
2009¹⁴⁷	Maternal-Child Health Clinic
Al-Ain(24°N)
Group 1: 22 mothers 28.1 ± 4.7 y
Group 2: 22 mothers 27.6 ± 6.5 y
Group 1: 22 infants 19.1 ± 25.4 d
Group 2: 24 infants 20.6 ± 22.9 d	RCT	Mothers:
Group 1:2000 IU D2/d for 3 mo
Group 2:60,000 IU D2/m for 3months
Infants:400 IU D2/d for 3 mo	RIA /DiaSorin	No	Mothers Pre-Interv Post Interv
Group 1: 11 ± 4 16.9 ± 5.6
Group 2: 8.9 ± 4 15 ± 4
Infants 30% < 20 ng/ml at 3 mo
Group 1: 5.6 ± 3.4 19.8 ± 7.4
Group 2: 5.5 ± 4.8 17.8 ± 6	NA
	Rajah et al.
2008¹⁴⁸	Hospital Based
Abu Dhabi (24°N)
31 Children with Rickets:
8 Vit D deficient 14.8 ± 3.2 mo
8 Ca deficient 19.8 ± 2.3 mo	Quasi-Experimental Non-Randomized	2000–5000 IU D2/d for 3 mo + 400 IU D2/d for a variable period	CIA/Nichols	No	Baseline:
8 Vit D deficient: 6.9 ± 1.3
8 Ca deficient: 17.7 ± 7.1	Height z-score
Entry: -1.74 Termination:-0.88
	Saadi et al.
2007¹⁴⁹	Maternal-Child Health Clinic
Al-Ain(24°N)
Group 1:45 lactating♀29.2 ± 5.5yrs
Group 2:45 lactating♀29.9 ± 6.7yrs
Group1:43nulliparous♀23 ± 5.2yrs
Group2:45nulliparous♀24.6 ± 5.1yrs	Open-Label
RCT	Group 1:2000 IU D2/d for 3 mo
Group 2:60,000 IU D2/m for 3months	RIA /DiaSorin	Yes	Lactating Pre-Interv Post-Interv
Group 1: 10.9 ± 4.2 17 ± 5.6
Group 2: 9.3 ± 4.3 15 ± 4.2
Nulliparous
Group 1: 7.8 ± 5 16.7 ± 10.6
Group 2: 7.6 ± 4.9 15.7 ± 8.6	1/3 ♀achieved 25(0H)D ≥ 20ng/ml

Abbreviations in table listed here in alphabetical order: BMD: Bone Mineral Density; Ca: Calcium; CIA: Chemiluminescent Assay; ELISA: Enzyme-linked immunosorbent Assay; HPLC: High-performance liquid chromatography; HR: Hazard Ratio; IDS: Immunodiagnostic Systems; NA: Not Available; RIA: Radioimmunoassay.

Associations studiesMusculoskeletal health
Significant negative associations between 25(OH)D and PTH levels were reported in young and old Lebanese subjects,⁶² adults and elderly subjects from Iran,¹³⁴^,¹⁵⁰ and patients with hyperparathyroidism from Israel.¹³⁵ Positive associations between 25(OH)D levels and bone mass were also reported at several skeletal sites, in adolescent Lebanese girls¹⁰⁰ and elderly subjects.⁶¹ In the elderly Lebanese, 25(OH)D levels also correlated with lean mass in men but not women and the correlations with BMD disappeared for all skeletal sites except for trochanter after adjusting for lean mass and PTH.⁶¹ In the same study, subjects were followed prospectively and25(OH)D levels significantly correlated with bone loss over a mean follow-up of 4.4 y. This relation disappeared after adjusting for PTH levels.⁹⁴ In the adolescent study, there were no significant relationships between VDR genotype and baseline bone mass BMD, but in the elderly study, elderly women with the heterozygous VDR genotype had the highest bone mass at the lumbar spine and forearm.¹⁵¹

Non-classical outcomes
Lower mean 25(OH)D levels were reported in patients with type I DM in Saudi Arabia and Qatar¹³⁷^,¹³⁸ and it has been suggested that low levels may also contribute to metabolic syndrome and type II DM.¹⁵² This is particularly pertinent, considering that the Middle East registers some of the highest rates for obesity, exceeding the rising tide in western countries, reaching 40–50%,¹⁵³ and has the greatest relative increase in diabetes prevalence, with rates reaching 20% in Bahrain, Saudi Arabia and the United Arab Emirates.¹⁵³^,¹⁵⁴ In patients with type II diabetes, negative correlations with BMI and several lipid parameters, were reported in studies from Iran and Saudi Arabia.¹³³^,¹³⁹ Mean 25(OH)D levels were also low in subjects with metabolic syndrome and also negatively correlated with BMI, lipid parameters, blood pressure and indices of insulin sensitivity.¹²⁷^,¹⁴⁵ The relationship between vitamin D and cardiovascular diseases and mortality has been intensely scrutinized in western populations,¹²² and examined in three studies from MENA (Table 4). In the Tehran Lipid Glucose study, subjects with 25(OH)D levels below 10 ng/ml, had an almost 3-fold higher risk of developing cardiovascular outcomes than those above 15 ng/ml.¹²⁹ In a small longitudinal study of 139 Iranian women admitted with acute myocardial infarction, 25(OH)D levels correlated with overall survival.¹²⁸ These findings were validated in large HMO population-based database from Israel, that demonstrated that patients with heart failure and 25(OH)D levels below 10 ng/ml, had an increased risk of mortality, HR 1.52 (95% CI 1.21−1.92) and that patients who took vitamin D, at doses of 800–1000 IU/day reduced mortality, HR = 0.68 (95% CI 0.54−0.85), at a median follow-up of 518 d.¹⁴³

Lower 25(OH)D levels have also been described in subjects with Systemic Lupus Erythematosis (SLE) and negative correlations reported with several indices of SLE disease activity in patients from Iran, Egypt and Israel.¹²⁶^,¹³⁰^,¹³⁶ Associations with other rheumatologic conditions, musculoskeletal pain and fibromyalgia have also been described in patients from Egypt and Iran.¹²³^,¹³¹ Mean 25(OH)D level was significantly lower in Egyptian patients with Hepatitis C Virus (HCV) infection than controls, measured at 10 ng/ml and negatively correlated with viral load and circulating levels of several interleukins.¹²⁴ Calcitriol also negatively correlated with interleukin levels in the same study subjects.¹²⁵ Lower 25(OH)D levels have also been noted in adults Iranian patients with multiple sclerosis,¹⁵⁵ and children suffering from Celiac Disease in Israel.¹⁵⁶ Only few are the studies that performed the necessary adjustments to identify the independent impact of vitamin D on health outcomes. Furthermore, association studies cannot control for all potential confounders and thus the lack of good evidence for a cause- effect relationship. For example obese subjects have low vitamin D and are also more likely to display the profile of metabolic syndrome, but that does not prove that low vitamin D is the cause for metabolic syndrome. Similarly, illnesses in general and cirrhosis in particular are conditions more likely to be associated with low vitamin D, but there is no good evidence for a causative effect for vitamin D in the illness. Thus there exists the need to rely on intervention studies, which are however scarce.

Intervention Studies

Rickets
A Cochrane review of four interventions trials enrolling around 1700 term infants, lasting between 9 mo and 2 y, showed that vitamin D at doses of 300−400 IU/day was sufficient to prevent rickets.¹⁵⁷

Various regimens to treat rickets in the region have been described and were mostly conducted in non-randomized, non-blinded interventional studies. Treatment with a single intramuscular injection of vitamin D at doses of 150,000–600,000 IU, single oral doses between 50,000 IU and 600, 000 IU, daily injections or oral doses of 5,000 to 20, 000 IU for 1–3 mo followed by 400 IU daily maintenance, all revealed substantial improvement in biochemical, clinical and radiological features of rickets.¹¹

In a dose ranging study of 52 Turkish infants with nutritional rickets and a mean age of 10 mo, subjects were randomized to receive one oral dose of vitamin D of 50,000 IU, 300,000 IU or 600,000 IU, and all received oral calcium for one week. On the 30th day there was no difference in the improvement between the three groups, and all patients had improved by the 60th day post-therapy, however, eight infants developed hypercalcemia, six of which were allocated to the high dose group.¹⁵⁸ The two most recent intervention studies conducted in ME are detailed in Table 5 and confirm findings from previous studies as summarized above. Children with rickets from some countries in ME such as Egypt, Saudi Arabia and the United Arab Emirates have low calcium intake. Therefore, careful assessment of calcium nutrition and concomitant therapy with calcium, in cases from the region is indicated and would expedite clinical recovery.

Skeletal health in adults
The relationship between 25(OH)D levels and indices of bone and mineral metabolism, based on randomized controlled trials, are well established and extensively studied in western populations and to a lesser extent in other ethnic groups.¹⁰⁶ There are no such studies on subjects in the MENA region.

Skeletal health in children and adolescents
The IOM report states that the Recommended Dietary Allowance (RDA) is the dose of vitamin D that would result in desirable 25(OH)D levels, above 20 ng/ml, in 97.5% of the population. . In children, the RDA is 600 IU/d.¹⁶Table 5 summarizes mean pre- and post-intervention 25(OH) D levels from recent studies in the region. The administration of doses of vitamin D, several folds above 600IU, fail to bring most subjects above the 20 ng/ml cut-off, presuming the same desirable level is needed across ethnic groups.

A recent meta-analysis of 6 randomized placebo controlled trials studies, concluded that it is unlikely that vitamin D supplements are beneficial to bone mass in subjects with normal 25 (OH)D levels.¹⁵⁹ However, planned subgroup analyses by baseline 25(OH)D level suggest that vitamin D supplementation of deficient children and adolescents could result in clinically useful improvements.¹⁵⁹ The latter was in large part driven by results from a randomized placebo controlled trial in 179 Lebanese girls, mean age 13 y, that showed a positive impact of vitamin D, administered weekly, at the equivalent daily doses of 200 IU and 2000 IU/day on musculoskeletal parameters in girls, including bone mineral content, density, area and lean mass, especially during the pre-menarcheal period.¹⁰⁰ A significant relationship between VDR genotypes and changes in bone mass at one year emerged and remained significant after adjustment for puberty, changes in lean mass, height and bone area.¹⁶⁰

Maternal and neonatal health
There are very few studies evaluating effect of vitamin D on musculoskeletal outcomes in mothers or neonates. In a randomized controlled vitamin D trial, conducted in 2000 neonates in India, vitamin D administration at 35 µg/day (1400IU/day), significantly increased standard deviation (Z) scores for weight, length and arm circumference and decreased the proportion of children with stunted growth at 6 mo, but had no effect on death, hospitalization, in or out-patient visits.¹⁶¹ Two on-going large multicenter trials, one conducted in US and the other in England, are evaluating the safety and efficacy of vitamin D administration, in pregnant mothers after the first term. The first uses doses of 400, 2000 to 4000 IU D /d until delivery,¹⁶² and the second 1000 IU cholecalciferol/d or Placebo from 14 weeks gestation until delivery.¹⁶³ Considering the severe vitamin D deficiency in pregnant and lactating women in MENA, the gap in this field is substantial.

Metabolic syndrome
A close examination of individual randomized controlled trials investigating the effect of vitamin D supplementation (± calcium) on components of the MetS reveals negative findings for most trials, with the exception of the few that used high doses of vitamin D in high-risk individuals with obesity and insulin resistance at entry, but none was conducted in MENA.¹⁵² In a study of 59 adult non diabetic, overweight and obese Saudis, advised to regularly expose themselves to sunlight and increase intake of vitamin D–rich foods, mean 25(OH)D levels increased from 7.6 to 11.2 ng/ml and the overall prevalence of MetS decreased from 25% to 13%, after one year.¹⁴⁵

Infections
Chronic infections are still prevalent in the MENA region. Strong associations between hypovitaminosis D and tuberculosis (TB) infection and acute lower respiratory tract infections have been reported in Indian, Turkish and Sub-Saharan African populations.¹⁰ Although 25(OH)D levels below 20 ng/ml were associated with increased susceptibility to active TB in HIV-uninfected (n = 196) and HIV-infected (n = 174) black Africans in Cape Town, South Africa,¹⁶⁴ vitamin D supplementation failed to improve clinical outcome or mortality in a randomized placebo controlled trial of 126 subjects recruited from National Health Service in United Kingdom with active TB.¹⁶⁵ Vitamin D did not significantly affect time to sputum culture conversion in the whole study population, but it did significantly hasten sputum culture conversion in participants with the tt genotype of the TaqI vitamin D receptor polymorphism.¹⁶⁵ However, vitamin D supplementation contributed to accelerating resolution of inflammatory responses and sputum smear conversion during tuberculosis treatment.¹⁶⁶

Conclusion

Reports of nutritional rickets and osteomalacia occur in the MENA region, despite its plentiful sunshine and at much higher rates than in western countries. Hypovitaminosis, defined as a serum 25(OH)D below 20 ng/ml, is also prevalent across populations throughout the lifecycle, with proportions varying for the most part between 30–90%, depending on gender, season and lifestyle pattern. Population based studies are scarce, but results available from such studies validate the above observations. Genetic polymorphisms along the vitamin D pathway have been described mostly in western populations. The extent to which they account for low 25 (OH)D levels in the region awaits population-based genome wide association studies. There are large information gaps on what may constitute a desirable level for various health outcomes for subjects from this region. Furthermore, the recommended vitamin D doses by the IOM and even ES are sub-optimal to bring 25(OH)D to the putative “desirable” level in various age groups. Thus the pressing need to address such knowledge gaps, in order to facilitate the development of evidence-based region specific guidelines and to impact this subclinical condition that may be at the root of several chronic diseases.

Disclosure of Potential Conflicts of Interest

No potential conflict of interest was disclosed.

Acknowledgments

The authors would like to thank Ms Aida Farha, Medical Information Specialist, Saab Medical Library, American University of Beirut, for her advice and assistance in designing comprehensive and complex searches of the various medical literature resources and for the provision of select articles and Mr. Samir Hanoun for the art work.

References

1. Holick MF. Vitamin D deficiency. N Engl J Med 2007; 357:266-81; PMID: 17634462; DOI: 10.1056/NEJMra070553.
2. Rosen CJ. Clinical practice. Vitamin D insufficiency. N Engl J Med 2011; 364:248-54; PMID: 21247315; DOI: 10.1056/NEJMcp1009570.
3. Lips P, van Schoor NM. The effect of vitamin D on bone and osteoporosis. Best Pract Res Clin Endocrinol Metab 2011; 25:585-91; PMID: 21872800; DOI: 10.1016/j.beem.2011.05.002.
4. Norman AW, Bouillon R. Vitamin D nutritional policy needs a vision for the future. Exp Biol Med (Maywood) 2010; 235:1034-45; PMID: 20667908; DOI: 10.1258/ebm.2010.010014.
5. Bouillon R, Bischoff-Ferrari H, Willett W. Vitamin D and health: perspectives from mice and man. J Bone Miner Res 2008; 23:974-9; PMID: 18442312; DOI: 10.1359/jbmr.080420.
6. Zittermann A, Iodice S, Pilz S, Grant WB, Bagnardi V, Gandini S. Vitamin D deficiency and mortality risk in the general population: a meta-analysis of prospective cohort studies. Am J Clin Nutr 2012; 95:91-100; PMID: 22170374; DOI: 10.3945/ajcn.111.014779.
7. Prentice A. Vitamin D deficiency: a global perspective. Nutr Rev 2008; 66:S153-64; PMID: 18844843; DOI: 10.1111/j.1753-4887.2008.00100.x.
8. Prentice A. Nutritional rickets around the world. J Steroid Biochem Mol Biol 2012; ; PMID: 23220549; DOI: 10.1016/j.jsbmb.2012.11.018.
9. El-Kaissi S, Sherbeeni S. “Vitamin D Deficiency in the Middle East and Its Health Consequences for Adults. Nutr Health” in Vitamin D: Physiology, Molecular Biology, and Clinical Applications, ed. Michael Holick. New York (NY): Humana Press; 2010.
10. Arabi A, El Rassi R, El-Hajj Fuleihan G. Hypovitaminosis D in developing countries-prevalence, risk factors and outcomes. Nat Rev Endocrinol 2010; 6:550-61; PMID: 20852586; DOI: 10.1038/nrendo.2010.146.
11. El-Hajj Fuleihan G. Vitamin D Deficiency in the Middle East and its Health Consequences. Clin Rev Bone and Min Met 2009; 7:77-93; DOI: 10.1007/s12018-009-9027-9.
12. Mithal A, Wahl DA, Bonjour JP, Burckhardt P, Dawson-Hughes B, Eisman JA, et al. Global vitamin D status and determinants of hypovitaminosis D. Osteoporos Int 2009; 20:1807-20; PMID: 19543765; DOI: 10.1007/s00198-009-0954-6.
13. van Schoor NM, Lips P. Worldwide vitamin D status. Best Pract Res Clin Endocrinol Metab 2011; 25:671-80; PMID: 21872807; DOI: 10.1016/j.beem.2011.06.007.
14. Wahl DA, Cooper C, Ebeling PR, Eggersdorfer M, Hilger J, Hoffmann K, et al. A global representation of vitamin D status in healthy populations. Arch Osteoporos 2012; 7:155-72; PMID: 23225293; DOI: 10.1007/s11657-012-0093-0.
15. Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, Heaney RP, et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2011; 96:1911-30; PMID: 21646368; DOI: 10.1210/jc.2011-0385.
16. Ross AC, Manson JE, Abrams SA, Aloia JF, Brannon PM, Clinton SK, et al. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. J Clin Endocrinol Metab 2011; 96:53-8; PMID: 21118827; DOI: 10.1210/jc.2010-2704.
17. www.unicef.org
18. www.worldbank.org
19. www.iofbonehealth.org
20. Barake M, Daher RT, Salti I, Cortas NK, Al-Shaar L, Habib RH, et al. 25-hydroxyvitamin D assay variations and impact on clinical decision making. J Clin Endocrinol Metab 2012; 97:835-43; PMID: 22238386; DOI: 10.1210/jc.2011-2584.
21. Sempos CT, Vesper HW, Phinney KW, Thienpont LM, Coates PM. Vitamin D status as an international issue: national surveys and the problem of standardization. Scand J Clin Lab Invest Suppl 2012; 243:32-40; PMID: 22536760.
22. Dawodu A, Agarwal M, Sankarankutty M, Hardy D, Kochiyil J, Badrinath P. Higher prevalence of vitamin D deficiency in mothers of rachitic than nonrachitic children. J Pediatr 2005; 147:109-11; PMID: 16027707; DOI: 10.1016/j.jpeds.2005.03.001.
23. Al-Atawi MS, Al-Alwan IA, Al-Mutair AN, Tamim HM, Al-Jurayyan NA. Epidemiology of nutritional rickets in children. Saudi J Kidney Dis Transpl 2009; 20:260-5; PMID: 19237815.
24. Al-Mustafa ZH, Al-Madan M, Al-Majid HJ, Al-Muslem S, Al-Ateeq S, Al-Ali AK. Vitamin D deficiency and rickets in the Eastern Province of Saudi Arabia. Ann Trop Paediatr 2007; 27:63-7; PMID: 17469734; DOI: 10.1179/146532807X170529.
25. Narchi H, El Jamil M, Kulaylat N. Symptomatic rickets in adolescence. Arch Dis Child 2001; 84:501-3; PMID: 11369569; DOI: 10.1136/adc.84.6.501.
26. Soliman AT, El-Dabbagh M, Adel A, Al Ali M, Aziz Bedair EM, Elalaily RK. Clinical responses to a mega-dose of vitamin D3 in infants and toddlers with vitamin D deficiency rickets. J Trop Pediatr 2010; 56:19-26; PMID: 19506025; DOI: 10.1093/tropej/fmp040.
27. Najada AS, Habashneh MS, Khader M. The frequency of nutritional rickets among hospitalized infants and its relation to respiratory diseases. J Trop Pediatr 2004; 50:364-8; PMID: 15537725; DOI: 10.1093/tropej/50.6.364.
28. Majid Molla A, Badawi MH, al-Yaish S, Sharma P, el-Salam RS, Molla AM. Risk factors for nutritional rickets among children in Kuwait. Pediatr Int 2000; 42:280-4; PMID: 10881586; DOI: 10.1046/j.1442-200x.2000.01230.x.
29. Baroncelli GI, Bereket A, El Kholy M, Audì L, Cesur Y, Ozkan B, et al. Rickets in the Middle East: role of environment and genetic predisposition. J Clin Endocrinol Metab 2008; 93:1743-50; PMID: 18285415; DOI: 10.1210/jc.2007-1413.
30. Dahifar H, Faraji A, Yassobi S, Ghorbani A. Asymptomatic rickets in adolescent girls. Indian J Pediatr 2007; 74:571-5; PMID: 17595501; DOI: 10.1007/s12098-007-0095-x.
31. Rajah J, Jubeh JA, Haq A, Shalash A, Parsons H. Nutritional rickets and z scores for height in the United Arab Emirates: to D or not to D?. Pediatr Int 2008; 50:424-8; PMID: 18937749; DOI: 10.1111/j.1442-200X.2008.02700.x.
32. Plotnikoff GA, Quigley JM. Prevalence of severe hypovitaminosis D in patients with persistent, nonspecific musculoskeletal pain. Mayo Clin Proc 2003; 78:1463-70; PMID: 14661675; DOI: 10.4065/78.12.1463.
33. Holick MF. Vitamin D deficiency: what a pain it is. Mayo Clin Proc 2003; 78:1457-9; PMID: 14661673; DOI: 10.4065/78.12.1457.
34. Priemel M, von Domarus C, Klatte TO, Kessler S, Schlie J, Meier S, et al. Bone mineralization defects and vitamin D deficiency: histomorphometric analysis of iliac crest bone biopsies and circulating 25-hydroxyvitamin D in 675 patients. J Bone Miner Res 2010; 25:305-12; PMID: 19594303; DOI: 10.1359/jbmr.090728.
35. Ballane GT, Sfeir JG, Dakik HA, Brown EM, El-Hajj Fuleihan G. Use of recombinant human parathyroid hormone in hypocalcemic cardiomyopathy. Eur J Endocrinol 2012; 166:1113-20; PMID: 22430263; DOI: 10.1530/EJE-11-1094.
36. Ukinc K. Severe osteomalacia presenting with multiple vertebral fractures: a case report and review of the literature. Endocrine 2009; 36:30-6; PMID: 19543841; DOI: 10.1007/s12020-009-9209-8.
37. Al-Ali H, Fuleihan GE. Nutritional osteomalacia: substantial clinical improvement and gain in bone density posttherapy. J Clin Densitom 2000; 3:97-101; PMID: 10745306; DOI: 10.1385/JCD:3:1:097.
38. Sedrani SH. Low 25-hydroxyvitamin D and normal serum calcium concentrations in Saudi Arabia: Riyadh region. Ann Nutr Metab 1984; 28:181-5; PMID: 6610383; DOI: 10.1159/000176801.
39. Baradaran A, Behradmanesh S, Nasri H. Association of body mass index and serum vitamin D level in healthy Iranian adolescents. Endokrynol Pol 2012; 63:29-33; PMID: 22378095.
40. Kashi Z, Saeedian Fs, Akha O, Gorgi Ma, Emadi Sf, Zakeri H. Vitamin D deficiency prevalence in summer compared to winter in a city with high humidity and a sultry climate. Endokrynol Pol 2011; 62:249-51; PMID: 21717408.
41. Hovsepian S, Amini M, Aminorroaya A, Amini P, Iraj B. Prevalence of vitamin D deficiency among adult population of Isfahan City, Iran. J Health Popul Nutr 2011; 29:149-55; PMID: 21608424; DOI: 10.3329/jhpn.v29i2.7857.
42. Kaykhaei MA, Hashemi M, Narouie B, Shikhzadeh A, Rashidi H, Moulaei N, et al. High prevalence of vitamin D deficiency in Zahedan, southeast Iran. Ann Nutr Metab 2011; 58:37-41; PMID: 21304235; DOI: 10.1159/000323749.
43. Hosseinpanah F, Pour SH, Heibatollahi M, Moghbel N, Asefzade S, Azizi F. The effects of air pollution on vitamin D status in healthy women: a cross sectional study. BMC Public Health 2010; 10:519; PMID: 20799984; DOI: 10.1186/1471-2458-10-519.
44. Maddah M, Sharami SH, Neyestani TR. Vitamin D insufficiency among postmenopausal women in urban and rural areas in Guilan, Northern Iran. J Nutr Elder 2009; 28:386-93; PMID: 21184380; DOI: 10.1080/01639360903393523.
45. Masoompour SM, Sadegholvaad A, Larijani B, Ranjbar-Omrani G. Effects of age and renal function on vitamin D status in men. Arch Iran Med 2008; 11:377-81; PMID: 18588368.
46. Hosseinpanah F, Rambod M, Hossein-nejad A, Larijani B, Azizi F. Association between vitamin D and bone mineral density in Iranian postmenopausal women. J Bone Miner Metab 2008; 26:86-92; PMID: 18095069; DOI: 10.1007/s00774-007-0791-7.
47. Hashemipour S, Larijani B, Adibi H, Sedaghat M, Pajouhi M, Bastan-Hagh MH, et al. The status of biochemical parameters in varying degrees of vitamin D deficiency. J Bone Miner Metab 2006; 24:213-8; PMID: 16622734; DOI: 10.1007/s00774-005-0674-8.
48. Rassouli A, Milanian I, Moslemi-Zadeh M. Determination of serum 25-hydroxyvitamin D(3) levels in early postmenopausal Iranian women: relationship with bone mineral density. Bone 2001; 29:428-30; PMID: 11704493; DOI: 10.1016/S8756-3282(01)00591-9.
49. Saliba W, Barnett-Griness O, Rennert G. The relationship between obesity and the increase in serum 25(OH)D levels in response to vitamin D supplementation. Osteoporos Int 2013; 24:1447-54; PMID: 22955311; DOI: 10.1007/s00198-012-2129-0.
50. Saliba W, Barnett O, Stein N, Kershenbaum A, Rennert G. The longitudinal variability of serum 25(OH)D levels. Eur J Intern Med 2012; 23:e106-11; PMID: 22560393; DOI: 10.1016/j.ejim.2012.02.002.
51. Saliba W, Barnett O, Rennert HS, Rennert G. The risk of all-cause mortality is inversely related to serum 25(OH)D levels. J Clin Endocrinol Metab 2012; 97:2792-8; PMID: 22648653; DOI: 10.1210/jc.2012-1747.
52. Tsur A, Metzger M, Dresner-Pollak R. Effect of different dress style on vitamin D level in healthy young Orthodox and ultra-Orthodox students in Israel. Osteoporos Int 2011; 22:2895-8; PMID: 21110005; DOI: 10.1007/s00198-010-1492-y.
53. Saliba W, Barnett O, Rennert HS, Lavi I, Rennert G. The relationship between serum 25(OH)D and parathyroid hormone levels. Am J Med 2011; 124:1165-70; PMID: 22114830; DOI: 10.1016/j.amjmed.2011.07.009.
54. Steinvil A, Leshem-Rubinow E, Berliner S, Justo D, Finn T, Ish-shalom M, et al. Vitamin D deficiency prevalence and cardiovascular risk in Israel. Eur J Clin Invest 2011; 41:263-8; PMID: 20955219; DOI: 10.1111/j.1365-2362.2010.02403.x.
55. Oren Y, Shapira Y, Agmon-Levin N, Kivity S, Zafrir Y, Altman A, et al. Vitamin D insufficiency in a sunny environment: a demographic and seasonal analysis. Isr Med Assoc J 2010; 12:751-6; PMID: 21348404.
56. Nichols EK, Khatib IM, Aburto NJ, Sullivan KM, Scanlon KS, Wirth JP, et al. Vitamin D status and determinants of deficiency among non-pregnant Jordanian women of reproductive age. Eur J Clin Nutr 2012; 66:751-6; PMID: 22415337; DOI: 10.1038/ejcn.2012.25.
57. Batieha A, Khader Y, Jaddou H, Hyassat D, Batieha Z, Khateeb M, et al. Vitamin D status in Jordan: dress style and gender discrepancies. Ann Nutr Metab 2011; 58:10-8; PMID: 21252499; DOI: 10.1159/000323097.
58. Mallah E, Hamad M, Elmanaseer M, Qinna N, Idkaidek N, Arafat T, et al. Plasma concentration of 25-hydroxyvitamin D among Jordanians: Effect of biological and habitual factors on vitamin D status. Bio Med Central Clin Path 2011; 11:8.
59. Mishal AA. Effects of different dress styles on vitamin D levels in healthy young Jordanian women. Osteoporos Int 2001; 12:931-5; PMID: 11804019; DOI: 10.1007/s001980170021.
60. Gannagé-Yared MH, Maalouf G, Khalife S, Challita S, Yaghi Y, Ziade N, et al. Prevalence and predictors of vitamin D inadequacy amongst Lebanese osteoporotic women. Br J Nutr 2009; 101:487-91; PMID: 18631414; DOI: 10.1017/S0007114508023404.
61. Arabi A, Baddoura R, Awada H, Salamoun M, Ayoub G, El-Hajj Fuleihan G. Hypovitaminosis D osteopathy: is it mediated through PTH, lean mass, or is it a direct effect?. Bone 2006; 39:268-75; PMID: 16495164; DOI: 10.1016/j.bone.2006.01.140.
62. Arabi A, Baddoura R, El-Rassi R, El-Hajj Fuleihan G. Age but not gender modulates the relationship between PTH and vitamin D. Bone 2010; 47:408-12; PMID: 20452474; DOI: 10.1016/j.bone.2010.05.002.
63. Gannagé-Yared MH, Chemali R, Yaacoub N, Halaby G. Hypovitaminosis D in a sunny country: relation to lifestyle and bone markers. J Bone Miner Res 2000; 15:1856-62; PMID: 10977006; DOI: 10.1359/jbmr.2000.15.9.1856.
64. Ardawi MS, Sibiany AM, Bakhsh TM, Qari MH, Maimani AA. High prevalence of vitamin D deficiency among healthy Saudi Arabian men: relationship to bone mineral density, parathyroid hormone, bone turnover markers, and lifestyle factors. Osteoporos Int 2012; 23:675-86; PMID: 21625888; DOI: 10.1007/s00198-011-1606-1.
65. Elshafie DE, Al-Khashan HI, Mishriky AM. Comparison of vitamin D deficiency in Saudi married couples. Eur J Clin Nutr 2012; 66:742-5; PMID: 22415335; DOI: 10.1038/ejcn.2012.29.
66. Kanan RM, Al Saleh YM, Fakhoury HM, Adham M, Aljaser S, Tamimi W. Year-round vitamin D deficiency among Saudi female out-patients. Public Health Nutr 2013; 16:544-8; PMID: 22691699; DOI: 10.1017/S1368980012002947.
67. Ardawi MS, Qari MH, Rouzi AA, Maimani AA, Raddadi RM. Vitamin D status in relation to obesity, bone mineral density, bone turnover markers and vitamin D receptor genotypes in healthy Saudi pre- and postmenopausal women. Osteoporos Int 2011; 22:463-75; PMID: 20431993; DOI: 10.1007/s00198-010-1249-7.
68. Alissa EM, Qadi SG, Alhujaili NA, Alshehri AM, Ferns GA. Effect of diet and lifestyle factors on bone health in postmenopausal women. J Bone Miner Metab 2011; 29:725-35; PMID: 21594583; DOI: 10.1007/s00774-011-0274-8.
69. Sadat-Ali M, Al Elq AH, Al-Turki HA, Al-Mulhim FA, Al-Ali AK. Influence of vitamin D levels on bone mineral density and osteoporosis. Ann Saudi Med 2011; 31:602-8; PMID: 22048506; DOI: 10.4103/0256-4947.87097.
70. Elsammak MY, Al-Wossaibi AA, Al-Howeish A, Alsaeed J. High prevalence of vitamin D deficiency in the sunny Eastern region of Saudi Arabia: a hospital-based study. East Mediterr Health J 2011; 17:317-22; PMID: 22259890.
71. Elsammak MY, Al-Wosaibi AA, Al-Howeish A, Alsaeed J. Vitamin d deficiency in Saudi Arabs. Horm Metab Res 2010; 42:364-8; PMID: 20213587; DOI: 10.1055/s-0030-1248296.
72. Al-Elq AH, Sadat-Ali M, Al-Turki HA, Al-Mulhim FA, Al-Ali AK. Is there a relationship between body mass index and serum vitamin D levels?. Saudi Med J 2009; 30:1542-6; PMID: 19936417.
73. Sadat-Ali M, AlElq A, Al-Turki H, Al-Mulhim F, Al-Ali A. Vitamin D levels in healthy men in eastern Saudi Arabia. Ann Saudi Med 2009; 29:378-82; PMID: 19700896; DOI: 10.4103/0256-4947.55168.
74. Al-Turki HA, Sadat-Ali M, Al-Elq AH, Al-Mulhim FA, Al-Ali AK. 25-Hydoxyvitamin D levels among healthy Saudi Arabian women. Saudi Med J 2008; 29:1765-8; PMID: 19082230.
75. Al Anouti F, Thomas J, Abdel-Wareth L, Rajah J, Grant WB, Haq A. Vitamin D deficiency and sun avoidance among university students at Abu Dhabi, United Arab Emirates. Dermatoendocrinol 2011; 3:235-9; PMID: 22259650; DOI: 10.4161/derm.3.4.16881.
76. Dawodu A, Kochiyil J, Altaye N. Pilot study of sunlight exposure and vitamin D status in Arab women of childbearing age. East Mediterr Health J 2011; 17:570-4; PMID: 21972479.
77. Saadi HF, Nagelkerke N, Benedict S, Qazaq HS, Zilahi E, Mohamadiyeh MK, et al. Predictors and relationships of serum 25 hydroxyvitamin D concentration with bone turnover markers, bone mineral density, and vitamin D receptor genotype in Emirati women. Bone 2006; 39:1136-43; PMID: 16814623; DOI: 10.1016/j.bone.2006.05.010.
78. El Maghraoui A, Ouzzif Z, Mounach A, Rezqi A, Achemlal L, Bezza A, et al. Hypovitaminosis D and prevalent asymptomatic vertebral fractures in Moroccan postmenopausal women. BMC Womens Health 2012; 12:11; PMID: 22531050; DOI: 10.1186/1472-6874-12-11.
79. Allali F, El Aichaoui S, Khazani H, Benyahia B, Saoud B, El Kabbaj S, et al. High prevalence of hypovitaminosis D in Morocco: relationship to lifestyle, physical performance, bone markers, and bone mineral density. Semin Arthritis Rheum 2009; 38:444-51; PMID: 18336870; DOI: 10.1016/j.semarthrit.2008.01.009.
80. Bahlous A, Farjallah N, Bouzid K, Klouz A, Mohsni A, Sahli H, et al. Hypovitaminosis D in Tunisian osteoporotic postmenopausal women and the relationship with bone fractures. Tunis Med 2009; 87:188-90; PMID: 19537011.
81. Meddeb N, Sahli H, Chahed M, Abdelmoula J, Feki M, Salah H, et al. Vitamin D deficiency in Tunisia. Osteoporos Int 2005; 16:180-3; PMID: 15197539; DOI: 10.1007/s00198-004-1658-6.
82. Al-Othman A, Al-Musharaf S, Al-Daghri NM, Krishnaswamy S, Yusuf DS, Alkharfy KM, et al. Effect of physical activity and sun exposure on vitamin D status of Saudi children and adolescents. BMC Pediatr 2012; 12:92; PMID: 22759399; DOI: 10.1186/1471-2431-12-92.
83. El-Hajj Fuleihan G, Nabulsi M, Choucair M, Salamoun M, Hajj Shahine C, Kizirian A, et al. Hypovitaminosis D in healthy schoolchildren. Pediatrics 2001; 107:E53; PMID: 11335774; DOI: 10.1542/peds.107.4.e53.
84. Moussavi M, Heidarpour R, Aminorroaya A, Pournaghshband Z, Amini M. Prevalence of vitamin D deficiency in Isfahani high school students in 2004. Horm Res 2005; 64:144-8; PMID: 16192739; DOI: 10.1159/000088588.
85. Al-Ghamdi MA, Lanham-New SA, Kahn JA. Differences in vitamin D status and calcium metabolism in Saudi Arabian boys and girls aged 6 to 18 years: effects of age, gender, extent of veiling and physical activity with concomitant implications for bone health. Public Health Nutr 2012; 15:1845-53; PMID: 22348990; DOI: 10.1017/S1368980011003612.
86. Neyestani TR, Hajifaraji M, Omidvar N, Eshraghian MR, Shariatzadeh N, Kalayi A, et al. High prevalence of vitamin D deficiency in school-age children in Tehran, 2008: a red alert. Public Health Nutr 2012; 15:324-30; PMID: 21356149; DOI: 10.1017/S1368980011000188.
87. Olang B, Naghavi M, Bastani D, Strandvik B, Yngve A. Optimal vitamin A and suboptimal vitamin D status are common in Iranian infants. Acta Paediatr 2011; 100:439-44; PMID: 20950411; DOI: 10.1111/j.1651-2227.2010.02058.x.
88. Abdul-Razzak KK, Ajlony MJ, Khoursheed AM, Obeidat BA. Vitamin D deficiency among healthy infants and toddlers: a prospective study from Irbid, Jordan. Pediatr Int 2011; 53:839-45; PMID: 21507148; DOI: 10.1111/j.1442-200X.2011.03388.x.
89. Razzaghy-Azar M, Shakiba M. Assessment of vitamin D status in healthy children and adolescents living in Tehran and its relation to iPTH, gender, weight and height. Ann Hum Biol 2010; 37:692-701; PMID: 20166840; DOI: 10.3109/03014460903527348.
90. Dawodu A, Agarwal M, Hossain M, Kochiyil J, Zayed R. Hypovitaminosis D and vitamin D deficiency in exclusively breast-feeding infants and their mothers in summer: a justification for vitamin D supplementation of breast-feeding infants. J Pediatr 2003; 142:169-73; PMID: 12584539; DOI: 10.1067/mpd.2003.63.
91. Ardestani PM, Salek M, Keshteli AH, Nejadnik H, Amini M, Hosseini SM, et al. Vitamin D status of 6- to 7-year-old children living in Isfahan, Iran. Endokrynol Pol 2010; 61:377-82; PMID: 20806182.
92. Narchi H, Kochiyil J, Zayed R, Abdulrazzak W, Agarwal M. Maternal vitamin D status throughout and after pregnancy. J Obstet Gynaecol 2010; 30:137-42; PMID: 20143971; DOI: 10.3109/01443610903315652.
93. Ghergherechi R, Hazhir N, Tabrizi A. Comparison of vitamin D deficiency and secondary hyperparathyroidism in obese and non-obese children and adolescents. Pak J Biol Sci 2012; 15:147-51; PMID: 22866545; DOI: 10.3923/pjbs.2012.147.151.
94. Arabi A, Baddoura R, El-Rassi R, El-Hajj Fuleihan G. PTH level but not 25 (OH) vitamin D level predicts bone loss rates in the elderly. Osteoporos Int 2012; 23:971-80; PMID: 21656018; DOI: 10.1007/s00198-011-1659-1.
95. van der Meer IM, Middelkoop BJ, Boeke AJ, Lips P. Prevalence of vitamin D deficiency among Turkish, Moroccan, Indian and sub-Sahara African populations in Europe and their countries of origin: an overview. Osteoporos Int 2011; 22:1009-21; PMID: 20461360; DOI: 10.1007/s00198-010-1279-1.
96. Moreno-Reyes R, Carpentier YA, Boelaert M, El Moumni K, Dufourny G, Bazelmans C, et al. Vitamin D deficiency and hyperparathyroidism in relation to ethnicity: a cross-sectional survey in healthy adults. Eur J Nutr 2009; 48:31-7; PMID: 19030910; DOI: 10.1007/s00394-008-0756-1.
97. Jazar A, Takruri H, Khuri-Bulos N. Vitamin D status in a sample of preschool children aged from 1 to 6 years visiting the pediatrics clinic at Jordan University hospital. J Med J 2011; 45:308-16.
98. Gharaibeh MA, Stoecker BJ. Assessment of serum 25(OH)D concentration in women of childbearing age and their preschool children in Northern Jordan during summer. Eur J Clin Nutr 2009; 63:1320-6; PMID: 19707220; DOI: 10.1038/ejcn.2009.99.
99. El-Hajj Fuleihan G, Vieth R. Vitamin D insufficiency and musculoskeletal health in children and adolescents. International Congress Series 2007; 1297:91-108.
100. El-Hajj Fuleihan G, Nabulsi M, Tamim H, Maalouf J, Salamoun M, Khalife H, et al. Effect of vitamin D replacement on musculoskeletal parameters in school children: a randomized controlled trial. J Clin Endocrinol Metab 2006; 91:405-12; PMID: 16278262; DOI: 10.1210/jc.2005-1436.
101. Rajah J, Haq A, Pettifor JM. Vitamin D and calcium status in urban children attending an ambulatory clinic service in the United Arab Emirates. Dermatoendocrinol 2012; 4:39-43; PMID: 22870351; DOI: 10.4161/derm.18250.
102. Kensarah O, Azzeh F, Vitamin D. Status of Healthy School Children from Western Saudi Arabia. Pakistan Journal of Nutrition 2012; 11:288-92; DOI: 10.3923/pjn.2012.288.292.
103. Bener A, Al-Ali M, Hoffmann GF. Vitamin D deficiency in healthy children in a sunny country: associated factors. Int J Food Sci Nutr 2009; 60:60-70; PMID: 18946796; DOI: 10.1080/09637480802400487.
104. Dawodu A, Dawson KP, Amirlak I, Kochiyil J, Agarwal M, Badrinath P. Diet, clothing, sunshine exposure and micronutrient status of Arab infants and young children. Ann Trop Paediatr 2001; 21:39-44; PMID: 11284245; DOI: 10.1080/02724930020028902.
105. Racinais S, Hamilton B, Li CK, Grantham J. Vitamin D and physical fitness in Qatari girls. Arch Dis Child 2010; 95:854-5; PMID: 20554768; DOI: 10.1136/adc.2009.163238.
106. El-Hajj Fuleihan G, Rahme M, Bassil D. Do Desirable Vitamin D Levels Vary Globally? In: Burckhardt P, Dawson-Hughes B, and Weaver C, eds. Nutritional Influences on Bone Health – 8th International Symposium. Springer Science publisher, 2012 (In Press).
107. Gernand AD, Simhan HN, Klebanoff MA, Bodnar LM. Maternal serum 25-hydroxyvitamin D and measures of newborn and placental weight in a U.S. multicenter cohort study. J Clin Endocrinol Metab 2013; 98:398-404; PMID: 23162094; DOI: 10.1210/jc.2012-3275.
108. Kazemi A, Sharifi F, Jafari N, Mousavinasab N. High prevalence of vitamin D deficiency among pregnant women and their newborns in an Iranian population. J Womens Health (Larchmt) 2009; 18:835-9; PMID: 19514825; DOI: 10.1089/jwh.2008.0954.
109. Asemi Z, Taghizadeh M, Sarahroodi S, Jazayeri S, Tabasi Z, Seyyedi F. Assessment of the relationship of vitamin D with serum antioxidant vitamins E and A and their deficiencies in Iranian pregnant women. Saudi Med J 2010; 31:1119-23; PMID: 20953527.
110. Bassir M, Laborie S, Lapillonne A, Claris O, Chappuis MC, Salle BL. Vitamin D deficiency in Iranian mothers and their neonates: a pilot study. Acta Paediatr 2001; 90:577-9; PMID: 11430721; DOI: 10.1111/j.1651-2227.2001.tb00802.x.
111. Mukamel MN, Weisman Y, Somech R, Eisenberg Z, Landman J, Shapira I, et al. Vitamin D deficiency and insufficiency in Orthodox and non-Orthodox Jewish mothers in Israel. Isr Med Assoc J 2001; 3:419-21; PMID: 11433634.
112. Molla AM, Al Badawi M, Hammoud MS, Molla AM, Shukkur M, Thalib L, et al. Vitamin D status of mothers and their neonates in Kuwait. Pediatr Int 2005; 47:649-52; PMID: 16354218; DOI: 10.1111/j.1442-200x.2005.02141.x.
113. Shea MK, Benjamin EJ, Dupuis J, Massaro JM, Jacques PF, D’Agostino RB, et al. Genetic and non-genetic correlates of vitamins K and D. Eur J Clin Nutr 2009; 63:458-64; PMID: 18030310; DOI: 10.1038/sj.ejcn.1602959.
114. Wang TJ, Zhang F, Richards JB, Kestenbaum B, van Meurs JB, Berry D, et al. Common genetic determinants of vitamin D insufficiency: a genome-wide association study. Lancet 2010; 376:180-8; PMID: 20541252; DOI: 10.1016/S0140-6736(10)60588-0.
115. Signorello LB, Shi J, Cai Q, Zheng W, Williams SM, Long J, et al. Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. PLoS One 2011; 6:e28623; PMID: 22205958; DOI: 10.1371/journal.pone.0028623.
116. Cheng JB, Levine MA, Bell NH, Mangelsdorf DJ, Russell DW. Genetic evidence that the human CYP2R1 enzyme is a key vitamin D 25-hydroxylase. Proc Natl Acad Sci U S A 2004; 101:7711-5; PMID: 15128933; DOI: 10.1073/pnas.0402490101.
117. Levine M, Dang A, Ding C, Fischer P, Singh R, Thacher T. Tropical rickets in Nigeria: Mutation of the CYP2R1 gene encoding vitamin D 25-hydroxylase as a cause of vitamin D dependent rickets. Bone 2007; 40:S60-1; DOI: 10.1016/j.bone.2007.04.079.
118. Dong Q, Miller WL. Vitamin D 25-hydroxylase deficiency. Mol Genet Metab 2004; 83:197-8; PMID: 15464435; DOI: 10.1016/j.ymgme.2004.07.006.
119. Abdullah MA, Salhi HS, Bakry LA, Okamoto E, Abomelha AM, Stevens B, et al. Adolescent rickets in Saudi Arabia: a rich and sunny country. J Pediatr Endocrinol Metab 2002; 15:1017-25; PMID: 12199329; DOI: 10.1515/JPEM.2002.15.7.1017.
120. Al Mutair AN, Nasrat GH, Russell DW. Mutation of the CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency. J Clin Endocrinol Metab 2012; 97:E2022-5; PMID: 22855339; DOI: 10.1210/jc.2012-1340.
121. Holick MF. The vitamin D deficiency pandemic and consequences for nonskeletal health: mechanisms of action. Mol Aspects Med 2008; 29:361-8; PMID: 18801384; DOI: 10.1016/j.mam.2008.08.008.
122. Sempos C, Vesper H, Phinny K, Thienpont L, Coates P. VDSP. Is there a U- or J-shaped Association between 25-Hydroxyvitamin D and All-Cause Mortality?. Results from the US Nationally Representative NHANES, JCEM 2012; .
123. Olama SM, Senna MK, Elarman MM, Elhawary G. Serum vitamin D level and bone mineral density in premenopausal Egyptian women with fibromyalgia. Rheumatol Int 2013; 33:185-92; PMID: 22311432; DOI: 10.1007/s00296-012-2361-0.
124. El Husseiny NM, Fahmy HM, Mohamed WA, Amin HH. Relationship between vitamin D and IL-23, IL-17 and macrophage chemoattractant protein-1 as markers of fibrosis in hepatitis C virus Egyptians. World J Hepatol 2012; 4:242-7; PMID: 22993666; DOI: 10.4254/wjh.v4.i8.242.
125. Schaalan MF, Mohamed WA, Amin HH. Vitamin D deficiency: correlation to interleukin-17, interleukin-23 and PIIINP in hepatitis C virus genotype 4. World J Gastroenterol 2012; 18:3738-44; PMID: 22851868; DOI: 10.3748/wjg.v18.i28.3738.
126. Hamza RT, Awwad KS, Ali MK, Hamed AI. Reduced serum concentrations of 25-hydroxy vitamin D in Egyptian patients with systemic lupus erythematosus: relation to disease activity. Med Sci Monit 2011; 17:CR711-8; PMID: 22129903; DOI: 10.12659/MSM.882131.
127. Alsayed A, Gad A, Azab A. Serum 25-hydroxyvitamin D concentrations and metabolic syndrome in Egyptian men. J Med Sci 2007; 7:850-4; DOI: 10.3923/jms.2007.850.854.
128. Khalili H, Talasaz AH, Salarifar M. Serum vitamin D concentration status and its correlation with early biomarkers of remodeling following acute myocardial infarction. Clin Res Cardiol 2012; 101:321-7; PMID: 22159952; DOI: 10.1007/s00392-011-0394-0.
129. Hosseinpanah F, Yarjanli M, Sheikholeslami F, Heibatollahi M, Eskandary PS, Azizi F. Associations between vitamin D and cardiovascular outcomes; Tehran Lipid and Glucose Study. Atherosclerosis 2011; 218:238-42; PMID: 21676397; DOI: 10.1016/j.atherosclerosis.2011.05.016.
130. Bonakdar ZS, Jahanshahifar L, Jahanshahifar F, Gholamrezaei A. Vitamin D deficiency and its association with disease activity in new cases of systemic lupus erythematosus. Lupus 2011; 20:1155-60; PMID: 21680639; DOI: 10.1177/0961203311405703.
131. Heidari B, Shirvani JS, Firouzjahi A, Heidari P, Hajian-Tilaki KO. Association between nonspecific skeletal pain and vitamin D deficiency. Int J Rheum Dis 2010; 13:340-6; PMID: 21199469; DOI: 10.1111/j.1756-185X.2010.01561.x.
132. Garakyaraghi M, Kerdegari M, Siavash M. Calcium and vitamin D status in heart failure patients in Isfahan, Iran. Biol Trace Elem Res 2010; 135:67-73; PMID: 19690819; DOI: 10.1007/s12011-009-8492-9.
133. Bonakdaran S, Varasteh AR. Correlation between serum 25 hydroxy vitamin D3 and laboratory risk markers of cardiovascular diseases in type 2 diabetic patients. Saudi Med J 2009; 30:509-14; PMID: 19370277.
134. Omrani GR, Masoompour SM, Sadegholvaad A, Larijani B. Effect of menopause and renal function on vitamin D status in Iranian women. East Mediterr Health J 2006; 12:188-95; PMID: 17037237.
135. Saliba W, Lavi I, Rennert HS, Rennert G. Vitamin D status in primary hyperparathyroidism. Eur J Intern Med 2012; 23:88-92; PMID: 22153538; DOI: 10.1016/j.ejim.2011.07.008.
136. Amital H, Szekanecz Z, Szücs G, Dankó K, Nagy E, Csépány T, et al. Serum concentrations of 25-OH vitamin D in patients with systemic lupus erythematosus (SLE) are inversely related to disease activity: is it time to routinely supplement patients with SLE with vitamin D?. Ann Rheum Dis 2010; 69:1155-7; PMID: 20439290; DOI: 10.1136/ard.2009.120329.
137. Bener A, Alsaied A, Al-Ali M, Al-Kubaisi A, Basha B, Abraham A, et al. High prevalence of vitamin D deficiency in type 1 diabetes mellitus and healthy children. Acta Diabetol 2009; 46:183-9; PMID: 18846317; DOI: 10.1007/s00592-008-0071-6.
138. Bin-Abbas BS, Jabari MA, Issa SD, Al-Fares AH, Al-Muhsen S. Vitamin D levels in Saudi children with type 1 diabetes. Saudi Med J 2011; 32:589-92; PMID: 21666940.
139. Al-Daghri NM, Al-Attas OS, Al-Okail MS, Alkharfy KM, Al-Yousef MA, Nadhrah HM, et al. Severe hypovitaminosis D is widespread and more common in non-diabetics than diabetics in Saudi adults. Saudi Med J 2010; 31:775-80; PMID: 20635011.
140. Banajeh SM. Nutritional rickets and vitamin D deficiency--association with the outcomes of childhood very severe pneumonia: a prospective cohort study. Pediatr Pulmonol 2009; 44:1207-15; PMID: 19911367; DOI: 10.1002/ppul.21121.
141. Shakinba M, Tefagh S, Nafei Z. The optimal dose of vitamin D in growing girls during academic years: a randomized trial. Turk J Med Sci 2011; 41:33-7.
142. Ghazi AA, Hosseinpanah F, M Ardakani E, Ghazi S, Hedayati M, Azizi F. Effects of different doses of oral cholecalciferol on serum 25(OH)D, PTH, calcium and bone markers during fall and winter in schoolchildren. Eur J Clin Nutr 2010; 64:1415-22; PMID: 20823895; DOI: 10.1038/ejcn.2010.169.
143. Gotsman I, Shauer A, Zwas DR, Hellman Y, Keren A, Lotan C, et al. Vitamin D deficiency is a predictor of reduced survival in patients with heart failure; vitamin D supplementation improves outcome. Eur J Heart Fail 2012; 14:357-66; PMID: 22308011; DOI: 10.1093/eurjhf/hfr175.
144. Soliman AT, Adel A, Wagdy M, Alali M, Aziz Bedair EM. Manifestations of severe vitamin D deficiency in adolescents: effects of intramuscular injection of a megadose of cholecalciferol. J Trop Pediatr 2011; 57:303-6; PMID: 20427425; DOI: 10.1093/tropej/fmq028.
145. Al-Daghri NM, Alkharfy KM, Al-Saleh Y, Al-Attas OS, Alokail MS, Al-Othman A, et al. Modest reversal of metabolic syndrome manifestations with vitamin D status correction: a 12-month prospective study. Metabolism 2012; 61:661-6; PMID: 22075268; DOI: 10.1016/j.metabol.2011.09.017.
146. Rajah J, Abdel-Wareth L, Haq A. Failure of alphacalcidol (1alpha-hydroxyvitamin D3) in treating nutritional rickets and the biochemical response to ergocalciferol. J Steroid Biochem Mol Biol 2010; 121:273-6; PMID: 20398760; DOI: 10.1016/j.jsbmb.2010.03.075.
147. Saadi HF, Dawodu A, Afandi BO, Zayed R, Benedict S, Nagelkerke N. Efficacy of daily and monthly high-dose calciferol in vitamin D-deficient nulliparous and lactating women. Am J Clin Nutr 2007; 85:1565-71; PMID: 17556694.
148. Rajah J, Jubeh JA, Haq A, Shalash A, Parsons H. Nutritional rickets and z scores for height in the United Arab Emirates: to D or not to D?. Pediatr Int 2008; 50:424-8; PMID: 18937749; DOI: 10.1111/j.1442-200X.2008.02700.x.
149. Saadi HF, Dawodu A, Afandi B, Zayed R, Benedict S, Nagelkerke N, et al. Effect of combined maternal and infant vitamin D supplementation on vitamin D status of exclusively breastfed infants. Matern Child Nutr 2009; 5:25-32; PMID: 19161542; DOI: 10.1111/j.1740-8709.2008.00145.x.
150. Porhashem Z, Biani M, Noreddini H, Bijani A, Hosseini S. Prevalence of osteoporosis and its association with serum vitamin D level in older people in Amirkola, North of Iran. Caspian J Intern Med 2012; 3:347-53.
151. Arabi A, Mahfoud Z, Zahed L, El-Onsi L, El-Hajj Fuleihan G. Effect of age, gender and calciotropic hormones on the relationship between vitamin D receptor gene polymorphisms and bone mineral density. Eur J Clin Nutr 2010; 64:383-91; PMID: 20145667; DOI: 10.1038/ejcn.2010.5.
152. El-Hajj Fuleihan G. Can the sunshine vitamin melt the fat?. Metabolism 2012; 61:603-10; PMID: 22304833; DOI: 10.1016/j.metabol.2011.12.006.
153. Fahed AC, El-Hage-Sleiman AK, Farhat TI, Nemer GM. Diet, genetics, and disease: a focus on the middle East and north Africa region. J Nutr Metab 2012; 2012:109037; PMID: 22536488; DOI: 10.1155/2012/109037.
154. Mehio Sibai A, Nasreddine L, Mokdad AH, Adra N, Tabet M, Hwalla N. Nutrition transition and cardiovascular disease risk factors in Middle East and North Africa countries: reviewing the evidence. Ann Nutr Metab 2010; 57:193-203; PMID: 21088386; DOI: 10.1159/000321527.
155. Shaygannejad V, Golabchi K, Haghighi S, Dehghan H, Moshayedi A. A Comparative Study of 25 (OH) Vitamin D Serum Levels in Patients with Multiple Sclerosis and Control Group in Isfahan, Iran. Int J Prev Med 2010; 1:195-201; PMID: 21566791.
156. Lerner A, Shapira Y, Agmon-Levin N, Pacht A, Ben-Ami Shor D, López HM, et al. The clinical significance of 25OH-Vitamin D status in celiac disease. Clin Rev Allergy Immunol 2012; 42:322-30; PMID: 21210250; DOI: 10.1007/s12016-010-8237-8.
157. Lerch C, Meissner T. Interventions for the prevention of nutritional rickets in term born children. Cochrane Database Syst Rev 2007; :CD006164; PMID: 17943890.
158. Cesur Y, Caksen H, Gündem A, Kirimi E, Odabaş D. Comparison of low and high dose of vitamin D treatment in nutritional vitamin D deficiency rickets. J Pediatr Endocrinol Metab 2003; 16:1105-9; PMID: 14594170; DOI: 10.1515/JPEM.2003.16.8.1105.
159. Winzenberg T, Powell S, Shaw KA, Jones G. Effects of vitamin D supplementation on bone density in healthy children: systematic review and meta-analysis. BMJ 2011; 342:c7254; PMID: 21266418; DOI: 10.1136/bmj.c7254.
160. Arabi A, Zahed L, Mahfoud Z, El-Onsi L, Nabulsi M, Maalouf J, et al. Vitamin D receptor gene polymorphisms modulate the skeletal response to vitamin D supplementation in healthy girls. Bone 2009; 45:1091-7; PMID: 19647104; DOI: 10.1016/j.bone.2009.07.074.
161. Kumar GT, Sachdev HS, Chellani H, Rehman AM, Singh V, Arora H, et al. Effect of weekly vitamin D supplements on mortality, morbidity, and growth of low birthweight term infants in India up to age 6 months: randomised controlled trial. BMJ 2011; 342:d2975; PMID: 21628364; DOI: 10.1136/bmj.d2975.
162. Hollis BW, Johnson D, Hulsey TC, Ebeling M, Wagner CL. Vitamin D supplementation during pregnancy: double-blind, randomized clinical trial of safety and effectiveness. J Bone Miner Res 2011; 26:2341-57; PMID: 21706518; DOI: 10.1002/jbmr.463.
163. Harvey NC, Javaid K, Bishop N, Kennedy S, Papageorghiou AT, Fraser R, et al. MAVIDOS Maternal Vitamin D Osteoporosis Study: study protocol for a randomized controlled trial. Trials 2012; 13:13; PMID: 22314083; DOI: 10.1186/1745-6215-13-13.
164. Martineau AR, Nhamoyebonde S, Oni T, Rangaka MX, Marais S, Bangani N, et al. Reciprocal seasonal variation in vitamin D status and tuberculosis notifications in Cape Town, South Africa. Proc Natl Acad Sci U S A 2011; 108:19013-7; PMID: 22025704; DOI: 10.1073/pnas.1111825108.
165. Martineau AR, Timms PM, Bothamley GH, Hanifa Y, Islam K, Claxton AP, et al. High-dose vitamin D(3) during intensive-phase antimicrobial treatment of pulmonary tuberculosis: a double-blind randomised controlled trial. Lancet 2011; 377:242-50; PMID: 21215445; DOI: 10.1016/S0140-6736(10)61889-2.
166. Coussens AK, Wilkinson RJ, Hanifa Y, Nikolayevskyy V, Elkington PT, Islam K, et al. Vitamin D accelerates resolution of inflammatory responses during tuberculosis treatment. Proc Natl Acad Sci U S A 2012; 109:15449-54; PMID: 22949664; DOI: 10.1073/pnas.1200072109.

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Vitamin D deficiency in Middle East and North Africa - June 2013

Hypovitaminosis D in the Middle East and North Africa: Prevalence, risk factors and impact on outcomes

XML File

Authors: Darina Bassil, Maya Rahme, Maha Hoteit and Ghada El-Hajj Fuleihan

Full Text

Introduction

Methods

Magnitude of the Problem and Predictors of Low Vitamin D Status

Is There a Genetic Basis for Low Vitamin D Levels and Rickets in the MENA?

Impact of Vitamin D on Surrogate Markers or Major Health Outcomes in MENA

Intervention Studies

Conclusion

Disclosure of Potential Conflicts of Interest

Acknowledgments

References

See also VitaminDWiki

Wikipedia Nov 2013

Attached files

Health Problems and D

Vitamin D deficiency in Middle East and North Africa - June 2013

Hypovitaminosis D in the Middle East and North Africa: Prevalence, risk factors and impact on outcomes

XML File

Authors: Darina Bassil, Maya Rahme, Maha Hoteit and Ghada El-Hajj Fuleihan

Full Text

Introduction

Methods

Magnitude of the Problem and Predictors of Low Vitamin D Status

Is There a Genetic Basis for Low Vitamin D Levels and Rickets in the MENA?

Impact of Vitamin D on Surrogate Markers or Major Health Outcomes in MENA

Intervention Studies

Conclusion

Disclosure of Potential Conflicts of Interest

Acknowledgments

References

See also VitaminDWiki

Wikipedia Nov 2013

Backlinks

Page actions

Attached files

Health Problems and D