Vitamin D Loading dose - 20,000 IU daily is not enough if obese, etc. (Cancer) great table and chart

Appropriate vitamin D loading regimen for patients with advanced lung cancer.

Nutr J. 2016 Oct 6;15(1):84.

Hoffer LJ1, Robitaille L2, Swinton N3, Agulnik J2,3, Cohen V2,3, Small D2,3, Pepe C2,3, Eintracht S4.

  • 1Lady Davis Institute for Medical Research, McGill University and Jewish General Hospital, 3755 Cote Sainte Catherine, Montreal, QC H3T 1E2, Canada. l.hoffer@mcgill.ca.

  • 2Lady Davis Institute for Medical Research, McGill University and Jewish General Hospital, 3755 Cote Sainte Catherine, Montreal, QC H3T 1E2, Canada.

  • 3Pulmonary Oncology Peter Brojde Lung Cancer Centre, Jewish General Hospital, Montreal, Canada.

  • 4Department of Diagnostic Medicine, Jewish General Hospital, Montreal, Canada.

20,000 IU for 14 days, followed by 10,000 IU Yet again we see that a fixed dose dose not help about half ot the people See also VitaminDWiki * Lung Cancer less likely if vitamin D (higher level or supplement) – meta-analysis May 2015 * Lung Cancer risk decreases 5 percent for every 2.5 nanogram increase in Vitamin D – meta-analysis Sept 2015 * A good level of vitamin D years earlier would have PREVENTED the Lung Cancer * Overview Lung cancer and vitamin D * Rapid Normalization of Vitamin D in Critically Ill Children (10,000 IU per kg) – clinical trial * Some studies have learned to vary the dose size with weight * Overview Loading of vitamin D * 18 fewer hospital days if given 500,000 IU of vitamin D while ventilated in ICU – RCT June 2016 * Loading Dose given over a span of 5 days * Chemotherapy and vitamin D - many studies * High levels of vitamin D increase the impact of Chemotherapy on the body * Which is great if the Chemo dose in lowered when Vitamin D is increased * If Chemo is not decreased an increased level of Vitamin D could prove to be deadly * Obese need 2X to 3X more vitamin D - Nov 2014 has the following chart image __Normal weight       Obese       (50 ng = 125)__

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Vitamin D response

image

Table 4 - Other Loading Dose studies

Table 4 Early time-point effects of oral vitamin D loading on plasma 25(OH)D concentrations of adults

First author, year

Number

Study population

BMI

Intervention

Time point

Mean 25(OH)D

Range or SD

[reference]

concentration

Weisman et al., 1986 [60]

13

Elderly

n.a.

100,000 IU in one dose

Baseline

29

14 days

88

SD 14

Ilahi et al., 2008 [54]

30

Healthy volunteers

27

100,00 IU in one dose

Baseline

27

7-21 daysa

105

SD 20

Romagnoli, 2008 [56]

8

Elderly nursing home

n.a.

300,000 IU in one dose

Baseline

33

3 days

120

n.a

7 days

128

30 days

152

Martineau et al., 2009 [55]

56

Normalvolunteers

n.a.

100,000 IU vitamin D2 in one

Baseline

34b

dose

7 days

102

50-140

11

Active tuberculosis

n.a.

100,000 IU vitamin D2 in one

Baseline

23b

dose

7 days

133

70-250

Cipriani et al., 2010 [61]

48

Healthy volunteers

24

600,000 IU in one dose

Baseline

35

3 days

193

SD ~68

15 days

193

30 days

155

Amrein et al., 2011 57

12

Critically ill

29

540,000 IU in one dose

Baseline

35

3 days

88

n.a.

7 days

96

Rossini et al., 2012 [58]

13

Elderly

29

100,000 IU in one dose

Baseline

66

7 days

85

SD ~20

14 days

83

30 days

84

12

29

300,000 IU in one dose

Baseline

64

7 days

96

SD ~20

14 days

95

30 days

86

12

29

600,000 IU in one dose

Baseline

54

7 days

156

SD ~30

14 days

152

30 days

129

Grossmann et al., 2012 59

15

Adults with cystic fibrosis

18.5

250,000 IU in one dose

Baseline

76

and acute illness

7 days

145

SD 34

Roth et al., 2012 [62]

34

Non-pregnant women

n.a.

70,000 IU in one dose

Baseline

54

7 days

79

~45-125

14 days

75

~40-140

27

Pregnant women

n.a.

70,000 IU in one dose

Baseline

39

7 days

67

~45-100

14 days

71

~50-120

De Jong et al., 2013 63

14

Elderly acute hip fracture

n.a.

150,000 IU as 50,000 IU/day

Baseline

30

for 3 days

7 days

81

47-108

54

n.a.

350,000 IU as 50,000 IU/day

Baseline

31

for 7 days

7 days

131

86-243

Table 4 Early time-point effects of oral vitamin D loading on plasma 25(OH)D concentrations of adults (Continued)

Drincic et al., 2013 [64]

20

Obese

38

10,000 IU per day

Baseline

58

7 days

80

n.a.

21 days

106

Cantor, 2014 [65]

18

Internal medicine

n.a

356,000 IU as 300,00 IU

Baseline

22

patients

followed by 4000 IU/day

14 days

102

50-202

32

n.a.

206,000 IU as150,000 IU

Baseline

55

followed by 4000 IU/day

14 days

108

58-185

Kearns et al., 2015 [66]

14

Healthy volunteers

24

250,000 IU in one dose

Baseline

41

5 days

102

70-149

Oliveri et al., 2015 [67]

11

Healthy volunteers

22

100,000 IU in one dose

Baseline

41

SD 12

7 days

105

11

21

100,000 IU vitamin D2 in one

Baseline

41

SD 28

dose

7 days

92

Rousseau et al., 2015 [68]

29

Healthy volunteers

n.a.

100,000 IU in one dose

Baseline

54

7 days

100

64-167

20

Acute burn injury

n.a.

100,000 IU in one dose

Baseline

18

7 days

48

12-84

Tukvadze et al., 2015 [69]

100

Active tuberculosis

n.a.

50,000 IU three times weekly

Baseline

35

14 days

175

n.a.

28 days

225

Present study

80

Lung cancer

26

20,000 IU/day for 14 days

Baseline

48

then 10,000 IU/day

14 days

106

16-238

21 days

116

15-258

BM! body mass index (kg/m2). 25(OH)D concentrations are expressed in nmol/L

aThe concentration peaked on day 7 and remained approximately constant throughout day 21

b Sum of 25(OH)D2 and 25(OH)D3


BACKGROUND:

Most patients attending cancer clinics have hypovitaminosis D. Correcting or preventing this abnormal condition could mitigate the emotional and physical complications of their disease, but clinical trials of vitamin D therapy in this setting are hindered by the unavailability of safe, effective and practical loading dose regimens.

METHODS:

In this single arm open-label pharmacokinetic trial, outpatients with advanced lung cancer consumed 20,000 IU vitamin D daily with the largest meal of the day for 14 days followed by 10,000 IU per day for a further 7 days . Plasma concentrations of 25-hydroxyvitamin D [25(OH)D], parathyroid hormone, calcium, vitamin C and C-reactive protein were measured on protocol days 0, 14 and 21, and serum vitamin D binding protein (VDBP) concentrations on days 0 and 21. As a secondary objective, preliminary information was obtained regarding clinical effects of rapid vitamin D loading on mood and symptoms by administering appropriate questionnaires two times at baseline and after 14 and 21 days of vitamin D therapy.

RESULTS:

Of the 91 patients enrolled in the study, 85 % had hypovitaminosis D and 41 % had hypovitaminosis C. Plasma VDBP concentrations were in the normal range. The vitamin D load increased the average plasma 25(OH)D concentration to 116?\ ± 34 nmol/L (mean ± SD); the median concentration was 122 nmol/L (interquartile range 103-134); VDBP concentrations did not change. Final plasma 25(OH)D concentrations were subnormal (<75 nmol/L) for 13 % of the patients and sub-target (<120 nmol/L) for 44 % of them. In most cases, subnormal and sub-target 25(OH)D concentrations were attributable to obesity and/or a low baseline 25(OH)D concentration. Mood and symptom scores did not change significantly throughout the 3-week protocol.

CONCLUSION:

Hypovitaminosis D and C are very common in outpatients with advanced lung cancer. A vitamin D load of 20,000 IU per day for 14 days failed to achieve the target concentration in 44 % of the participants in this tria l. These results suggest that a loading dose of 30,000 IU per day for 14 days would be safe and effective for patients who are obese or at risk of severe hypovitaminosis D . The preliminary nature of the study design, and the failure to achieve target 25(OH)D concentrations for a large proportion of the patients, do not allow any firm conclusion about the clinical effects of correcting hypovitaminosis D in this patient population. Nevertheless, no evidence was obtained that partial correction of hypovitaminosis D greatly improved mood, reduced distress or relieved cancer-related symptoms.

This trial was registered at clinicaltrials.gov as NCT01631526.

PMID: 27716304 DOI: 10.1186/s12937-016-0203-8