French pediatric consensus: 30 – 60 ng of Vitamin D – Feb 2022

Note by VitaminDWiki: The formatting of the PDF made it difficult to extract the data.
The following is just a small portion of the PDF

Vitamin D and calcium intakes in general pédiatrie populations: A French expert consensus paper

Arch Pediatr. 2022 Mar 16;S0929-693X(22)00073-2. doi: 10.1016/j.arcped.2022.02.008.
J. Bacchettaa,b'c'*, T. Edouardd, G. Lavernye, J. Bernardorbf, A. Bertholet-Thomasa,b, M. Castanetg, C. Garniera, I. Gennerod, J. Harambath'', A. LapillonneJ',k, A. Molin1, C. Nauda, J.P. Sallesd,
S. Laboriem, P. Touniann, A. Linglarto

Objectives: Nutritional vitamin D supplements are often used in general pediatrics. Here, the aim is to address vitamin D supplementation and calcium nutritional intakes in newborns, infants, children, and adolescents to prevent vitamin D deficiency and rickets in general populations.

Study design: We formulated clinical questions relating to the following categories: the Patient (or Population) to whom the recommendation will apply; the Intervention being considered; the Comparison (which may be “no action,” placebo, or an alternative intervention); and the Outcomes affected by the intervention (PICO). These PICO elements were arranged into the questions to be addressed in the literature searches. Each PICO question then formed the basis for a statement. The population covered consisted of children aged between 0 and 18 years and premature babies hospitalized in neonatology. Two groups were assembled: a core working group and a voting panel from different scientific pediatric committees from the French Society of Pediatrics and national scientific societies.

Results: We present here 35 clinical practice points (CPPs) for the use of native vitamin D therapy (ergocalciferol, vitamin D2 and cholecalciferol, vitamin D3) and calcium nutritional intakes in general pediatric populations.

Conclusion: This consensus document was developed to provide guidance to health care professionals on the use of nutritional vitamin D and dietary modalities to achieve the recommended calcium intakes in general pediatric populations. These CPPs will be revised periodically. Research recommendations to study key vitamin D outcome measures in children are also suggested.
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Clinical practice points
  • 1. We recommend measuring only serum total 25(OH)D concentration in assessing vitD status in children.
  • 2. We recommend measuring serum total 25(OH)D concentration in the same lab for a given child.
  • 3. We recommend that assays of 1,25(OH)2D or other metabolites should not be used routinely in pediatrics.
  • 4. We do not recommend systematic measurement of serum total 25(OH)D concentration in general pediatric populations.
  • 5. We recommend measurement of serum total 25(OH)D levels when there are symptoms of rickets.
  • 6. We recommend a 25(OH)D level >20 ng/mL (50 nmol/L) in general pediatric populations to prevent rickets.
  • 7. We suggest a 25(OH)D level >30 ng/mL (75 nmol/L) in general pediatric populations to avoid any mineralization defects and seasonal variability.
  • 8. We suggest a 25(OH)D level <60 ng/mL (150 nmol/L) in general pediatric populations.
  • 9. Toxicity has been described when 25(OH)D levels are above 80 ng/mL (200 nmol/L) in general pediatric populations.
  • 10. We recommend supplementing healthy children 0-18 years of age with a minimum of 400 1U of vitD per day. Level A evidence
  • 11. We recommend supplementing healthy children 0-18 years of age with a maximum of 800 1U of vitD per day. Level C evidence
  • 12. We recommend daily supplementation in children 0-2 years using D2 or D3.
  • 13. We suggest preferring daily supplementation in children 2 -18 years using D2 or D3.
  • 14. We suggest intermittent supplementation in the case of nonadherence in children 2-18 years using vitD3 with either 50,000 1U quarterly or 80,000-100,000 1U twice in fall and winter.
  • 15. We recommend avoiding of 200,000 1U of vitD in one shot.
  • 16. We recommend using only licensed pharmaceutical native vitD supplements.
  • 17. We recommend a minimum of 800 1U and a maximum of 1600 1U of vitD per day in children 2-18 years of age in the case of decreased availability of vitD (obesity, black ethnicity, absence of skin exposure to sun) or decreased intake (vegan diet).
  • 18. In such children, we recommend daily supplementation with vitD2 or D3.
  • 19. In such children, we suggest intermittent supplementation in the case of nonadherence using vitD3 with either 50,000 1U every 6 weeks or 80,000-100,000 1U quarterly.
  • 20. We recommend considering at increased risk of developing rickets and vitD deficiency children and teenagers with the following conditions: malabsorption, maldigestion, chronic kidney disease, nephrotic syndrome, cholestasis, hepatic insufficiency, cystic fibrosis, secondary bone fragility, chronic inflammatory diseases, anorexia nervosa, skin diseases, anticonvulsant medications, or long-term corticosteroids.
  • 21. We suggest that general pediatricians/physicians verify adherence to vitD supplementation in these children.
  • 22. We recommend that physicians rule out the use of over-the-counter vitD preparations before prescribing native vitD supplementation.
  • 23. We suggest monitoring 25(OH)D levels in patients receiving treatment doses above the upper ranges currently recommended.
  • 24. We recommend measuring 25(OH)D levels in the following conditions to adjust vitD supplementation: family history of vitD intoxication, hypercalcemia, hypercalciuria, kidney stones, and/or nephrocalcinosis.
  • 25. We suggest preferring daily vitD supplementation in these patients.
  • 26. We recommend that, from the age of 1 to 18 years, children and adolescents should consume at least three to four portions of dairy products per day to cover calcium needs.
  • 27. We recommend prescribing 500-1000 mg per day of calcium supplementation in children and adolescents receiving less than 300 mg adjusted for calcium bioavailability of nutritional calcium per day, especially in those following a vegan diet.
    - - - - Nutritional calcium
  • 28. We recommend evaluating dietary calcium intakes in children with fractures and bone pain.
  • 29. Diagnosis of calcium deficiency requires a dietary calcium intake evaluation, radiographs of wrists and knees, and measurement of plasma ALP, PTH, 25(OH)D, calcium and phosphate, and urinary excretion of calcium.
    - - - -PREMATURE
  • 30 We recommend optimizing nutritional calcium and phosphate intakes in premature neonates
  • 31 We suggest that, during the initial stay in the NICU, preterm infants receive between 600 IU and 1000 IU per day of vitD, taking into account the content of vitD in milk and parenteral nutrition, vitD supplementation during pregnancy, and birth weight
  • 32 We recommend measurement of 25(OH)D in children born before 32 weeks of gestation or weighing less than 1500 grams at 1 month of age
  • 33 We recommend 50 nmol/L as the lower target level and 120 nmol/L as the upper target level of 25 (OH)D in premature neonates
  • 34. After discharge from the NICU, we suggest following recommendations in general pediatric populations.
    - - - - French overseas territories:
  • 35. We suggest the same pattern of supplementation as in Metropolitan France.

VitaminDWiki observations on consensus
  • Consensus 9 says levels >80 = toxicity. Do not recall seeing that in any pediatric or adult studies
  • Consensus 10 and 11 incorrectly recommend the same amount independent of age
    • See green chart below
  • Consensus 12, 13, 18 says D2 is OK - but vets declared 10 years ago that no mammal should ever be given D2
  • Consensus 14, 19 says quarterly and twice a year supplementation is OK - It is not
  • Consensus 147 says up to 1600 IU in special conditions. AMA years ago recommended 1600 IU normally
  • Consensus 33 says max 48 ng for preemies but says max 60 ng in #8
  • Consensus fails to comment on injections being useful for infrequent supplementation
  • Consensus fails to comment on getting vitamin D via breastfeeding
  • Consensus fails to comment on gut-friendly forms of vitamin D needed sometimes
  • Consensus fails to comment on the use of loading dose to quickly raise vitamin D levels

Open Questions

- What are the molecular and cellular mechanisms underlying 1,25D3-dependent calcium homeostasis?
- Are extraskeletal effects observed in adults also applicable in children?
- Is CYP27B1 regulated in the same way in children as in adults in all the target cells?
- What other metabolites of vitD are interesting to evaluate?
- Are adult data adaptable to children?
- How should data be adapted from RCTs conducted in vitD-deficient subjects in general pediatric populations?
- Could the weekly supplementation be used in general pediatric populations?
- What are the real-life data (insurance database)?
- What would be the ideal vitD supplementation protocol in obese children, depending on their ethnicity?
- How should data be adapted from RCTs conducted in vitD-deficient subjects in general pediatric populations?
- What is the optimal schedule of vitD supplementation and monitoring in children and teenagers with hypercalciuria and nephrolithiasis?
- How should the variability of calcium absorption be evaluated in children?
- Is there a reliable laboratory parameter to assess calcium status and to recommend calcium supplementation in the case of deficiency?
- What is the role of C3 epimerization in neonates and pregnant women?
- What is the optimal schedule of vitD supplementation and monitoring in premature babies?
- What is the ideal upper target of 25(OH)D levels in premature babies for bone outcomes but also global outcomes?
- What is the exact frequency of vitD deficiency and overdose in very preterm infants?
- Establish data on vitD status and needs for supplementation in overseas territories


References

  • 1 Adams JS, Hewison M. Update in vitamin D. J Clin Endocrinol Metab 2010;95:471-8.
  • 2 Holick MF. High prevalence of vitamin D inadequacy and implications for health. Mayo Clin Proc 2006;81:353-73.
  • 3 Vidailhet M, Mallet E, Bocquet A, et al. Vitamin D: still a topical matter in children and adolescents. A position paper by the Committee on Nutrition of the French Society ofPaediatrics. Arch Pediatr2012;19:316-28.
  • 4 Braegger C, Campoy C, Colomb V, et al. Vitamin D in the healthy European paediatric population.JPediatr Gastroenterol Nutr 2013;56:692-701.
  • 5 American Academy of Pediatrics Steering Committee on Quality Improvement and Management. Classifying recommendations for clinical practice guidelines. Pediatrics 2004;114:874-7.
  • 6 Armas LAG, Hollis BW, Heaney RP. Vitamin D2 is much less effective than vitamin D3 in humans. J Clin Endocrinol Metab 2004;89:5387-91.
  • 7 Holick MF. Vitamin D status: measurement, interpretation, and clinical application. Ann Epidemiol 2009;19:73-8.
  • 8 Huet T, Laverny G, Ciesielski F, et al. A vitamin D receptor selectively activated by gemini analogs reveals ligand dependent and independent effects. Cell Rep 2015;10:516-26.
  • 9 Lee SM, Goellner JJ, O'Brien CA, et al. A humanized mouse model of hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia. Endocrinology 2014;155:4137-48.
  • 10 Rochel N, Molnar F. Structural aspects of Vitamin D endocrinology. Mol Cell Endocrinol 2017;453:22-35.
  • 11 Neme A, Seuter S, Malinen M, et al. In vivo transcriptome changes of human white blood cells in response to vitamin D. J Steroid Biochem Mol Biol 2019;188:71-6.
  • 12 Bjerg LN, Halgreen JR, Hansen SH, et al. An evaluation of total 25-hydroxyvita-min D assay standardization: where are we today? J Steroid Biochem Mol Biol 2019;190:224-33.
  • 13 Lensmeyer G, Poquette M, Wiebe D, et al. The C-3 epimer of 25-hydroxyvitamin D(3)is present in adultserum.JClin Endocrinol Metab 2012;97:163-8.
  • 14 Tapan S, Sertoglu E, Uyanik M. Importance of C-3 epimer of 25-hydroxyvitamin D in dried blood spots of neonatal population. IntJ Cancer 2015;137:750.
  • 15 Hollis BW. Assessment and interpretation of circulating 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D in the clinical environment. Endocrinol Metab Clin N Am 2010;39:271-86 table ofcontents.
  • 16 Holick MF, Binkley NC, Bischoff-Ferrari HA, et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine society clinical practice guideline. J Clin Endocrinol Metab 2011;96:1911-30.
  • 17 Sattar N, Welsh P, Panarelli M, et al. Increasing requests for vitamin D measurement: costly, confusing, and without credibility. Lancet Lond Engl 2012;379:95-
  • 6.
  • 18 MaguireJL, Birken C, Thorpe KE, et al. Parathyroid hormone as a functional indicator of vitamin D sufficiency in children. JAMA Pediatr 2014;168:383-5.
  • 19 Vierucci F, Del Pistoia M, Fanos M, et al. Vitamin D status and predictors ofhypo-vitaminosis D in Italian children and adolescents: a cross-sectional study. Eur J Pediatr 2013;172:1607-17.
  • 20 Atapattu N, Shaw N, Hogler W. Relationship between serum 25-hydroxyvitamin D and parathyroid hormone in the search for a biochemical definition ofvitamin D deficiency in children. Pediatr Res 2013;74:552-6.
  • 21 Wagner CL, Greer FR, American Academy ofPediatrics Section on Breastfeeding. American Academy of Pediatrics Committee on Nutrition. Prevention of rickets and vitamin D deficiency in infants, children, and adolescents. Pediatrics 2008;122:1142-52.
  • 22 Misra M, Pacaud D, PetrykA,et al. Vitamin D deficiency in children and its management: review of current knowledge and recommendations. Pediatrics 2008;122:398-417.
  • 23 Priemel M, von Domarus C, Klatte TO, 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.
  • 24 Durup D, Jorgensen HL, Christensen J, et al. A reverse J-shaped association between serum 25-hydroxyvitamin D and cardiovascular disease mortality: the CopD study.JClin Endocrinol Metab 2015;100:2339-46.
  • 25 Sempos CT, Durazo-Arvizu RA, Dawson-Hughes B, et al. Is there a reverse J-shaped association between 25-hydroxyvitamin D and all-cause mortality? Results from the U.S. nationally representative NHANES. J Clin Endocrinol Metab 2013;98:3001-9.
  • 26 Araki T, Holick MF, Alfonso BD, et al. Vitamin D intoxication with severe hypercalcemia due to manufacturing and labeling errors of two dietary supplements made in the United States. J Clin Endocrinol Metab 2011;96:3603-8.
  • 27 Hamo S, Freychet C, Bertholet-Thomas A, et al. Vitamin D supplementation: not too much, not too little!. Arch Pédiatr 2015;22:868-71.
  • 28 Vitamin D supplementation: recommendations for Canadian mothers and infants. Paediatr Child Health 2007;12:583-98.
  • 29 Allen KJ, Panjari M, Koplin JJ, et al. VITALITY trial: protocol for a randomised controlled trial to establish the role of postnatal vitamin D supplementation in infant immune health. BMJ Open 2015;5:e009377.
  • 30 Dawodu A, Davidson B, Woo Jg, et al. Sun exposure and vitamin D supplementation in relation to vitamin D status of breastfeeding mothers and infants in the global exploration of human milk study. Nutrients 2015;7:1081-93.
  • 31 Kramer CK, Ye C, Swaminathan B, et al. The persistence of maternal vitamin D deficiency and insufficiency during pregnancy and lactation irrespective of season and supplementation. Clin Endocrinol 2016;84:680-6 (Oxf).
  • 32 Abrams SA. Vitamin D in preterm and full-term infants. Ann Nutr Metab 2020;76 (Suppl 2):6-14.
  • 33 Gordon CM, Feldman HA, Sinclair L, et al. Prevalence of vitamin D deficiency among healthy infants and toddlers. Arch Pediatr Adolesc Med 2008;162:505-12.
  • 34 Gallo S, Hazell T, Vanstone CA, et al. Vitamin D supplementation in breastfed infants from Montreéal, Canada: 25-hydroxyvitamin D and bone health effects from a follow-up study at 3 years of age. Osteoporos Int 2016;27:2459-66.
  • 35 Rosendahl J, Valkama S, Holmlund-Suila E, et al. Effect of higher vs standard dosage of vitamin D3 supplementation on bone strength and infection in healthy infants: a randomized clinical trial. JAMA Pediatr 2018;172:646-54.
  • 36 Specker BL, Ho ML, Oestreich A, et al. Prospective study ofvitamin D supplementation and rickets in China. J Pediatr 1992;120:733-9.
  • 37 Bagnoli F, Casucci M, Toti S, et al. Is vitamin D supplementation necessary in healthy full-term breastfed infants? A follow-up study of bone mineralization in healthy full-term infants with and without supplemental vitamin D. Minerva Pediatr 2013;65:253-60.
  • 38 Savino F, Viola S, Tarasco V, et al. Bone mineral status in breast-fed infants: influence of vitamin D supplementation. Eur J Clin Nutr 2011;65:335-9.
  • 39 Lewis RD, Laing EM, Hill Gallant KM, et al. A randomized trial of vitamin D3 supplementation in children: dose-response effects on vitamin D metabolites and calcium absorption. J Clin Endocrinol Metab 2013;98:4816-25.
  • 40 Rajakumar K, Moore CG, Yabes J, et al. Estimations of dietary vitamin D requirements in black and white children. Pediatr Res 2016;80:14-20.
  • 41 Ferira AJ, Laing EM, Hausman DB, et al. Vitamin D supplementation does not impact insulin resistance in black and white children. J Clin Endocrinol Metab 2016;101:1710-8.
  • 42 Mortensen C, Damsgaard CT, Hauger H, et al. Estimation of the dietary requirement for vitamin D in white children aged 4-8 y: a randomized, controlled, dose-response trial. AmJ Clin Nutr 2016;104:1310-7.
  • 43 Aglipay M, Birken CS, Parkin PC, et al. Effect of high-dose vs standard-dose wintertime vitamin D supplementation on viral upper respiratory tract infections in young healthy children. JAMA 2017;318:245-54.
  • 44 Ohlund I, Lind T, Hernell O, et al. Increased vitamin D intake differentiated according to skin color is needed to meet requirements in young Swedish children during winter: a double-blind randomized clinical trial. Am J Clin Nutr 2017;106:105-12.
  • 45 Marwaha RK, Mithal A, Bhari N, et al. Supplementation with three different daily doses of vitamin D3 in healthy pre-pubertal school girls: a cluster randomized trial. Indian Pediatr 2018;55:951 -6.
  • 46 Hauger H, Molgaard C, Mortensen C, et al. Winter cholecalciferol supplementation at 55°N has no effect on markers of cardiometabolic risk in healthy children aged 4-8 years. J Nutr 2018;148:1261 -8.
  • 47 Hauger H, Ritz C, Mortensen C, et al. Winter cholecalciferol supplementation at 55°N has little effect on markers of innate immune defense in healthy children aged 4-8 years: a secondary analysis from a randomized controlled trial. Eur J Nutr 2019;58:1453-62.
  • 48 Mortensen C, Molgaard C, Hauger H, et al. Winter vitamin D3 supplementation does not increase muscle strength, but modulates the IGF-axis in young children. EurJ Nutr2019;58:1183-92.
  • 49 Ohlund I, Lind T, Hernell O, et al. Vitamin D status and cardiometabolic risk markers in young Swedish children: a double-blind randomized clinical trial comparing different doses of vitamin D supplements. Am J Clin Nutr 2020;111:779-86.
  • 50 Esterle L, Sabatier JP, Guillon-Metz F, et al. Milk, rather than other foods, is associated with vertebral bone mass and circulating IGF-1 in female adolescents. Osteoporos Int 2009;20:567-75.
  • 51 Winzenberg T, Powell S, Shaw KA, et al. Effects of vitamin D supplementation on bone density in healthy children: systematic review and meta-analysis. BMJ 2011;342:c7254.
  • 52 Dolinsky DH, Armstrong S, Mangarelli C, et al. The association between vitamin D and cardiometabolic risk factors in children: a systematic review. Clin Pediatr 2013;52:210-23 (Phila).
  • 53 Beveridge LA, Khan F, Struthers AD, et al. Effect of vitamin D supplementation on markers of vascular function: a systematic review and individual participant meta-analysis. J Am Heart Assoc 2018;7:e008273.
  • 54 Kord-Varkaneh H, Rinaldi G, Hekmatdoost A, et al. The influence of vitamin D supplementation on IGF-1 levels in humans: a systematic review and metaanalysis. Ageing Res Rev 2020;57:100996.
  • 55 Farrokhyar F, Sivakumar G, Savage K, et al. Effects of vitamin D supplementation on serum 25-hydroxyvitamin D concentrations and physical performance in athletes: a systematic review and meta-analysis of randomized controlled trials. Sports Med Auckl NZ 2017;47:2323-39.
  • 56 Iyengar A, Kamath N, Reddy HV, et al. Determining the optimal cholecalciferol dosing regimen in children with CKD: a randomized controlled trial. Nephrol Dial Transplant 2022;37:326-34.
  • 57 Simon AE, Ahrens KA. Adherence to vitamin D intake guidelines in the United States. Pediatrics 2020;145:e20193574.
  • 58 Flot C, Porquet-Bordes V, Bacchetta J, et al. Demographic characteristics, risk factors, and presenting features of children with symptomatic nutritional rickets: a french series. Horm Res Paediatr 2020;93:304-12.
  • 59 Cesur Y, Caksen H, Gündem A, et al. Comparison of low and high dose of vitamin D treatment in nutritional vitamin D deficiency rickets. J Pediatr Endocrinol Metab 2003;16:1105-9.
  • 60 Mittal H, Rai S, Shah D, et al. 300,000 IU or 600,000 IU of oral vitamin D3 for treatment of nutritional rickets: a randomized controlled trial. Indian Pediatr 2014;51:265-72.
  • 61 Vülimüki VV, Lüyttyniemi E, Pekkarinen T, et al. J. How well are the optimal serum 25OHD concentrations reached in high-dose intermittent vitamin D therapy? A placebo-controlled study on comparison between 100 000 IU and 200 000 IU of oral D3 every 3 months in elderly women. Clin Endocrinol 2016;84:837-44 (Oxf).
  • 62 ANSM. Internet. Vitamine D chez l'enfant: recourir aux medicaments et non aux compléments alimentaires pour prévenir le risque de surdosage. Publie le 27 janvier 2021 - Mis a jour le 17 mars 2021. https://www.ansm.sante.fr/S-informer/Points-d-information-Points-d-information/Vitamine-d-chez-l-enfant-recourir-aux-medicaments-et-non-aux-complements-alimentaires-pour-prevenir-le-risque-de-surdosage.
  • 63 Taylor PN, Davies JS. A review of the growing risk of vitamin D toxicity from inappropriate practice. Br J Clin Pharmacol 2018;84:1121 -7.
  • 64 Dong Y, Stallmann-Jorgensen IS, Pollock NK, et al. A 16-week randomized clinical trial of 2000 international units daily vitamin D3 supplementation in black youth: 25-hydroxyvitamin D, adiposity, and arterial stiffness. J Clin Endocrinol Metab 2010;95:4584-91.
  • 65 Golzarand M, Hollis BW, Mirmiran P, et al. Vitamin D supplementation and body fat mass: a systematic review and meta-analysis. Eur J Clin Nutr 2018;72:1345-57.
  • 66 Kelishadi R, Salek S, Salek M, et al. Effects of vitamin D supplementation on insulin resistance and cardiometabolic risk factors in children with metabolic syndrome: a triple-masked controlled trial. J Pediatr 2014;90:28-34 (Rio J).
  • 67 Nader NS, Aguirre Castaneda R, Wallace J, et al. Effect ofvitamin D3 supplementation on serum 25(OH)D, lipids and markers of insulin resistance in obese adolescents: a prospective, randomized, placebo-controlled pilot trial. Horm Res Paediatr2014;82:107-12.
  • 68 Javed A, Vella A, Balagopal PB, et al. Cholecalciferol supplementation does not influence b-cell function and insulin action in obese adolescents: a prospective double-blind randomized trial. J Nutr 2015;145:284-90.
  • 69 Talib HJ, Ponnapakkam T, Gensure R, et al. Treatment of vitamin D deficiency in predominantly hispanic and black adolescents: a randomized clinical trial. J Pediatr 2016;170:266-72 .e1.
  • 70 Rajakumar K, Moore CG, Khalid AT, et al. Effect of vitamin D3 supplementation on vascular and metabolic health of vitamin D-deficient overweight and obese children: a randomized clinical trial. AmJ Clin Nutr 2020;111:757-68.
  • 71 Lemale J, Mas E, Jung C, et al. Vegan diet in children and adolescents. Recommendations from the French-speaking Pediatric Hepatology, Gastroenterology and Nutrition Group (GFHGNP). Arch Pediatr 2019;26:442-50.
  • 72 Parsons TJ, van Dusseldorp M, van der Vliet M, et al. Reduced bone mass in Dutch adolescents fed a macrobiotic diet in early life. J Bone Miner Res 1997;12:1486-94.
  • 73 Grüber U, Kisters K. Influence of drugs on vitamin D and calcium metabolism. Dermatoendocrinol 2012;4:158-66.
  • 74 Edouard T, Guillaume-Czitrom S, Bacchetta J, et al. Guidelines for the management of children at risk of secondary bone fragility: expert opinion of a French working group. Arch Pediatr 2020;27:393-8.
  • 75 Shroff R, Wan M, Nagler EV, et al. Clinical practice recommendations for native vitamin D therapy in children with chronic kidney disease Stages 2-5 and on dialysis. Nephrol Dial Transplant 2017;32:1098-113.
  • 76 Smyth AR, Bell SC, Bojcin S, et al. European cystic fibrosis society standards of care: best practice guidelines. J CystFibros 2014;13(Suppl 1):S23-42.
  • 77 Marcinowska-Suchowierska E, Kupisz-Urbaéska M, Lukaszkiewicz J, et al. Vitamin D toxicity-a clinical perspective. Front Endocrinol 2018;9:550.
  • 78 Molin A, Baudoin R, Kaufmann M, et al. CYP24A1 mutations in a cohort of hyper-calcemic patients: evidence for a recessive trait. J Clin Endocrinol Metab 2015;100:E1343-52.
  • 79 Allen LH. Calcium bioavailability and absorption: a review. Am J Clin Nutr 1982;35:783-808.
  • 80 Kobayashi A, Kawai S, Obe Y, et al. Effects of dietary lactose and lactase preparation on the intestinal absorption of calcium and magnesium in normal infants. AmJ Clin Nutr 1975;28:681-3.
  • 81 Thacher TD, Aliu O, Griffin IJ, et al. Meals and dephytinization affect calcium and zinc absorption in Nigerian children with rickets. J Nutr 2009;139: 926-32.
  • 82 Weaver CM, Heaney RP, Martin BR, et al. Human calcium absorption from whole-wheat products. J Nutr 1991;121:1769-75.
  • 83 ANSES (Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail). Internet. Ciqual, French food composition table. https://ciq-ual.anses.fr/.
  • 84 European Food Safety Authority. Scientific Opinion on nutrient requirements and dietary intakes of infants and young children in the European Union. EFSA J 2013;11:3408.
  • 85 Thandrayen K, Pettifor JM. The roles of vitamin D and dietary calcium in nutritional rickets. Bone Rep 2018;8:81-9.
  • 86 Creo AL, Thacher TD, Pettifor JM, et al. Nutritional rickets around the world: an update. Paediatr Int Child Health 2017;37:84-98.
  • 87 Lieben L, Masuyama R, Torrekens S, et al. Normocalcemia is maintained in mice under conditions of calcium malabsorption by vitamin D-induced inhibition of bone mineralization.J Clin Invest2012;122:1803-15.
  • 88 Djennane M, Lebbah S, Roux C, et al. Vitamin D status of schoolchildren in Northern Algeria, seasonal variations and determinants of vitamin D deficiency. Osteoporos Int 2014;25:1493-502.
  • 89 Schnitzler CM, Pettifor JM. Calcium deficiency rickets in African adolescents: cortical bone histomorphometry. JBMR Plus 2019;3:e10169.
  • 90 Munns CF, Shaw N, Kiely M, et al. Global consensus recommendations on prevention and management of nutritional rickets. J Clin Endocrinol Metab 2016;101:394-415.
  • 91 Burris HH, Van Marter LJ, McElrath TF, et al. Vitamin D status among preterm and full-term infants at birth. Pediatr Res 2014;75:75-80.
  • 92 Kassai MS, Cafeo FR, Affonso-Kaufman FA, et al. Vitamin D plasma concentrations in pregnant women and their preterm newborns. BMC Pregnancy Childbirth 2018;18:412.
  • 93 Kim I, Kim SS, Song JI, et al. Association between vitamin D level at birth and respiratory morbidities in very-low-birth-weight infants. Korean J Pediatr 2019;62:166-72.
  • 94 Cetinkaya M, Cekmez F, Erener-Ercan T, et al. Maternal/neonatal vitamin D deficiency: a risk factor for bronchopulmonary dysplasia in preterms? J Perinatol 2015;35:813-7.
  • 95 Cetinkaya M, Erener-Ercan T, Kalayci-Oral T, et al. Maternal/neonatal vitamin D deficiency: a new risk factor for necrotizing enterocolitis in preterm infants? J Perinatol 2017;37:673-8.
  • 96 Natarajan CK, Sankar MJ, Agarwal R, et al. Trial of daily vitamin D supplementation in preterm infants. Pediatrics 2014;133:e628-34.
  • 97 Fort P, Salas AA, Nicola T, et al. A comparison of 3 vitamin D dosing regimens in extremely preterm infants: a randomized controlled trial. J Pediatr 2016;174: 132-8 .e1.
  • 98 Backstrom MC, Maki R, Kuusela AL, et al. Randomised controlled trial of vitamin D supplementation on bone density and biochemical indices in preterm infants. Arch Dis Child Fetal Neonatal Ed 1999;80:F161-6.
  • 99 Mathur NB, Saini A, Mishra TK. Assessment of adequacy of supplementation of vitamin D in very low birth weight preterm neonates: a randomized controlled trial. J Trop Pediatr2016;62:429-35.
  • 100 Alizadeh Taheri P, Sajjadian N, Beyrami B, et al. Prophylactic effect of low dose vitamin D in osteopenia of prematurity: a clinical trial study. Acta Med Iran 2014;52:671-4.
  • 101 Anderson-Berry A, Thoene M, Wagner J, et al. Randomized trial of two doses of vitamin D3 in preterm infants <32 weeks: dose impact on achieving desired serum 25(OH)D3 in a NICU population. PLoS One 2017;12:e0185950.
  • 102 Al-Beltagi M, Rowiesha M, Elmashad A, et al. Vitamin D status in preterm neonates and the effects of its supplementation on respiratory distress syndrome. Pediatr Pulmonol 2020;55:108-15.
  • 103 Bozkurt O, Uras N, Sari FN, et al. Multi-dose vitamin d supplementation in stable very preterm infants: prospective randomized trial response to three different vitamin D supplementation doses. Early Hum Dev 2017;112:54-9.
  • 104 Bae YJ, Kratzsch J. Vitamin D and calcium in the human breast milk. Best Pract Res Clin Endocrinol Metab 2018;32:39-45.
  • 105 Mitchell SM, Rogers SP, Hicks PD, et al. High frequencies of elevated alkaline phosphatase activity and rickets exist in extremely low birth weight infants despite current nutritional support. BMC Pediatr 2009;9:47.
  • 106 Viswanathan S, Khasawneh W, McNelis K, et al. Metabolic bone disease: a continued challenge in extremely low birth weight infants. JPEN J Parenter Enteral Nutr 2014;38:982-90.
  • 107 Mohamed M, Kamleh M, Muzzy J, et al. Association of protein and vitamin D intake with biochemical markers in premature osteopenic infants: a case-control study. Front Pediatr 2020;8:546544.
  • 108 Schulz EV, Wagner CL. History, epidemiology and prevalence of neonatal bone mineral metabolic disorders. Semin Fetal Neonatal Med 2020;25:101069.
  • 109 McCarthy RA, McKenna MJ, Oyefeso O, et al. Vitamin D nutritional status in preterm infants and response to supplementation. BrJ Nutr 2013;110:156-63.
  • 110 Tergestina M, Rebekah G, Job V, et al. A randomized double-blind controlled trial comparing two regimens of vitamin D supplementation in preterm neonates. J Perinatol 2016;36:763-7.
  • 111 Schell-Feith EA, Kist-van Holthe JE, van der Heijden AJ. Nephrocalcinosis in preterm neonates. Pediatr Nephrol 2010;25:221 -30 Berl Ger.
  • 112 KolodziejczykA, Borszewska-Kornacka MK, Seliga-SiweckaJ. Monitored supplementation of vitamin D in preterm infants (MOSVID trial): study protocol for a randomised controlled trial. Trials 2017;18:424.
  • 113 Vierge M, Laborie S, Bertholet-Thomas A, et al. Neonatal intoxication to vitamin D in premature babies: a series of16 cases. Arch Pediatr 2017;24:817-24.
  • 114 Salle BL, Delvin EE, Lapillonne A, et al. Perinatal metabolism of vitamin D. Am J Clin Nutr2000;71(Suppl):1317S-24S.
  • 115 Hibbs AM, Ross K, Kerns LA, et al. Effect of Vitamin D supplementation on recurrent wheezing in black infants who were born preterm: the D-Wheeze randomized clinical trial. JAMA2018;319:2086-94.
  • 116 Saintonge S, Bang H, Gerber LM. Implications of a new definition of vitamin D deficiency in a multiracial us adolescent population: the National Health and Nutrition Examination Survey III. Pediatrics 2009;123:797-803.
  • 117 Nielson CM, Jones KS, Chun RF, Jacobs JM, et al. Free 25-hydroxyvitamin D: impact of vitamin D binding protein assays on racial-genotypic associations. J Clin Endocrinol Metab 2016;101:2226-34.
  • 118 Denburg MR, Kalkwarf HJ, de Boer IH, et al. Vitamin D bioavailability and catabolism in pediatric chronic kidney disease. Pediatr Nephrol Berl Ger 2013;28: 1843-53.
  • 119 Bacchetta J, Bardet C, Prié D. Physiology of FGF23 and overview of genetic diseases associated with renal phosphate wasting. Metabolism 2020(103S):153865.
  • 120 Bouillon R, Schuit F, Antonio L, et al. Vitamin D binding protein: a historic overview. Front Endocrinol 2019;10:910.
  • 121 Schlingmann KP, Kaufmann M, Weber S, et al. Mutations in CYP24A1 and idiopathic infantile hypercalcemia. N Engl J Med 2011;365:410-21.
  • 122 Bailey D, Perumal N, Yazdanpanah M, et al. Maternal-fetal-infant dynamics of the C3-epimerof25-hydroxyvitamin D. Clin Biochem 2014;47:816-22.
  • 123 Fleet JC. The role of vitamin D in the endocrinology controlling calcium homeostasis. Mol Cell Endocrinol 2017;453:36-45.


VitaminDWiki - Consensus Vitamin D category

68 Vitamin D consensus publications

VitaminDWiki - Infant-Child category has 823 items

Having a good level of vitamin D cuts in half the amount of:

Need even more IUs of vitamin D to get a good level if;

  • Have little vitamin D: premie, twin, mother did not get much sun access
  • Get little vitamin D: dark skin, little access to sun
  • Vitamin D is consumed faster than normal due to sickness
  • Older (need at least 100 IU/kilogram, far more if obese)
  • Not get any vitamin D from formula (breast fed) or (fortified) milk
    Note – formula does not even provide 400 IU of vitamin D daily

Infants-Children need Vitamin D

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