» Articles » PMID: 30721411

Serum 25-hydroxyvitamin D Response to Vitamin D Supplementation in Infants: a Systematic Review and Meta-analysis of Clinical Intervention Trials

Overview
Journal Eur J Nutr
Date 2019 Feb 6
PMID 30721411
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: For the prevention of nutritional rickets, 400 IU vitamin D daily and circulating 25-hydroxyvitamin D (25OHD) concentrations > 50 nmol/L are recommended, whereas the toxicity threshold is set at 250 nmol/L. We synthesized the evidence for the effect of vitamin D supplementation on incremental 25OHD in infants up to 1 year of age.

Methods: We performed a systematic review and meta-analysis of intervention trials in several databases. A total of 87 records were identified for full-text review and 27 articles with 61 studies were included in the final analysis.

Results: The selected 61 studies included 1828 participants. Nineteen cohorts had already mean baseline 25OHD levels ≥ 50 nmol/L. The weighted mean difference in 25OHD following vitamin D supplementation was + 49.4 nmol/L (95% CI 43.6-55.3 nmol/L; P < 0.001). The increment was dose-dependent (P = 0.002), was higher in full-term than in pre-term infants (P < 0.001), was higher in infants with baseline 25OHD < 50 nmol/L as compared to ≥ 50 nmol/L (P = 0.001), and was marginally influenced by the 25OHD test procedure (P = 0.080). Vitamin D doses of 400 IU/day were sufficient to achieve 25OHD concentrations ≥ 50 nmol/L in most full-term infants. A 25OHD level of 250 nmol/L was not exceeded in ≥ 97.5% of infants at doses between 200 and 1200 IU/day, but potentially in ≥ 2.5% of infants at a dose of 1600 IU/day.

Conclusions: Vitamin D supplementation of 400 IU/day is sufficient for achieving 25OHD concentrations able to prevent nutritional rickets. A more personalized vitamin D dosing strategy would require 25OHD testing, but also assay standardization.

Citing Articles

Cord blood vitamin A and vitamin D levels in relation to physical growth in exclusively breastfed infants aged 0-6 months.

Zhao W, Li C, Shen W, Li K, Cai Y, Li F Front Endocrinol (Lausanne). 2024; 15:1394408.

PMID: 39129921 PMC: 11310037. DOI: 10.3389/fendo.2024.1394408.


Vitamin A, D, E, and K as Matrix Metalloproteinase-2/9 Regulators That Affect Expression and Enzymatic Activity.

Vo H, Nguyen Y, Kim N, Lee H Int J Mol Sci. 2023; 24(23).

PMID: 38069361 PMC: 10707015. DOI: 10.3390/ijms242317038.


Approach to Rickets: Is It Calciopenic or Phosphopenic?.

Abseyi S, Siklar Z Turk Arch Pediatr. 2023; 58(5):458-466.

PMID: 37427438 PMC: 10543743. DOI: 10.5152/TurkArchPediatr.2023.23050.


Effect of Vitamin D Supplementation on (25(OH)D) Status in Children 12-30 Months of Age: A Randomized Clinical Trial.

Flores-Aldana M, Rivera-Pasquel M, Garcia-Guerra A, Perez-Cortes J, Barcena-Echegollen J Nutrients. 2023; 15(12).

PMID: 37375660 PMC: 10304884. DOI: 10.3390/nu15122756.


Vitamin D supplementation improved physical growth and neurologic development of Preterm Infants receiving Nesting Care in the neonatal Intensive Care Unit.

Tang W, Ma N, Meng L, Luo Y, Wang Y, Zhang D BMC Pediatr. 2023; 23(1):248.

PMID: 37210477 PMC: 10199597. DOI: 10.1186/s12887-023-04075-1.


References
1.
Anderson-Berry A, Thoene M, Wagner J, Lyden E, Jones G, Kaufmann M . 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(10):e0185950. PMC: 5634602. DOI: 10.1371/journal.pone.0185950. View

2.
Abitbol C, DeFreitas M, Strauss J . Assessment of kidney function in preterm infants: lifelong implications. Pediatr Nephrol. 2016; 31(12):2213-2222. DOI: 10.1007/s00467-016-3320-x. View

3.
Macaskill P, Walter S, Irwig L . A comparison of methods to detect publication bias in meta-analysis. Stat Med. 2001; 20(4):641-54. DOI: 10.1002/sim.698. View

4.
Spiro A, Buttriss J . Vitamin D: An overview of vitamin D status and intake in Europe. Nutr Bull. 2015; 39(4):322-350. PMC: 4288313. DOI: 10.1111/nbu.12108. View

5.
Sterne J, Hernan M, Reeves B, Savovic J, Berkman N, Viswanathan M . ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ. 2016; 355:i4919. PMC: 5062054. DOI: 10.1136/bmj.i4919. View