The effect of vitamin D supplementation and nutritional intake on skeletal maturity and bone health in socio-economically deprived children.


Journal

European journal of nutrition
ISSN: 1436-6215
Titre abrégé: Eur J Nutr
Pays: Germany
ID NLM: 100888704

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 08 06 2020
accepted: 05 02 2021
pubmed: 22 2 2021
medline: 13 8 2021
entrez: 21 2 2021
Statut: ppublish

Résumé

1. To determine the effect of vitamin D supplementation on bone age (BA), a marker of skeletal maturity, and Bone Health Index (BHI), a surrogate marker of bone density. 2. To characterise the differences in nutritional intake and anthropometry between children with advanced vs. delayed BA. The current study is a post hoc analysis of radiographs obtained as part of a randomised controlled trial. In this double-blind, placebo-controlled trial, deprived Afghan children (n = 3046) aged 1-11 months were randomised to receive six doses of oral placebo or vitamin D3 (100,000 IU) every 3 months for 18 months. Dietary intake was assessed through semi-quantitative food frequency questionnaires at two time points. Anthropometric measurements were undertaken at baseline and 18 months. Serum 25OHD was measured at five time points on a random subset of 632 children. Knee and wrist radiographs were obtained from a random subset (n = 641), of which 565 wrist radiographs were digitised for post-hoc analysis of BA and BHI using BoneXpert version 3.1. Nearly 93% (522, male = 291) of the images were analysable. The placebo (n = 258) and vitamin D (n = 264) groups were comparable at baseline. The mean (± SD) age of the cohort was 2 (± 0.3) years. At study completion, there was no difference in mean 25-hydroxy vitamin D concentrations [47 (95% CI 41, 56) vs. 55 (95% CI 45, 57) nmol/L, p = 0.2], mean (± SD) BA SDS [- 1.04 (1.36) vs. - 1.14 (1.26) years, p = 0.3] or mean (± SD) BHI SDS [- 0.30 (0.86) vs. - 0.31 (0.80), p = 0.8] between the placebo and vitamin D groups, respectively. Children with advanced skeletal maturity (BA SDS ≥ 0) when compared to children with delayed skeletal maturity (BA SDS < 0), had consumed more calories [mean (± SD) calories 805 (± 346) vs 723 (± 327) kcal/day, respectively, p < 0.05], were significantly less stunted (height SDS - 1.43 vs. - 2.32, p < 0.001) and underweight (weight SDS - 0.82 vs. - 1.45, p < 0.001), with greater growth velocity (11.57 vs 10.47 cm/ year, p < 0.05). Deprived children have significant delay in skeletal maturation but no substantial impairment in bone health as assessed by BHI. BA delay was influenced by total calorie intake, but not bolus vitamin D supplementation.

Identifiants

pubmed: 33611615
doi: 10.1007/s00394-021-02511-5
pii: 10.1007/s00394-021-02511-5
pmc: PMC8354903
doi:

Substances chimiques

Vitamin D 1406-16-2
Cholecalciferol 1C6V77QF41

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

3343-3353

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Development Partnership in higher education
ID : 53
Organisme : Wellcome Trust
ID : 082476/Z/07/Z
Pays : United Kingdom

Informations de copyright

© 2021. Crown.

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Auteurs

Suma Uday (S)

Department of Endocrinology and Diabetes, Birmingham Women's and Children's Hospital, Steelhouse lane, Birmingham, UK.
Institute of Metabolism and Systems Research, University of Birmingham, Edgbaston, Birmingham, UK.

Semira Manaseki-Holland (S)

Institute of Applied Health Research, University of Birmingham, Birmingham, UK. s.manasekiholland@bham.ac.uk.
College of Medical and Dental Sciences, University of Birmingham, Rm G31, Public Health Building, Edgbaston, Birmingham, B15 2TT, UK. s.manasekiholland@bham.ac.uk.

Jessica Bowie (J)

College of Medical and Dental Sciences, University of Birmingham, Rm G31, Public Health Building, Edgbaston, Birmingham, B15 2TT, UK.

Mohamed Zulf Mughal (MZ)

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK.

Francesca Crowe (F)

Institute of Applied Health Research, University of Birmingham, Birmingham, UK.

Wolfgang Högler (W)

Institute of Metabolism and Systems Research, University of Birmingham, Edgbaston, Birmingham, UK.
Department of Paediatrics and Adolescent Medicine, Johannes Kepler University, Linz, Austria.

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