Prenatal vitamin D and cord blood insulin-like growth factors in Dhaka, Bangladesh.

IGF axis fetal growth pregnancy vitamin D

Journal

Endocrine connections
ISSN: 2049-3614
Titre abrégé: Endocr Connect
Pays: England
ID NLM: 101598413

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 27 04 2019
accepted: 07 05 2019
pubmed: 10 5 2019
medline: 10 5 2019
entrez: 10 5 2019
Statut: ppublish

Résumé

Fetal growth restriction is linked to adverse health outcomes and is prevalent in low- and middle-income countries; however, determinants of fetal growth are still poorly understood. The objectives were to determine the effect of prenatal vitamin D supplementation on the insulin-like growth factor (IGF) axis at birth, to compare the concentrations of IGF-I in newborns in Bangladesh to a European reference population and to estimate the associations between IGF protein concentrations and birth size. In a randomized controlled trial in Dhaka, Bangladesh, pregnant women enrolled at 17-24 weeks of gestation were assigned to weekly oral vitamin D3 supplementation from enrolment to delivery at doses of 4200 IU/week, 16,800 IU/week, 28,000 IU/week or placebo. In this sub-study, 559 woman-infant pairs were included for analysis and cord blood IGF protein concentrations were quantified at birth. There were no significant effects of vitamin D supplementation on cord blood concentrations of IGF-I (P = 0.398), IGF-II (P = 0.525), binding proteins (BPs) IGFBP-1 (P = 0.170), IGFBP-3 (P = 0.203) or the molar ratio of IGF-I/IGFBP-3 (P = 0.941). In comparison to a European reference population, 6% of girls and 23% of boys had IGF-I concentrations below the 2.5th percentile of the reference population. IGF-I, IGF-II, IGFBP-3 and the IGF-I/IGFBP-3 ratio were positively associated with at least one anthropometric parameter, whereas IGFBP-1 was negatively associated with birth anthropometry. In conclusion, prenatal vitamin D supplementation does not alter or enhance fetal IGF pathways.

Identifiants

pubmed: 31071681
doi: 10.1530/EC-19-0123
pii: EC-19-0123.R1
pmc: PMC6547305
doi:
pii:

Types de publication

Journal Article

Langues

eng

Pagination

745-753

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Auteurs

Monika Bilic (M)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.
Department of Nutritional Sciences, University of Toronto, Toronto, Canada.

Huma Qamar (H)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.
Department of Nutritional Sciences, University of Toronto, Toronto, Canada.

Akpevwe Onoyovwi (A)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.

Jill Korsiak (J)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.

Eszter Papp (E)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.

Abdullah Al Mahmud (A)

Nutrition and Clinical Services Division, icddr,b, Dhaka, Bangladesh.

Rosanna Weksberg (R)

Genetics and Genome Biology, Hospital for Sick Children, Toronto, Canada.
Molecular and Medical Genetics, University of Toronto, Toronto, Canada.
Department of Paediatrics, Hospital for Sick Children and University of Toronto, Toronto, Canada.

Alison D Gernand (AD)

Department of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania, USA.

Jennifer Harrington (J)

Division of Endocrinology, Hospital for Sick Children, Toronto, Canada.

Daniel E Roth (DE)

Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.
Department of Nutritional Sciences, University of Toronto, Toronto, Canada.
Department of Paediatrics, Hospital for Sick Children and University of Toronto, Toronto, Canada.

Classifications MeSH