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Basal Vitamin D Status and Supplement Dose Are Primary Contributors to Maternal 25-Hydroxyvitamin D Response to Prenatal and Postpartum Cholecalciferol Supplementation.
Levy, Benjamin; O'Callaghan, Karen M; Qamar, Huma; Mahmud, Abdullah Al; Gernand, Alison D; Islam, M Munirul; Roth, Daniel E.
Afiliación
  • Levy B; Centre for Global Child Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • O'Callaghan KM; Centre for Global Child Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Qamar H; Centre for Global Child Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Mahmud AA; Nutrition and Clinical Services Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr, b), Dhaka, Bangladesh.
  • Gernand AD; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, USA.
  • Islam MM; Nutrition and Clinical Services Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr, b), Dhaka, Bangladesh.
  • Roth DE; Centre for Global Child Health, Hospital for Sick Children, Toronto, Ontario, Canada.
J Nutr ; 151(11): 3361-3378, 2021 11 02.
Article en En | MEDLINE | ID: mdl-34302350
ABSTRACT

BACKGROUND:

Variability in the 25-hydroxyvitamin D [25(OH)D] response to prenatal and postpartum vitamin D supplementation is an important consideration for establishing vitamin D deficiency prevention regimens.

OBJECTIVES:

We aimed to examine interindividual variation in maternal and infant 25(OH)D following maternal vitamin D supplementation.

METHODS:

In a randomized trial of maternal vitamin D supplementation (Maternal Vitamin D for Infant Growth Trial), healthy pregnant women (n = 1300) received a prenatal cholecalciferol (vitamin D-3) dose of 0, 4200, 16,800, or 28,000 IU/wk from 17 to 24 wk of gestation followed by placebo to 6 mo postpartum. A fifth group received 28,000 IU cholecalciferol/wk both prenatally and postpartum. In a subset of participants, associations of 25(OH)D with hypothesized explanatory factors were estimated in women at delivery (n = 655) and 6 mo postpartum (n = 566), and in their infants at birth (n = 502) and 6 mo of age (n = 215). Base models included initial 25(OH)D and supplemental vitamin D dose. Multivariable models were extended to include other individual characteristics and specimen-related factors. The model coefficient of determination (R2) was used to express the percentage of total variance explained.

RESULTS:

Supplemental vitamin D intake and initial 25(OH)D accounted for the majority of variance in maternal 25(OH)D at delivery and postpartum (R2 = 70% and 79%, respectively). Additional characteristics, including BMI, contributed negligibly to remaining variance (<5% increase in R2). Variance in neonatal 25(OH)D was explained mostly by maternal delivery 25(OH)D and prenatal vitamin D intake (R2 = 82%). Variance in 25(OH)D in later infancy could only partly be explained by numerous biological, sociodemographic, and laboratory-related characteristics, including feeding practices (R2 = 43%).

CONCLUSIONS:

Presupplementation 25(OH)D and vitamin D supplemental dose are the major determinants of the response to maternal prenatal vitamin D intake. Vitamin D dosing regimens to prevent maternal and infant vitamin D deficiency should take into consideration the mean 25(OH)D concentration of the target population.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deficiencia de Vitamina D / Colecalciferol Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: J Nutr Año: 2021 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deficiencia de Vitamina D / Colecalciferol Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: J Nutr Año: 2021 Tipo del documento: Article País de afiliación: Canadá