Effects of a combined micronutrient supplementation on maternal biological status and newborn anthropometrics measurements: a randomized double-blind, placebo-controlled trial in apparently healthy pregnant women
- 15 December 2003
- journal article
- clinical trial
- Published by Springer Nature in European Journal of Clinical Nutrition
- Vol. 58 (1) , 52-59
- https://doi.org/10.1038/sj.ejcn.1601745
Abstract
Objective: To investigate the possible beneficial effects of a micronutrient supplementation to apparently healthy pregnant women on maternal biological status and new born anthropometric characteristics. Setting: Departments of Obstetric of the University Hospital of Grenoble (France) and Lyon (France), Laboratoire of Biology of Oxidative Stress, UFR de Pharmacie. Grenoble (France). Study design: Double-blind, randomized placebo-controlled intervention trial. Subjects: A total of 100 apparently healthy pregnant women were recruited at 142 weeks of gestation to delivery. At the end, they were 65 women to follow out the study. Interventions: Daily consumption over gestation of a miconutrients supplement or placebo. Main outcome measures: Plasma micronutrient levels and oxidative stress parameters were measured in mothers at 14 and 38 weeks of gestation. New born's anthropometric characteristics were measured at delivery. Results: In the supplemented group, folic acid, vitamin C, E, B2, B6 and -carotene levels were higher than in the placebo group. Oxidative stress parameters were not different between the groups. Birth weights were increased by 10% and the number of low newborn weights (<2700g) decreased significantly when the mother received the supplementation. Maternal plasma Zn levels were positively correlated to the newborn heights. Conclusion: A regular intake of a micronutrient supplement at nutritional dose may be sufficient to improve micronutrient status of apparently healthy pregnant women and could prevent low birth weight of newborn. Sponsorship: The supplement and placebo were supplied and the study was partially funded by BOIRON Pharmaceutical Company.Keywords
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