Pregnancy vitamin D supplementation and offspring bone mineral density in childhood Follow-up of a randomised controlled trial.

IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS
Rebecca J Moon, Stefania D' Angelo, Elizabeth M Curtis, Kate A Ward, Sarah R Crozier, Inez Schoenmakers, M Kassim Javaid, Nicholas J Bishop, Keith M Godfrey, Cyrus Cooper, Nicholas C Harvey
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引用次数: 0

Abstract

Background: Findings from the MAVIDOS trial demonstrated a positive effect of gestational cholecalciferol supplementation on offspring bone mineral density (BMD) at age 4 years. Demonstrating persistence of this effect is important to understanding whether maternal vitamin D supplementation could be a useful public health strategy to improving bone health.

Objective: We investigated whether gestational vitamin D supplementation increases offspring BMD at 6-7 years in an exploratory post-hoc analysis of an existing trial.

Methods: In the MAVIDOS randomised controlled trial, pregnant females <14 weeks' gestation with a singleton pregnancy and serum 25-hydroxyvitamin D [25(OH)D] 25-100nmol/l at three UK hospitals (Southampton, Sheffield and Oxford) were randomised to either 1000 IU/day cholecalciferol or placebo from 14-17 weeks gestation until delivery. Offspring born at term to participants recruited in Southampton were invited to the childhood follow-up at 4 and 6-7 years. The children had a dual-energy X-ray absorptiometry (DXA, Hologic discovery) scan of whole-body-less-head (WBLH) and lumbar spine, from which bone area [BA], bone mineral content [BMC], BMD and bone mineral apparent density [BMAD]) were derived. Linear regression was used to compare the two groups adjusting for age, sex, height, weight, duration of consumption of human milk and vitamin D use at 6-7 years.

Results: 454 children were followed up at age 6-7 years, of whom 447 had a usable DXA scan. Gestational cholecalciferol supplementation resulted in higher WBLH BMC (0.15 SD, 95%CI 0.04, 0.26), BMD (0.18 SD, 95%CI 0.06,0.31), BMAD (0.18 SD, 95%CI 0.04,0.32) and lean mass (0.09 SD, 95%CI 0.00,0.17) compared to placebo. The effect of pregnancy cholecalciferol on bone outcomes was similar at ages 4 and 6-7 years.

Conclusions and relevance: Supplementation with cholecalciferol 1000 IU/day during pregnancy resulted in greater offspring BMD and lean mass in mid-childhood versus placebo in this exploratory post-hoc analysis. These findings suggest that pregnancy vitamin D supplementation may be an important population health strategy to improve bone health.

Trial registration: ISRCTN:82927713 https://doi.org/10.1186/ISRCTN82927713; EUDRACT:2007-001716-23 https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001716-23/results.

妊娠期维生素 D 补充剂与后代儿童期骨矿物质密度 随机对照试验的后续研究。
背景:MAVIDOS试验结果表明,妊娠期补充胆钙化醇对4岁后代的骨矿物质密度(BMD)有积极影响。证明这种效应的持续性对于了解母体补充维生素 D 是否是改善骨骼健康的有效公共卫生策略非常重要:我们在对一项现有试验进行的探索性事后分析中,研究了妊娠期补充维生素 D 是否会增加后代 6-7 岁时的 BMD:方法:在 MAVIDOS 随机对照试验中,对怀孕女性 结果:454 名儿童在 6-7 岁时接受了随访:454 名儿童在 6-7 岁时接受了随访,其中 447 人接受了可用的 DXA 扫描。与安慰剂相比,妊娠期补充胆钙化醇可提高 WBLH BMC(0.15 SD,95%CI 0.04,0.26)、BMD(0.18 SD,95%CI 0.06,0.31)、BMAD(0.18 SD,95%CI 0.04,0.32)和瘦体重(0.09 SD,95%CI 0.00,0.17)。妊娠期胆钙化醇对4岁和6-7岁儿童骨骼发育的影响相似:在这项探索性事后分析中,与安慰剂相比,孕期补充胆钙化醇 1000 IU/天可使后代在儿童中期的BMD和瘦体重增加。这些研究结果表明,孕期补充维生素D可能是改善骨骼健康的重要人群保健策略:ISRCTN:82927713 https://doi.org/10.1186/ISRCTN82927713; EUDRACT:2007-001716-23 https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-001716-23/results.
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来源期刊
CiteScore
12.40
自引率
4.20%
发文量
332
审稿时长
38 days
期刊介绍: American Journal of Clinical Nutrition is recognized as the most highly rated peer-reviewed, primary research journal in nutrition and dietetics.It focuses on publishing the latest research on various topics in nutrition, including but not limited to obesity, vitamins and minerals, nutrition and disease, and energy metabolism. Purpose: The purpose of AJCN is to: Publish original research studies relevant to human and clinical nutrition. Consider well-controlled clinical studies describing scientific mechanisms, efficacy, and safety of dietary interventions in the context of disease prevention or health benefits. Encourage public health and epidemiologic studies relevant to human nutrition. Promote innovative investigations of nutritional questions employing epigenetic, genomic, proteomic, and metabolomic approaches. Include solicited editorials, book reviews, solicited or unsolicited review articles, invited controversy position papers, and letters to the Editor related to prior AJCN articles. Peer Review Process: All submitted material with scientific content undergoes peer review by the Editors or their designees before acceptance for publication.
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