Evaluation of multiple micronutrient supplementation and medium-quantity lipid-based nutrient supplementation in pregnancy on child development in rural Niger: A secondary analysis of a cluster randomized controlled trial

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL PLoS Medicine Pub Date : 2022-05-01 DOI:10.1371/journal.pmed.1003984
C. Sudfeld, L. Bliznashka, Aichatou Salifou, O. Guindo, Issaka Soumana, Irène Adehossi, C. Langendorf, R. Grais, Sheila Isanaka
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Abstract

Background It is estimated that over 250 million children under 5 years of age in low- and middle-income countries (LMICs) do not reach their full developmental potential. Poor maternal diet, anemia, and micronutrient deficiencies during pregnancy are associated with suboptimal neurodevelopmental outcomes in children. However, the effect of prenatal macronutrient and micronutrient supplementation on child development in LMIC settings remains unclear due to limited evidence from randomized trials. Methods and findings We conducted a 3-arm cluster-randomized trial (n = 53 clusters) that evaluated the efficacy of (1) prenatal multiple micronutrient supplementation (MMS; n = 18 clusters) and (2) lipid-based nutrient supplementation (LNS; n = 18 clusters) as compared to (3) routine iron–folic acid (IFA) supplementation (n = 17 clusters) among pregnant women in the rural district of Madarounfa, Niger, from March 2015 to August 2019 (ClinicalTrials.gov identifier NCT02145000). Children were followed until 2 years of age, and the Bayley Scales of Infant and Toddler Development III (BSID-III) were administered to children every 3 months from 6 to 24 months of age. Maternal report of WHO gross motor milestone achievement was assessed monthly from 3 to 24 months of age. An intention-to-treat analysis was followed. Child BSID-III data were available for 559, 492, and 581 singleton children in the MMS, LNS, and IFA groups, respectively. Child WHO motor milestone data were available for 691, 781, and 753 singleton children in the MMS, LNS, and IFA groups, respectively. Prenatal MMS had no effect on child BSID-III cognitive (standardized mean difference [SMD]: 0.21; 95% CI: −0.20, 0.62; p = 0.32), language (SMD: 0.16; 95% CI: −0.30, 0.61; p = 0.50) or motor scores (SMD: 0.18; 95% CI: −0.39, 0.74; p = 0.54) or on time to achievement of the WHO gross motor milestones as compared to IFA. Prenatal LNS had no effect on child BSID-III cognitive (SMD: 0.17; 95% CI: −0.15, 0.49; p = 0.29), language (SMD: 0.11; 95% CI: −0.22, 0.44; p = 0.53) or motor scores (SMD: −0.04; 95% CI: −0.46, 0.37; p = 0.85) at the 24-month endline visit as compared to IFA. However, the trajectory of BSID-III cognitive scores during the first 2 years of life differed between the groups with children in the LNS group having higher cognitive scores at 18 and 21 months (approximately 0.35 SD) as compared to the IFA group (p-value for difference in trajectory <0.001). Children whose mothers received LNS also had earlier achievement of sitting alone (hazard ratio [HR]: 1.57; 95% CI: 1.10 to 2.24; p = 0.01) and walking alone (1.52; 95% CI: 1.14 to 2.03; p = 0.004) as compared to IFA, but there was no effect on time to achievement of other motor milestones. A limitation of our study is that we assessed child development up to 2 years of age, and, therefore, we may have not captured effects that are easier to detect or emerge at older ages. Conclusions There was no benefit of prenatal MMS on child development outcomes up to 2 years of age as compared to IFA. There was evidence of an apparent positive effect of prenatal LNS on cognitive development trajectory and time to achievement of selected gross motor milestones. Trial registration ClinicalTrials.gov NCT02145000.
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评估多种微量营养素补充和中等量的脂质营养补充在怀孕期间对尼日尔农村儿童发育的影响:一项聚类随机对照试验的二次分析
背景据估计,在中低收入国家,有超过2.5亿5岁以下的儿童没有充分发挥其发展潜力。母亲饮食不良、贫血和妊娠期微量营养素缺乏与儿童神经发育不良有关。然而,由于随机试验的证据有限,产前补充大量营养素和微量营养素对LMIC环境中儿童发育的影响尚不清楚。方法和研究结果我们进行了一项3臂集群随机试验(n=53个集群),评估了(1)产前多种微量营养素补充(MMS;n=18个集群)和(2)基于脂质的营养补充(LNS;n=18集群)与(3)常规铁-叶酸补充(IFA)(n=17个集群)在农村地区孕妇中的疗效2015年3月至2019年8月,尼日尔Madarounfa(ClinicalTrials.gov标识符NCT02145000)。对儿童进行随访至2岁,并对6至24个月大的儿童每3个月进行一次贝利婴幼儿发育量表III(BSID-III)。世界卫生组织3至24个月大的产妇运动总里程碑成绩报告每月进行评估。随后进行意向治疗分析。儿童BSID-II数据可分别用于MMS、LNS和IFA组中的559、492和581名独生子女。世界卫生组织儿童运动里程碑数据可分别用于MMS组、NZ组和IFA组的691名、781名和753名独生子女。与IFA相比,产前MMS对儿童BSID-II认知(标准化平均差异[SMD]:0.21;95%CI:-0.20,0.62;p=0.32)、语言(SMD:0.16;95%CI:-0.30,0.61;p=0.50)或运动得分(SMD:0.18;95%CI:-0.39,0.74;p=0.54)或实现世界卫生组织总运动里程碑的时间没有影响。与IFA相比,产前LNS对24个月随访时儿童BSID-III认知能力(SMD:0.17;95%CI:-0.15,0.49;p=0.29)、语言(SMD:0.11;95%CI:-0.22,0.44;p=0.53)或运动评分(SMD:-0.04;95%CI:-0.46,0.37;p=0.85)没有影响。然而在生命的前2年,BSID-III认知得分的轨迹在两组之间存在差异,与IFA组相比,在18个月和21个月时,LNS组的儿童认知得分更高(约0.35 SD)(轨迹差异的p值<0.001)。母亲接受LNS的儿童也更早地实现了独自坐着(危险比[HR]:1.57;95%可信区间:1.10至2.24;p=0.01)和单独行走(1.52;95%置信区间:1.14至2.03;p=0.004),但对实现其他运动里程碑的时间没有影响。我们研究的一个局限性是,我们评估了2岁以下的儿童发育,因此,我们可能没有捕捉到更容易发现或在年龄较大时出现的影响。结论与IFA相比,产前MMS对2岁以下儿童的发育结果没有任何益处。有证据表明,产前LNS对认知发展轨迹和达到选定总运动里程碑的时间有明显的积极影响。试验注册ClinicalTrials.gov NCT02145000。
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来源期刊
PLoS Medicine
PLoS Medicine 医学-医学:内科
CiteScore
21.60
自引率
0.60%
发文量
227
审稿时长
3 months
期刊介绍: PLOS Medicine aims to be a leading platform for research and analysis on the global health challenges faced by humanity. The journal covers a wide range of topics, including biomedicine, the environment, society, and politics, that affect the well-being of individuals worldwide. It particularly highlights studies that contribute to clinical practice, health policy, or our understanding of disease mechanisms, with the ultimate goal of improving health outcomes in diverse settings. Unwavering in its commitment to ethical standards, PLOS Medicine ensures integrity in medical publishing. This includes actively managing and transparently disclosing any conflicts of interest during the reporting, peer review, and publication processes. The journal promotes transparency by providing visibility into the review and publication procedures. It also encourages data sharing and the reuse of published work. Author rights are upheld, allowing them to retain copyright. Furthermore, PLOS Medicine strongly supports Open Access publishing, making research articles freely available to all without restrictions, facilitating widespread dissemination of knowledge. The journal does not endorse drug or medical device advertising and refrains from exclusive sales of reprints to avoid conflicts of interest.
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