Institute for Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
University of Queensland Diamantina Institute, University of Queensland, Woolloongabba, QLD, Australia.
Int J Epidemiol. 2021 Mar 3;50(1):179-189. doi: 10.1093/ije/dyaa256.
Lower maternal serum vitamin B12 (B12) and folate levels have been associated with lower offspring birthweight, in observational studies. The aim of this study was to investigate whether this relationship is causal.
We performed two-sample Mendelian randomization (MR) using summary data on associations between genotype-B12 (10 genetic variants) or genotype-folate (four genetic variants) levels from: a genome-wide association study of 45 576 individuals (sample 1); and both maternal- and fetal-specific genetic effects on offspring birthweight from the latest Early Growth Genetics consortium meta-analysis with 297 356 individuals reporting their own birthweight and 210 248 women reporting their offspring's birthweight (sample 2). We used the inverse variance weighted method, and sensitivity analyses to account for pleiotropy, in addition to excluding a potentially pleiotropic variant in the FUT2 gene for B12 levels.
We did not find evidence for a causal effect of maternal or fetal B12 levels on offspring birthweight. The results were consistent across the different methods. We found a positive causal effect of maternal folate levels on offspring birthweight [0.146 (0.065, 0.227), which corresponds to an increase in birthweight of 71 g per 1 standard deviation higher folate]. We found some evidence for a small inverse effect of fetal folate levels on their own birthweight [-0.051 (-0.100, -0.003)].
Our results are consistent with evidence from randomized controlled trials that higher maternal folate levels increase offspring birthweight. We did not find evidence for a causal effect of B12 levels on offspring birthweight, suggesting previous observational studies may have been confounded.
在观察性研究中,较低的母体血清维生素 B12(B12)和叶酸水平与较低的后代出生体重有关。本研究的目的是调查这种关系是否具有因果关系。
我们使用来自以下两个样本的基因型-B12(10 个遗传变异)或基因型-叶酸(4 个遗传变异)水平的汇总数据进行两样本 Mendelian 随机化(MR)分析:a) 45576 名个体的全基因组关联研究(样本 1);b) 最新的早期生长遗传学联盟荟萃分析中,母体和胎儿对后代出生体重的特异性遗传效应,该分析纳入了 297356 名报告自己出生体重的个体和 210248 名报告其子女出生体重的女性(样本 2)。我们使用逆方差加权法,并进行敏感性分析以排除 B12 水平中 FUT2 基因的潜在多效性变异。
我们没有发现母体或胎儿 B12 水平对后代出生体重有因果影响的证据。不同方法的结果一致。我们发现母体叶酸水平对后代出生体重有正向因果影响[0.146(0.065,0.227),这对应于叶酸水平每增加一个标准差,出生体重增加 71g]。我们发现胎儿叶酸水平对其自身出生体重有轻微的负向因果影响[-0.051(-0.100,-0.003)]。
我们的结果与随机对照试验的证据一致,即较高的母体叶酸水平可增加后代的出生体重。我们没有发现 B12 水平对后代出生体重有因果影响的证据,这表明之前的观察性研究可能存在混杂。