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Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother–infant pairs

机译:对母体表型,出生结果和成人表型之间的关联相关妇幼和胎儿遗传效应:10,734母婴对中的孟德利随机化和单倍型遗传分数分析

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Background Many maternal traits are associated with a neonate’s gestational duration, birth weight, and birth length. These birth outcomes are subsequently associated with late-onset health conditions. The causal mechanisms and the relative contributions of maternal and fetal genetic effects behind these observed associations are unresolved. Methods and findings Based on 10,734 mother–infant duos of European ancestry from the UK, Northern Europe, Australia, and North America, we constructed haplotype genetic scores using single-nucleotide polymorphisms (SNPs) known to be associated with adult height, body mass index (BMI), blood pressure (BP), fasting plasma glucose (FPG), and type 2 diabetes (T2D). Using these scores as genetic instruments, we estimated the maternal and fetal genetic effects underlying the observed associations between maternal phenotypes and pregnancy outcomes. We also used infant-specific birth weight genetic scores as instrument and examined the effects of fetal growth on pregnancy outcomes, maternal BP, and glucose levels during pregnancy. The maternal nontransmitted haplotype score for height was significantly associated with gestational duration (p = 2.2 × 10?4). Both maternal and paternal transmitted height haplotype scores were highly significantly associated with birth weight and length (p 1 × 10?17). The maternal transmitted BMI scores were associated with birth weight with a significant maternal effect (p = 1.6 × 10?4). Both maternal and paternal transmitted BP scores were negatively associated with birth weight with a significant fetal effect (p = 9.4 × 10?3), whereas BP alleles were significantly associated with gestational duration and preterm birth through maternal effects (p = 3.3 × 10?2 and p = 4.5 × 10?3, respectively). The nontransmitted haplotype score for FPG was strongly associated with birth weight (p = 4.7 × 10?6); however, the glucose-increasing alleles in the fetus were associated with reduced birth weight through a fetal effect (p = 2.2 × 10?3). The haplotype scores for T2D were associated with birth weight in a similar way but with a weaker maternal effect (p = 6.4 × 10?3) and a stronger fetal effect (p = 1.3 × 10?5). The paternal transmitted birth weight score was significantly associated with reduced gestational duration (p = 1.8 × 10?4) and increased maternal systolic BP during pregnancy (p = 2.2 × 10?2). The major limitations of the study include missing and heterogenous phenotype data in some data sets and different instrumental strength of genetic scores for different phenotypic traits. Conclusions We found that both maternal height and fetal growth are important factors in shaping the duration of gestation: genetically elevated maternal height is associated with longer gestational duration, whereas alleles that increase fetal growth are associated with shorter gestational duration. Fetal growth is influenced by both maternal and fetal effects and can reciprocally influence maternal phenotypes: taller maternal stature, higher maternal BMI, and higher maternal blood glucose are associated with larger birth size through maternal effects; in the fetus, the height- and metabolic-risk–increasing alleles are associated with increased and decreased birth size, respectively; alleles raising birth weight in the fetus are associated with shorter gestational duration and higher maternal BP. These maternal and fetal genetic effects may explain the observed associations between the studied maternal phenotypes and birth outcomes, as well as the life-course associations between these birth outcomes and adult phenotypes.
机译:背景技术许多母体特征与新生儿的妊娠期,出生体重和出生长度有关。这些出生结果随后与晚期健康状况相关。这些观察到的关联背后母亲和胎儿遗传效应的因果机制和相对贡献是未解决的。根据英国,北欧,澳大利亚和北美的欧洲祖先母婴二重奏的方法和调查结果,我们用已知与成人高度,体重指数相关的单核苷酸多态性(SNP)构建单倍型遗传分数(BMI),血压(BP),空腹血浆葡萄糖(FPG)和2型糖尿病(T2D)。使用这些分数作为遗传仪器,我们估计母体表型和妊娠结果之间观察到的关联潜在的母体和胎儿遗传效果。我们还将婴儿特异性出生体重遗传分数作为仪器,并检测胎儿生长对妊娠期妊娠孕产阶级,母体BP和葡萄糖水平的影响。高度的母体非扫描的单倍型评分与妊娠期持续时间显着相关(P = 2.2×10?4)。母体和父亲和父亲透射高度单倍型分数与出生体重和长度高度显着相关(P <1×10?17)。母体传播的BMI分数与出生体重相关,具有显着的母体效果(P = 1.6×10?4)。母亲和父亲和父亲和父亲透射的BP分数与出生体重呈负相关,具有显着的胎儿效应(p = 9.4×10?3),而BP等位基因通过母体效应与妊娠期持续时间和早产有显着相关(P = 3.3×10? 2和p = 4.5×10?3分别)。 FPG的非扫描单倍型评分与出生体重强烈相关(P = 4.7×10?6);然而,胎儿中的葡萄糖增加的等位基因与胎儿效应的出生体重降低(P = 2.2×10?3)相关。 T2D的单倍型评分以类似的方式与出生体重相关,但母体效果较弱(P = 6.4×10?3)和更强的胎效(P = 1.3×10?5)。父亲传播的出生体重分数显着与妊娠期持续时间(P = 1.8×10?4)显着相关,并在妊娠期间增加母体收缩性BP(P = 2.2×10?2)。该研究的主要局限性包括一些数据集中的缺失和异源表型数据以及不同表型性状的遗传分数的不同毒性强度。结论我们发现母体高度和胎儿生长都是塑造妊娠期持续时间的重要因素:基因升高的孕产量与妊娠期持续时间更长,而增加胎儿生长的等位基因与较短的妊娠期相关。胎儿生长受孕产妇和胎儿效应的影响,可以相互影响母体表型:较高的母体身高,较高的母体BMI和更高的母体血糖与通过母体效应的较大的出生尺寸相关;在胎儿中,高度和代谢风险的增加的等位基因分别与出生尺寸的增加和降低有关;提高胎儿出生体重的等位基因与较短的妊娠期和更高的母体BP相关。这些母亲和胎儿遗传效应可以解释所观察到的母体表型和出生结果之间的关联,以及这些出生结果和成人表型之间的生命课程协会。

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