首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Maternal and offspring adiposity-related genetic variants and gestational weight gain.
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Maternal and offspring adiposity-related genetic variants and gestational weight gain.

机译:孕妇和后代肥胖相关的遗传变异和妊娠体重增加。

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摘要

BACKGROUND: Gestational weight gain (GWG) is associated with a range of health outcomes, but little is known about the factors that influence it. OBJECTIVE: The objective was to test the hypothesis that maternal and fetal genetic variants that are reliably associated with adiposity are associated with GWG. DESIGN: We examined the association of a risk allele score by using 4 adiposity-related single nucleotide polymorphisms (SNPs; rs9939609 in FTO, rs17782313 near MC4R, rs6548238 near TMEM18, and rs10938397 near GNPDA2) with GWG in a pregnancy cohort in which women had detailed repeated assessment of GWG (median number of weight measurements: 10; interquartile range: 8, 11). The numbers included in our analyses varied between 2324 and 7563 for different variant-outcome analyses. A linear spline random-effects model was used to model weight change with gestational age and to relate genetic variants to this. This modeling confirmed 3 distinct periods of GWG: 0-18, 19-28, and >/=29 wk of gestation. RESULTS: Maternal risk allele score and SNPs in FTO, MC4R, and TMEM18 were positively associated with prepregnancy weight. Maternal allele score was inversely associated with GWG in the first 18 wk of pregnancy (-14.46 g/wk per allele; 95% CI: -24.75, -4.17 g/wk per allele) but was not associated with other periods of GWG. Offspring allele score and maternal and offspring individual SNPs were not associated with GWG in any period or with birth weight or postnatal weight retention. CONCLUSIONS: Our findings suggest that neither maternal nor fetal adiposity-related genetic variants are associated with greater GWG. The inverse association of maternal allele score with GWG in the first 18 wk requires replication.
机译:背景:妊娠期体重增加(GWG)与一系列健康结果相关,但对其影响因素知之甚少。目的:目的是检验以下假设:与肥胖症可靠相关的母体和胎儿遗传变异与GWG相关。设计:我们通过使用4个与肥胖相关的单核苷酸多态性(SNP; FTO中的rs9939609,MC4R附近的rs17782313,TMEM18附近的rs6548238和GNPDA2附近的rs10938397)和4个肥胖人群的风险等位基因评分与GWG的关联GWG的详细重复评估(重量测量的中位数:10;四分位间距:8、11)。对于不同的变异结果分析,我们的分析中包含的数字在2324和7563之间变化。使用线性样条随机效应模型来模拟体重随胎龄的变化,并将遗传变异与此相关。该模型确定了GWG的3个不同时期:0-18、19-28和> / = 29 wk妊娠。结果:FTO,MC4R和TMEM18中的母亲风险等位基因评分和SNP与妊娠前体重呈正相关。孕妇等位基因得分与怀孕前18周的GWG呈负相关(每个等位基因-14.46 g / wk; 95%CI:-24.75,每个等位基因-4.17 g / wk),但与其他GWG时期无关。子代等位基因评分以及母体和子代个体SNP在任何时期均与GWG无关,也与出生体重或产后体重保持无关。结论:我们的发现表明,无论是母亲还是胎儿肥胖相关的遗传变异都与更大的GWG无关。在最初的18周内,母亲等位基因得分与GWG呈负相关,需要复制。

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