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The chromosome 3q25 locus associated with fetal adiposity is not associated with childhood adiposity

机译:与胎儿肥胖相关的3q25染色体位点与儿童肥胖无关

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摘要

Increased newborn adiposity is associated with later adverse metabolic outcomes. Previous genome-wide association studies (GWAS) demonstrated strong association of a locus on chromosome 3 (3q25.31) with newborn sum of skinfolds, a measure of overall adiposity. Whether this locus is associated with childhood adiposity is unknown. Genotype and sum of skinfolds data were available for 293 children at birth and age 2, and for 350 children at birth and age 6 from a European cohort (Belfast, UK) who participated in the Hyperglycemia and Adverse Pregnancy Outcome GWAS. We examined single nucleotide polymorphisms (SNPs) at the 3q25.31 locus associated with newborn adiposity. Linear regression analyses under an additive genetic model adjusting for maternal body mass index were performed. In both cohorts, a positive association was observed between all SNPs and sum of skinfolds at birth (P=2.3 × 10−4, β=0.026 and P=4.8 × 10−4, β=0.025). At the age of 2 years, a non-significant negative association was observed with sum of skinfolds (P=0.06; β =−0.015). At the age of 6 years, there was no evidence of association (P=0.86; β=0.002). The 3q25.31 locus strongly associated with newborn adiposity had no significant association with childhood adiposity suggesting that its impact may largely be limited to fetal fat accretion.
机译:新生儿肥胖增加与以后不良的代谢结果有关。先前的全基因组关联研究(GWAS)表明,染色体3(3q25.31)上的一个位点与新生儿皮褶之和(整体肥胖的度量)有很强的关联。这个基因是否与儿童肥胖有关。来自293名参加高血糖症和不良妊娠结局GWAS的欧洲队列(英国贝尔法斯特)的293名2岁以下儿童的基因型和皮褶总和数据可用。我们检查了与新生儿肥胖相关的3q25.31位点的单核苷酸多态性(SNP)。在调整了孕产妇体重指数的加性遗传模型下进行了线性回归分析。在这两个队列中,所有SNP与出生时的皮肤皱褶总和之间均呈正相关(P = 2.3×10 −4 ,β= 0.026和P = 4.8×10 −4 ,β= 0.025)。在2岁时,与皮褶的总和之间没有显着的负相关(P = 0.06;β= -0.015)。在6岁时,没有关联的证据(P = 0.86;β= 0.002)。与新生儿肥胖症密切相关的3q25.31位点与儿童肥胖症没有显着关联,表明其影响可能很大程度上限于胎儿脂肪的积聚。

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