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Genetic determinants of BMI from early childhood to adolescence: the Santiago Longitudinal Study

机译:幼年早期BMI遗传决定因素:Santiago纵向研究

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Background While the genetic contribution to obesity is well established, few studies have examined how genetic variants influence standardized body mass index Z‐score (BMIz) in Hispanics/Latinos, especially across childhood and adolescence. Objectives We estimated the effect of established BMIz loci in Chilean children of the Santiago Longitudinal Study (SLS). Methods We examined associations with BMIz at age 10 for 15 loci previously identified in European children. For significant loci, we performed association analyses at ages 5 and 16 years, for which we have smaller sample sizes. We tested associations of unweighted genetic risk scores (GRSs) for previously identified tag variants (GRS_EUR) and from the most significant variants in SLS at each locus (GRS_SLS). Results We generalized five variants at age 10 (P < 0.05 and directionally consistent), including rs543874 that reached Bonferroni‐corrected significance. The effect on BMIz was greatest at age 10 for all significant loci, except FTO, which exhibited an increase in effect from ages 5 to 16. Both GRSs were associated with BMIz (P < 0.0001), but GRS_SLS explained a much greater proportion of the variation (13.63%). Conclusion Our results underscore the importance of conducting genetic investigations across life stages and selecting ancestry appropriate tag variants in future studies for disease prediction and clinical evaluation.
机译:背景技术虽然对肥胖的遗传贡献得到明确,但很少有研究检测了遗传变异如何影响西班牙语/拉丁裔的标准化体重指数Z-得分(BMIZ),特别是在儿童期和青春期。目的我们估计了圣地亚哥纵向研究(SLS)智利儿童的建立BMIZ基因座的效果。方法我们在欧洲儿童中确定的15岁的10岁左右的10岁的方法审查了与BMIT的协会。对于重要的基因座,我们执行了5岁及16岁的关联分析,我们具有较小的样本尺寸。我们测试了未加权的遗传风险评分(GRS)对先前鉴定的标签变体(GRS_eur)的关联,以及每个基因座(GRS_SL)的SLS中最重要的变体。结果我们在10岁时推广了五种变体(P <0.05和方向一致),包括RS5438​​74,达到了Bonferroni校正的意义。除FTO外,对所有重要基因座的10岁时对BMIZ的影响最大,除了FTO,从5至16岁的效果增加。两个GRS与BMIZ相关(P <0.0001),但GRS_SLS解释了更大的比例变异(13.63%)。结论我们的结果强调了在未来疾病预测和临床评价的研究中进行终身阶段进行遗传调查和选择祖先适当的标签变体的重要性。

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