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The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts

机译:在几个但不是全部队列中都复制了INSIG2的SNP上游与体重指数的关联

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摘要

A SNP upstream of the INSIG2 gene, rs7566605, was recently found to be associated with obesity as measured by body mass index (BMI) by Herbert and colleagues. The association between increased BMI and homozygosity for the minor allele was first observed in data from a genome-wide association scan of 86,604 SNPs in 923 related individuals from the Framingham Heart Study offspring cohort. The association was reproduced in four additional cohorts, but was not seen in a fifth cohort. To further assess the general reproducibility of this association, we genotyped rs7566605 in nine large cohorts from eight populations across multiple ethnicities (total n = 16,969). We tested this variant for association with BMI in each sample under a recessive model using family-based, population-based, and case-control designs. We observed a significant (p < 0.05) association in five cohorts but saw no association in three other cohorts. There was variability in the strength of association evidence across examination cycles in longitudinal data from unrelated individuals in the Framingham Heart Study Offspring cohort. A combined analysis revealed significant independent validation of this association in both unrelated (p = 0.046) and family-based (p = 0.004) samples. The estimated risk conferred by this allele is small, and could easily be masked by small sample size, population stratification, or other confounders. These validation studies suggest that the original association is less likely to be spurious, but the failure to observe an association in every data set suggests that the effect of SNP rs7566605 on BMI may be heterogeneous across population samples.
机译:最近,Herbert和同事通过体重指数(BMI)测量,发现INSIG2基因上游的SNP rs7566605与肥胖有关。首先在来自Framingham心脏研究后代队列的923个相关个体的全基因组关联扫描中,对86,604个SNP的数据首次观察到BMI升高与次要等位基因纯合性之间的关联。在另外四个队列中复制了该关联,但在第五个队列中未看到该关联。为了进一步评估该关联的一般可重复性,我们在来自多个种族的八个人口的九个大型队列中对rs7566605进行了基因分型(总n = 16,969)。我们使用基于家庭,基于人群和病例对照的设计,在隐性模型下测试了此变量与BMI的关联。我们在五个队列中观察到显着(p <0.05)关联,但在其他三个队列中则未发现关联。在Framingham心脏研究后代队列中,来自不相关个体的纵向数据在整个检查周期中的关联证据强度存在差异。组合分析显示,在无关样品(p = 0.046)和基于家族样品(p = 0.004)中,该关联均得到了显着的独立验证。该等位基因所带来的估计风险很小,并且很容易被小样本量,人群分层或其他混杂因素所掩盖。这些验证研究表明,原始关联不太可能是虚假的,但是未能在每个数据集中观察到关联,表明SNP rs7566605对BMI的影响在人群样本中可能是异质的。

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