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Stratification-Score Matching Improves Correction for Confounding by Population Stratification in Case-Control Association Studies

机译:病例-对照协会研究中的分层-得分匹配提高了人口分层对混杂因素的纠正

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摘要

Proper control of confounding due to population stratification is crucial for valid analysis of case-control association studies. Fine matching of cases and controls based on genetic ancestry is an increasingly popular strategy to correct for such confounding, both in genome-wide association studies (GWASs) as 'well as studies that employ next-generation sequencing, where matching can be used when selecting a subset of participants from a GWAS for rare-variant analysis. Existing matching methods match on measures of genetic ancestry that combine multiple components of ancestry into a scalar quantity. However, we show that including nonconfounding ancestry components in a matching criterion can lead to inaccurate matches, and hence to an improper control of confounding. To resolve this issue, we propose a novel method that assigns cases and controls to matched strata based on the stratification score (Epstein et al. [2007] Am } Hum Genet 80:921-930), which is the probability of disease given genomic variables. Matching on the stratification score leads to more accurate matches because case participants are matched to control participants who have a similar risk of disease given ancestry information. We illustrate our matching method using the African-American arm of the GAIN GWAS of schizophrenia. In this study, we observe that confounding due to stratification can be resolved by our matching approach but not by other existing matching procedures. We also use simulated data to show our novel matching approach can provide a more appropriate correction for population stratification than existing matching approaches.
机译:正确控制由于人口分层而造成的混淆,对于有效分析病例对照协会研究至关重要。基于基因组的病例和对照的精细匹配是纠正这种混淆的一种越来越流行的策略,在全基因组关联研究(GWAS)以及采用下一代测序的研究中都可以使用,在选择时可以使用匹配来自GWAS的参与者的子集,用于稀有变异分析。现有的匹配方法根据遗传祖先的度量进行匹配,该度量将祖先的多个组成部分组合为标量。但是,我们表明,在匹配标准中包含不混杂的祖先成分可能会导致不正确的匹配,从而导致对混杂的控制不当。为了解决这个问题,我们提出了一种新的方法,该方法根据分层得分将病例和对照分配给匹配的分层(Epstein等人,[2007] Am} Hum Genet 80:921-930),这是基因组导致疾病的可能性变量。在分层评分上进行匹配会导致更准确的匹配,因为根据祖先信息将案例参与者与具有相似疾病风险的对照参与者进行匹配。我们举例说明了使用精神分裂症患者GAIN GWAS的非洲裔美国人手臂进行匹配的方法。在这项研究中,我们观察到分层引起的混淆可以通过我们的匹配方法来解决,而不能通过其他现有的匹配程序来解决。我们还使用模拟数据表明,与现有匹配方法相比,我们新颖的匹配方法可以为人口分层提供更适当的校正。

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