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Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia

机译:精神分裂症的多基因风险分数与祖先相关的精神分裂症与精神分裂症更强烈

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BackgroundThe polygenic risk score (PRS) for schizophrenia, derived from very large numbers of weakly associated genetic markers, has been repeatedly shown to be robustly associated with schizophrenia in independent samples and also with other diseases and traits.AimThis study aims to explore the distribution of the schizophrenia PRS in subjects of different ancestry.MethodsThe schizophrenia PRS derived from the large genome-wide association study carried out by the Psychiatric Genetics Consortium was calculated using the downloaded genotypes of HapMap subjects from 11 different ancestral groups. It was also calculated using downloaded genotypes of European schizophrenia cases and controls from the CommonMind Consortium.ResultsThe PRS for schizophrenia varied significantly between ancestral groups (P2x10(-16)) and was much higher in African than European HapMap subjects. The mean difference between these groups was 10 times as high as the mean difference between European schizophrenia cases and controls. The distributions of scores for African and European subjects hardly overlapped.ConclusionThe PRS cannot be regarded as simply a measure of the polygenic contribution to risk of schizophrenia and clearly contains a strong ancestry component. It is possible that this could be controlled to some extent by incorporating principal components as covariates, but doubts remain as to how it should be interpreted. The PRS derived from European subjects cannot be applied to non-Europeans, limiting its potential usefulness in clinical settings and raising issues of inequity in health provision. Previous studies that have used the PRS should be re-examined in the light of these findings.
机译:背景技术从非常大量的弱相关的遗传标记中衍生的精神分裂症的多基因风险评分(PRS)已经被反复显示与独立样品中的精神分裂症以及其他疾病和特质的精神分裂症稳健相关.IMAIMTHIS研究旨在探索分配来自不同祖先的科目的精神分裂症..使用来自11种不同的祖先群的Hapmap受试者的下载基因型来计算来自精神病遗传学联盟的大型基因组关联研究的精神分裂症PRS。它还使用欧洲精神分裂症病例的下载基因型来计算,并从Commonmind Consortium的控制。祖先群体之间的精神分裂症的PRS有显着变化(P <2×10(-16)),而非洲的比欧洲HAPMAP受试者要高得多。这些基团之间的平均差异是欧洲精神分裂症病例和对照的平均差异的10倍。非洲和欧洲受试者的分数几乎没有重叠。结论PRS不能被视为仅仅是对精神分裂症风险的衡量标准,并且显然含有强大的祖先组成部分。这可以通过将主要成分作为协变量纳入一定程度的方式来控制,但疑虑仍然是如何解释的。源自欧洲科目的PRS不能适用于非欧洲人,限制其在临床环境中的潜在有用性,并在卫生条款中提高不公平问题。应该根据这些发现重新检查使用该PRS的先前研究。

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