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多基因风险评分关联图谱,突出人类表型全范围的潜在因果关系。

An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome.

机构信息

MRC Integrative Epidemiology Unit (IEU), Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

出版信息

Elife. 2019 Mar 5;8:e43657. doi: 10.7554/eLife.43657.

Abstract

The age of large-scale genome-wide association studies (GWAS) has provided us with an unprecedented opportunity to evaluate the genetic liability of complex disease using polygenic risk scores (PRS). In this study, we have analysed 162 PRS (p<5×10) derived from GWAS and 551 heritable traits from the UK Biobank study (N = 334,398). Findings can be investigated using a web application (http:‌//‌mrcieu.‌mrsoftware.org/‌PRS‌_atlas/), which we envisage will help uncover both known and novel mechanisms which contribute towards disease susceptibility. To demonstrate this, we have investigated the results from a phenome-wide evaluation of schizophrenia genetic liability. Amongst findings were inverse associations with measures of cognitive function which extensive follow-up analyses using Mendelian randomization (MR) provided evidence of a causal relationship. We have also investigated the effect of multiple risk factors on disease using mediation and multivariable MR frameworks. Our atlas provides a resource for future endeavours seeking to unravel the causal determinants of complex disease.

摘要

大规模全基因组关联研究(GWAS)的时代为我们提供了一个前所未有的机会,利用多基因风险评分(PRS)评估复杂疾病的遗传易感性。在这项研究中,我们分析了来自英国生物库研究的 162 个 PRS(p<5×10)和 551 个可遗传特征(N=334398)。可以使用网络应用程序(http:‌//‌mrcieu.‌mrsoftware.org/‌PRS‌_atlas/)来研究这些发现,我们预计这将有助于揭示导致疾病易感性的已知和新的机制。为了证明这一点,我们对精神分裂症遗传易感性的全表型评估结果进行了研究。其中包括与认知功能测量值呈反比的关联,而孟德尔随机化(MR)的广泛后续分析提供了因果关系的证据。我们还使用中介和多变量 MR 框架研究了多种风险因素对疾病的影响。我们的图谱为未来旨在揭示复杂疾病因果决定因素的努力提供了资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4181/6400585/8e41aae0e8ca/elife-43657-fig1.jpg

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