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Adjustment for index event bias in genome-wide association studies of subsequent events

机译:在后续事件的全基因组关联研究中对索引事件偏倚的调整

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摘要

Following numerous genome-wide association studies of disease susceptibility, there is increasing interest in genetic associations with prognosis, survival or other subsequent events. Such associations are vulnerable to index event bias, by which selection of subjects according to disease status creates biased associations if common causes of incidence and prognosis are not accounted for. We propose an adjustment for index event bias using the residuals from the regression of genetic effects on prognosis on genetic effects on incidence. Our approach eliminates this bias when direct genetic effects on incidence and prognosis are independent, and otherwise reduces bias in realistic situations. In a study of idiopathic pulmonary fibrosis, we reverse a paradoxical association of the strong susceptibility gene MUC5B with increased survival, suggesting instead a significant association with decreased survival. In re-analysis of a study of Crohn’s disease prognosis, four regions remain associated at genome-wide significance but with increased standard errors.
机译:在对疾病易感性的全基因组关联研究之后,人们对与预后,生存或其他后续事件的遗传关联越来越感兴趣。这样的关联很容易受到索引事件偏倚的影响,如果不考虑常见的发病原因和预后,则根据疾病状况选择受试者会产生偏倚的关联。我们提出了一种对指数事件偏倚的调整,该调整使用了遗传效应对预后的回归对遗传影响的发生率的残差。当对发生率和预后的直接遗传影响是独立的时,我们的方法消除了这种偏见,并且在现实情况下减少了偏见。在一项特发性肺纤维化的研究中,我们逆转了强易感性基因MUC5B与存活率增加之间的自相矛盾的关联,提示与降低的存活率存在显着关联。在重新分析克罗恩氏病预后的研究中,四个区域在全基因组意义上仍具有相关性,但标准误增加。

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