Li Tengfei, Li Zhaohai, Ying Zhiliang, Zhang Hong
Department of Mathematics, Fudan University, 220 Handan Road, Shanghai 200433, PR China.
Ann Hum Genet. 2010 Jul;74(4):351-60. doi: 10.1111/j.1469-1809.2010.00588.x. Epub 2010 May 31.
Population-based genetic association analysis may suffer from the failure to control for confounders such as population stratification (PS). There has been extensive study on the influence of PS on candidate gene-disease association analysis, but much less attention has been paid to its influence on marker-disease association analysis. In this paper, we focus on the Pearson chi(2) test and the trend test for marker-disease association analysis. The mean and variance of the test statistics are derived under presence of PS, so that the power and inflated type I error rate can be evaluated. It is shown that the bias and the variance distortion are not zero in the presence of both PS and penetrance heterogeneity (PH). Unlike candidate gene-disease association analysis, when PS is present, the bias is not zero no matter whether PH is present or not. This work generalises the published results, where only the fully recessive penetrance model is considered and only the bias is calculated. It is shown that candidate gene-disease association analysis can be treated as a special case of marker-disease association analysis. Consequently, our results extend previous studies on candidate gene-disease association analysis. A simulation study confirms the theoretical findings.
基于人群的基因关联分析可能会因未能控制诸如人群分层(PS)等混杂因素而受到影响。关于PS对候选基因-疾病关联分析的影响已有广泛研究,但对其对标记物-疾病关联分析的影响关注较少。在本文中,我们聚焦于标记物-疾病关联分析的Pearson卡方检验和趋势检验。在存在PS的情况下推导了检验统计量的均值和方差,以便能够评估检验效能和膨胀的I型错误率。结果表明,在同时存在PS和外显率异质性(PH)的情况下,偏差和方差畸变不为零。与候选基因-疾病关联分析不同,当存在PS时,无论是否存在PH,偏差都不为零。这项工作推广了已发表的结果,其中仅考虑了完全隐性外显率模型且仅计算了偏差。结果表明,候选基因-疾病关联分析可被视为标记物-疾病关联分析的一个特例。因此,我们的结果扩展了先前关于候选基因-疾病关联分析的研究。一项模拟研究证实了理论发现。