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一种用于病例-父母-三联体数据的对数线性方法:评估直接起作用或通过母体效应起作用且可能受到亲本印记影响的疾病基因的效应。

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.

作者信息

Weinberg C R, Wilcox A J, Lie R T

机构信息

Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Am J Hum Genet. 1998 Apr;62(4):969-78. doi: 10.1086/301802.

Abstract

We describe a log-linear method for analysis of case-parent-triad data, based on maximum likelihood with stratification on parental mating type. The method leads to estimates of association parameters, such as relative risks, for a single allele, and also to likelihood ratio chi2 tests (LRTs) of linkage disequilibrium. Hardy-Weinberg equilibrium need not be assumed. Our simulations suggest that the LRT has power similar to that of the chi2 "score" test proposed by Schaid and Sommer and that both can outperform the transmission/disequilibrium test (TDT), although the TDT can perform better under an additive model of inheritance. Because a restricted version of the LRT is asymptotically equivalent to the TDT, the proposed test can be regarded as a generalization of the TDT. The method that we describe generalizes easily to accommodate maternal effects on risk and, in fact, produces powerful and orthogonal tests of the contribution of fetal versus maternal genetic factors. We further generalize the model to allow for effects of parental imprinting. Imprinting effects can be fitted by a simple, iterative procedure that relies on the expectation-maximization algorithm and that uses standard statistical software for the maximization steps. Simulations reveal that LRT tests for detection of imprinting have very good operating characteristics. When a single allele is under study, the proposed method can yield powerful tests for detection of linkage disequilibrium and is applicable to a broader array of causal scenarios than is the TDT.

摘要

我们描述了一种用于分析病例-双亲三联体数据的对数线性方法,该方法基于最大似然法,并按亲代交配类型进行分层。该方法可得出单个等位基因关联参数(如相对风险)的估计值,还可进行连锁不平衡的似然比卡方检验(LRT)。无需假定哈迪-温伯格平衡。我们的模拟表明,LRT的效能与Schaid和Sommer提出的卡方“计分”检验相似,并且两者都可能优于传递/不平衡检验(TDT),尽管在加性遗传模型下TDT可能表现更好。由于LRT的一个受限版本与TDT渐近等效,因此所提出的检验可被视为TDT的推广。我们描述的方法很容易推广以适应母体对风险的影响,实际上,它能对胎儿与母体遗传因素的贡献进行效能强大且相互独立的检验。我们进一步推广该模型以考虑亲代印记效应。印记效应可以通过一个简单的迭代程序来拟合,该程序依赖于期望最大化算法,并在最大化步骤中使用标准统计软件。模拟结果表明,用于检测印记的LRT检验具有非常好的操作特性。当研究单个等位基因时,所提出的方法可产生用于检测连锁不平衡的效能强大的检验,并且比TDT适用于更广泛的因果情形。

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