Schwender Holger, Taub Margaret A, Beaty Terri H, Marazita Mary L, Ruczinski Ingo
TU Dortmund University, 44221 Dortmund, Germany.
Biometrics. 2012 Sep;68(3):766-73. doi: 10.1111/j.1541-0420.2011.01713.x. Epub 2011 Dec 7.
Case-parent trio studies concerned with children affected by a disease and their parents aim to detect single nucleotide polymorphisms (SNPs) showing a preferential transmission of alleles from the parents to their affected offspring. A popular statistical test for detecting such SNPs associated with disease in this study design is the genotypic transmission/disequilibrium test (gTDT) based on a conditional logistic regression model, which usually needs to be fitted by an iterative procedure. In this article, we derive exact closed-form solutions for the parameter estimates of the conditional logistic regression models when testing for an additive, a dominant, or a recessive effect of a SNP, and show that such analytic parameter estimates also exist when considering gene-environment interactions with binary environmental variables. Because the genetic model underlying the association between a SNP and a disease is typically unknown, it might further be beneficial to use the maximum over the gTDT statistics for the possible effects of a SNP as test statistic. We therefore propose a procedure enabling a fast computation of the test statistic and the permutation-based p-value of this MAX gTDT. All these methods are applied to whole-genome scans of the case-parent trios from the International Cleft Consortium. These applications show our procedures dramatically reduce the required computing time compared to the conventional iterative methods allowing, for example, the analysis of hundreds of thousands of SNPs in a few minutes instead of several hours.
病例-双亲三联体研究关注受疾病影响的儿童及其父母,旨在检测单核苷酸多态性(SNP),这些多态性显示出等位基因从父母向其患病后代的优先传递。在该研究设计中,用于检测此类与疾病相关的SNP的一种常用统计检验是基于条件逻辑回归模型的基因型传递/不平衡检验(gTDT),该模型通常需要通过迭代程序进行拟合。在本文中,我们推导了在检验SNP的加性、显性或隐性效应时条件逻辑回归模型参数估计的精确闭式解,并表明在考虑与二元环境变量的基因-环境相互作用时也存在此类解析参数估计。由于SNP与疾病之间关联的潜在遗传模型通常未知,将SNP可能效应的gTDT统计量的最大值用作检验统计量可能会更有益。因此,我们提出了一种程序,能够快速计算该MAX gTDT的检验统计量和基于置换的p值。所有这些方法都应用于国际腭裂联盟病例-双亲三联体的全基因组扫描。这些应用表明,与传统的迭代方法相比,我们的程序显著减少了所需的计算时间,例如,可以在几分钟内而不是几小时内分析数十万SNP。