Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH, USA.
Hum Genomics. 2009 Oct;4(1):2-20. doi: 10.1186/1479-7364-4-1-2.
With the trend in molecular epidemiology towards both genome-wide association studies and complex modelling, the need for large sample sizes to detect small effects and to allow for the estimation of many parameters within a model continues to increase. Unfortunately, most methods of association analysis have been restricted to either a family-based or a case-control design, resulting in the lack of synthesis of data from multiple studies. Transmission disequilibrium-type methods for detecting linkage disequilibrium from family data were developed as an effective way of preventing the detection of association due to population stratification. Because these methods condition on parental genotype, however, they have precluded the joint analysis of family and case-control data, although methods for case-control data may not protect against population stratification and do not allow for familial correlations. We present here an extension of a family-based association analysis method for continuous traits that will simultaneously test for, and if necessary control for, population stratification. We further extend this method to analyse binary traits (and therefore family and case-control data together) and accurately to estimate genetic effects in the population, even when using an ascertained family sample. Finally, we present the power of this binary extension for both family-only and joint family and case-control data, and demonstrate the accuracy of the association parameter and variance components in an ascertained family sample.
随着分子流行病学向全基因组关联研究和复杂模型的发展,检测小效应和在模型中估计许多参数的需要继续增加,这就需要大量的样本量。不幸的是,大多数关联分析方法都仅限于基于家庭或病例对照的设计,从而导致缺乏对多个研究数据的综合。为了防止由于群体分层而导致关联的检测,从家族数据中检测连锁不平衡的传递不平衡型方法被开发为一种有效的方法。然而,由于这些方法取决于父母的基因型,因此它们排除了家族和病例对照数据的联合分析,尽管病例对照数据的方法可能无法防止群体分层,也不允许家族相关性。我们在这里提出了一种连续性状的基于家族的关联分析方法的扩展,该方法将同时检测并在必要时控制群体分层。我们进一步将这种方法扩展到分析二项性状(因此同时分析家族和病例对照数据),并在使用已确定的家族样本时准确估计人群中的遗传效应。最后,我们展示了这种二进制扩展对于仅家族和联合家族和病例对照数据的功效,并证明了在已确定的家族样本中关联参数和方差分量的准确性。