Slager S L, Schaid D J
Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
Am J Hum Genet. 2001 Jun;68(6):1457-62. doi: 10.1086/320608. Epub 2001 May 15.
Traditional case-control studies provide a powerful and efficient method for evaluation of association between candidate genes and disease. The sampling of cases from multiplex pedigrees, rather than from a catchment area, can increase the likelihood that genetic cases are selected. However, use of all the related cases without accounting for their biological relationship can increase the type I error rate of the statistical test. To overcome this problem, we present an analysis method that is used to compare genotype frequencies between cases and controls, according to a trend in proportions as the dosage of the risk allele increases. This method uses the appropriate variance to account for the correlated family data, thus maintaining the correct type I error rate. The magnitude of the association is estimated by the odds ratio, with the variance of the odds ratio also accounting for the correlated data. Our method makes efficient use of data collected from multiplex families and should prove useful for the analysis of candidate genes among families sampled for linkage studies. An application of our method, to family data from a prostate cancer study, is presented to illustrate the method's utility.
传统的病例对照研究为评估候选基因与疾病之间的关联提供了一种强大而有效的方法。从多个家系而非从一个集水区中选取病例,可以增加选择到遗传病例的可能性。然而,在不考虑病例之间生物学关系的情况下使用所有相关病例,会增加统计检验的I型错误率。为了克服这个问题,我们提出了一种分析方法,该方法用于根据风险等位基因剂量增加时比例的趋势,比较病例组和对照组之间的基因型频率。这种方法使用适当的方差来处理相关的家系数据,从而维持正确的I型错误率。关联的大小通过比值比来估计,比值比的方差也考虑了相关数据。我们的方法有效地利用了从多个家系收集的数据,并且应该被证明对在为连锁研究而抽样的家系中分析候选基因是有用的。本文展示了我们的方法在一项前列腺癌研究的家系数据中的应用,以说明该方法的实用性。