Beyene Joseph, Hamid Jemila S
Department of Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, ON, Canada; Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, ON, Canada.
Genet Epidemiol. 2014 Sep;38 Suppl 1:S68-73. doi: 10.1002/gepi.21828.
Genome-wide association studies have led to the discovery of thousands of susceptibility genetic variants (typically single-nucleotide polymorphisms [SNPs]) for a wide range of complex diseases and traits commonly measured at a single point in time. Although many novel genotype-phenotype associations have been identified and successfully replicated using cross-sectionally measured phenotypes, there is growing interest in the study of longitudinally measured phenotypes because these allow for the study of the natural trajectory of traits and disease progression. However, there are several challenges with analysis and interpretation of longitudinal data. Here, we summarize the methods and strategies proposed and applied in genome-wide association studies of blood pressure related phenotypes made available through Genetic Analysis Workshop 18 (GAW18). The investigators considered methods that incorporated correlation across time points and familial relatedness among the individuals into their studies and compared their approaches with single-time-point analysis using baseline data. Some of the studies used unrelated individuals; some also used the simulated data provided by the GAW18 organizers to assess type I error and power of their approach in detecting true associations.
全基因组关联研究已促使人们发现了数千种与广泛的复杂疾病和性状相关的易感基因变异(通常为单核苷酸多态性[SNP]),这些疾病和性状通常在某一时刻进行测量。尽管已通过横断面测量的表型鉴定出许多新的基因型-表型关联并成功进行了复制,但对纵向测量表型的研究兴趣日益浓厚,因为这些表型有助于研究性状的自然轨迹和疾病进展。然而,纵向数据分析和解释存在若干挑战。在此,我们总结了在通过遗传分析研讨会18(GAW18)提供的血压相关表型的全基因组关联研究中提出并应用的方法和策略。研究人员在研究中考虑了将时间点之间的相关性以及个体之间的家族相关性纳入其中的方法,并将他们的方法与使用基线数据的单时间点分析进行了比较。一些研究使用了无亲缘关系的个体;一些研究还使用了GAW18组织者提供的模拟数据来评估其方法在检测真实关联中的I型错误和效能。