Meta-analysis of genetic association studies under heterogeneity

被引:10
|
作者
Neupane, Binod [1 ]
Loeb, Mark [1 ,2 ]
Anand, Sonia S. [1 ]
Beyene, Joseph [1 ]
机构
[1] McMaster Univ, Populat Genom Program, Dept Clin Epidemiol & Biostat, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
genome-wide and genetic association studies; single-nucleotide polymorphism; meta-analysis; study heterogeneity; statistical power; type I error rates; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; RISK; INCONSISTENCY; REPLICATION; VARIANTS;
D O I
10.1038/ejhg.2012.75
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In multi-cohort genetic association studies or meta-analysis, associations of genetic variants with complex traits across cohorts may be heterogeneous because of genuine genetic diversity or differential biases or errors. To detect the associations of genes with heterogeneous associations across cohorts, new global fixed-effect (FE) and random-effects (RE) meta-analytic methods have been recently proposed. These global methods had improved power over both traditional FE and RE methods under heterogeneity in limited simulation scenarios and data application, but their usefulness in a wide range of practical situations is not clear. We assessed the performance of these methods for both binary and quantitative traits in extensive simulations and applied them to a multi-cohort association study. We found that these new approaches have higher power to detect mostly the very small to small associations of common genetic variants when associations are highly heterogeneous across cohorts. They worked well when both the underlying and assumed genetic models are either multiplicative or dominant. But, they offered no clear advantage for less common variants unless heterogeneity was substantial. In conclusion, these new meta-analytic methods can be used to detect the association of genetic variants with high heterogeneity, which can then be subjected to further exploration, in multi-cohort association studies and meta-analyses. European Journal of Human Genetics (2012) 20, 1174-1181; doi: 10.1038/ejhg.2012.75; published online 30 May 2012
引用
收藏
页码:1174 / 1181
页数:8
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