Improved Statistics for Genome-Wide Interaction Analysis

被引:71
作者
Ueki, Masao [1 ,2 ]
Cordell, Heather J. [2 ]
机构
[1] Yamagata Univ, Fac Med, Yamagata 990, Japan
[2] Newcastle Univ, Inst Med Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
来源
PLOS GENETICS | 2012年 / 8卷 / 04期
基金
英国惠康基金;
关键词
GENE-ENVIRONMENT INDEPENDENCE; SUSCEPTIBILITY LOCI; LINKAGE-DISEQUILIBRIUM; SAMPLE-SIZE; COMMON SNPS; ASSOCIATION; DISEASES; DETECT; HERITABILITY; EPISTASIS;
D O I
10.1371/journal.pgen.1002625
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recently, Wu and colleagues [1] proposed two novel statistics for genome-wide interaction analysis using case/control or case-only data. In computer simulations, their proposed case/control statistic outperformed competing approaches, including the fast-epistasis option in PLINK and logistic regression analysis under the correct model; however, reasons for its superior performance were not fully explored. Here we investigate the theoretical properties and performance of Wu et al.'s proposed statistics and explain why, in some circumstances, they outperform competing approaches. Unfortunately, we find minor errors in the formulae for their statistics, resulting in tests that have higher than nominal type 1 error. We also find minor errors in PLINK's fast-epistasis and case-only statistics, although theory and simulations suggest that these errors have only negligible effect on type 1 error. We propose adjusted versions of all four statistics that, both theoretically and in computer simulations, maintain correct type 1 error rates under the null hypothesis. We also investigate statistics based on correlation coefficients that maintain similar control of type 1 error. Although designed to test specifically for interaction, we show that some of these previously-proposed statistics can, in fact, be sensitive to main effects at one or both loci, particularly in the presence of linkage disequilibrium. We propose two new "joint effects" statistics that, provided the disease is rare, are sensitive only to genuine interaction effects. In computer simulations we find, in most situations considered, that highest power is achieved by analysis under the correct genetic model. Such an analysis is unachievable in practice, as we do not know this model. However, generally high power over a wide range of scenarios is exhibited by our joint effects and adjusted Wu statistics. We recommend use of these alternative or adjusted statistics and urge caution when using Wu et al.'s originally-proposed statistics, on account of the inflated error rate that can result.
引用
收藏
页码:141 / 159
页数:19
相关论文
共 38 条
[21]   Exploiting gene-environment independence for analysis of case-control studies: An empirical bayes-type shrinkage estimator to trade-off between bias and efficiency [J].
Mukherjee, Bhramar ;
Chatterjee, Nilanjan .
BIOMETRICS, 2008, 64 (03) :685-694
[22]   Epistasis - the essential role of gene interactions in the structure and evolution of genetic systems [J].
Phillips, Patrick C. .
NATURE REVIEWS GENETICS, 2008, 9 (11) :855-867
[23]  
Phillips PC, 1998, GENETICS, V149, P1167
[24]   NON-HIERARCHICAL LOGISTIC-MODELS AND CASE-ONLY DESIGNS FOR ASSESSING SUSCEPTIBILITY IN POPULATION-BASED CASE-CONTROL STUDIES [J].
PIEGORSCH, WW ;
WEINBERG, CR ;
TAYLOR, JA .
STATISTICS IN MEDICINE, 1994, 13 (02) :153-162
[25]   PLINK: A tool set for whole-genome association and population-based linkage analyses [J].
Purcell, Shaun ;
Neale, Benjamin ;
Todd-Brown, Kathe ;
Thomas, Lori ;
Ferreira, Manuel A. R. ;
Bender, David ;
Maller, Julian ;
Sklar, Pamela ;
de Bakker, Paul I. W. ;
Daly, Mark J. ;
Sham, Pak C. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (03) :559-575
[26]   From genotypes to genes: Doubling the sample size [J].
Sasieni, PD .
BIOMETRICS, 1997, 53 (04) :1253-1261
[27]   BIOLOGICAL MODELS AND STATISTICAL INTERACTIONS - AN EXAMPLE FROM MULTISTAGE CARCINOGENESIS [J].
SIEMIATYCKI, J ;
THOMAS, DC .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1981, 10 (04) :383-387
[28]   EFFECT MODIFICATION AND THE LIMITS OF BIOLOGICAL INFERENCE FROM EPIDEMIOLOGIC DATA [J].
THOMPSON, WD .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1991, 44 (03) :221-232
[29]   Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes [J].
Todd, John A. ;
Walker, Neil M. ;
Cooper, Jason D. ;
Smyth, Deborah J. ;
Downes, Kate ;
Plagnol, Vincent ;
Bailey, Rebecca ;
Nejentsev, Sergey ;
Field, Sarah F. ;
Payne, Felicity ;
Lowe, Christopher E. ;
Szeszko, Jeffrey S. ;
Hafler, Jason P. ;
Zeitels, Lauren ;
Yang, Jennie H. M. ;
Vella, Adrian ;
Nutland, Sarah ;
Stevens, Helen E. ;
Schuilenburg, Helen ;
Coleman, Gillian ;
Maisuria, Meeta ;
Meadows, William ;
Smink, Luc J. ;
Healy, Barry ;
Burren, Oliver S. ;
Lam, Alex A. C. ;
Ovington, Nigel R. ;
Allen, James ;
Adlem, Ellen ;
Leung, Hin-Tak ;
Wallace, Chris ;
Howson, Joanna M. M. ;
Guja, Cristian ;
Ionescu-Tirgoviste, Constantin ;
Simmonds, Matthew J. ;
Heward, Joanne M. ;
Gough, Stephen C. L. ;
Dunger, David B. ;
Wicker, Linda S. ;
Clayton, David G. .
NATURE GENETICS, 2007, 39 (07) :857-864
[30]   The Meaning of Interaction [J].
Wang, Xuefeng ;
Elston, Robert C. ;
Zhu, Xiaofeng .
HUMAN HEREDITY, 2010, 70 (04) :269-277