Invited Commentary: Efficient Testing of Gene-Environment Interaction

被引:15
作者
Chatterjee, Nilanjan [1 ]
Wacholder, Sholom [1 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
关键词
DESIGNS;
D O I
10.1093/aje/kwn352
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Gene-environment-wide interaction studies of disease occurrence in human populations may be able to exploit the same agnostic approach to interrogating the human genome used by genome-wide association studies. The authors discuss 2 methods for taking advantage of possible independence between a single nucleotide polymorphism they call G (a genetic factor) and an environmental factor they call E while maintaining nominal type I error in studying G-E interaction when information on many genes is available. The first method is a simple 2-step procedure for testing the null hypothesis of no multiplicative interaction against the alternative hypothesis of a multiplicative interaction between an E and at least one of the markers genotyped in a genome-wide association study. The added power for the method derives from a clever work-around of a multiple testing procedure. The second is an empirical-Bayes-style shrinkage estimation framework for G-E interaction and the associated tests that can gain efficiency and power when the G-E independence assumption is met for most G's in the underlying population and yet, unlike the case-only method, is resistant to increased type I error when the underlying assumption of independence is violated. The development of new approaches to testing for interaction is an example of methodological progress leading to practical advantages.
引用
收藏
页码:231 / 233
页数:3
相关论文
共 10 条
[1]   Limitations of the case-only design for identifying gene-environment interactions [J].
Albert, PS ;
Ratnasinghe, D ;
Tangrea, J ;
Wacholder, S .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2001, 154 (08) :687-693
[2]   Invited Commentary: From Genome-Wide Association Studies to Gene-Environment-Wide Interaction Studies-025EFChallenges and Opportunities [J].
Khoury, Muin J. ;
Wacholder, Sholom .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2009, 169 (02) :227-230
[3]   Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation [J].
Modan, B ;
Hartge, P ;
Hirsh-Yechezkel, G ;
Chetrit, A ;
Lubin, F ;
Beller, U ;
Ben-Baruch, G ;
Fishman, A ;
Menczer, J ;
Struewing, JP ;
Tucker, MA ;
Wacholder, S ;
Ebbers, SM ;
Friedman, E ;
Piura, B .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (04) :235-240
[4]   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
[5]   Tests for Gene-Environment Interaction From Case-Control Data: A Novel Study of Type I Error, Power and Designs [J].
Mukherjee, Bhramar ;
Ahn, Jaeil ;
Gruber, Stephen B. ;
Rennert, Gad ;
Moren, Victor ;
Chatterjee, Nilanjan .
GENETIC EPIDEMIOLOGY, 2008, 32 (07) :615-626
[6]   Gene-Environment Interaction in Genome-Wide Association Studies [J].
Murcray, Cassandra E. ;
Lewinger, Juan Pablo ;
Gauderman, W. James .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2009, 169 (02) :219-226
[7]   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
[8]   Clustered environments and randomized genes: A fundamental distinction between conventional and genetic epidemiology [J].
Smith, George Davey ;
Lawlor, Debbie A. ;
Harbord, Roger ;
Timpson, Nic ;
Day, Ian ;
Ebrahim, Shah .
PLOS MEDICINE, 2007, 4 (12) :1985-1992
[9]   Analysis of case-control studies of genetic and environmental factors with missing genetic information and haplotype-phase ambiguity [J].
Spinka, C ;
Carroll, RJ ;
Chatterjee, N .
GENETIC EPIDEMIOLOGY, 2005, 29 (02) :108-127
[10]   Assessing the probability that a positive report is false: An approach for molecular epidemiology studies [J].
Wacholder, S ;
Chanock, S ;
Garcia-Closas, M ;
El ghormli, L ;
Rothman, N .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (06) :434-442