Correcting Systematic Inflation in Genetic Association Tests That Consider Interaction Effects Application to a Genome-wide Association Study of Posttraumatic Stress Disorder

被引:40
作者
Almli, Lynn M. [1 ]
Duncan, Richard [2 ]
Feng, Hao [2 ]
Ghosh, Debashis [3 ]
Binder, Elisabeth B. [1 ,4 ]
Bradley, Bekh [1 ,5 ]
Ressler, Kerry J. [1 ]
Conneely, Karen N. [2 ]
Epstein, Michael P. [2 ]
机构
[1] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
[3] Penn State Univ, Dept Stat, State Coll, PA USA
[4] Max Planck Inst Psychiat, Dept Translat Res Psychiat, D-80804 Munich, Germany
[5] Dept Vet Affairs Med Ctr, Mental Hlth Serv Line, Atlanta, GA USA
关键词
SEROTONIN TRANSPORTER GENOTYPE; ENVIRONMENT INTERACTIONS; FEAR INHIBITION; TRAUMA EXPOSURE; RISK; PTSD; NEUROCIRCUITRY; VARIANTS; SYMPTOMS; RECEPTOR;
D O I
10.1001/jamapsychiatry.2014.1339
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
IMPORTANCE Genetic association studies of psychiatric outcomes often consider interactions with environmental exposures and, in particular, apply tests that jointly consider gene and gene-environment interaction effects for analysis. Using a genome-wide association study (GWAS) of posttraumatic stress disorder (PTSD), we report that heteroscedasticity (defined as variability in outcome that differs by the value of the environmental exposure) can invalidate traditional joint tests of gene and gene-environment interaction. OBJECTIVES To identify the cause of bias in traditional joint tests of gene and gene-environment interaction in a PTSD GWAS and determine whether proposed robust joint tests are insensitive to this problem. DESIGN, SETTING, AND PARTICIPANTS The PTSD GWAS data set consisted of 3359 individuals (978 men and 2381 women) from the Grady Trauma Project (GTP), a cohort study from Atlanta, Georgia. The GTP performed genome-wide genotyping of participants and collected environmental exposures using the Childhood Trauma Questionnaire and Trauma Experiences Inventory. MAIN OUTCOMES AND MEASURES We performed joint interaction testing of the Beck Depression Inventory and modified PTSD Symptom Scale in the GTP GWAS. We assessed systematic bias in our interaction analyses using quantile-quantile plots and genome-wide inflation factors. RESULTS Application of the traditional joint interaction test to the GTP GWAS yielded systematic inflation across different outcomes and environmental exposures (inflation-factor estimates ranging from 1.07 to 1.21), whereas application of the robust joint test to the same data set yielded no such inflation (inflation-factor estimates ranging from 1.01 to 1.02). Simulated data further revealed that the robust joint test is valid in different heteroscedasticity models, whereas the traditional joint test is invalid. The robust joint test also has power similar to the traditional joint test when heteroscedasticity is not an issue. CONCLUSIONS AND RELEVANCE We believe the robust joint test should be used in candidate-gene studies and GWASs of psychiatric outcomes that consider environmental interactions. To make the procedure useful for applied investigators, we created a software tool that can be called from the popular PLINK package for analysis.
引用
收藏
页码:1392 / 1399
页数:8
相关论文
共 57 条
[1]
[Anonymous], 1998, Manual for the childhood trauma questionnaire
[2]
[Anonymous], ECONOMETRIC ANAL
[3]
Genome-Wide Meta-Analysis of Joint Tests for Genetic and Gene-Environment Interaction Effects [J].
Aschard, Hugues ;
Hancock, Dana B. ;
London, Stephanie J. ;
Kraft, Peter .
HUMAN HEREDITY, 2010, 70 (04) :292-300
[4]
ProbABEL package for genome-wide association analysis of imputed data [J].
Aulchenko, Yurii S. ;
Struchalin, Maksim V. ;
van Duijn, Cornelia M. .
BMC BIOINFORMATICS, 2010, 11
[5]
AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[6]
Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults [J].
Binder, Elisabeth B. ;
Bradley, Rebekah G. ;
Liu, Wei ;
Epstein, Michael P. ;
Deveau, Todd C. ;
Mercer, Kristina B. ;
Tang, Yilang ;
Gillespie, Charles F. ;
Heim, Christine M. ;
Nemeroff, Charles B. ;
Schwartz, Ann C. ;
Cubells, Joseph F. ;
Ressler, Kerry J. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 299 (11) :1291-1305
[7]
Breslau N, 2001, J CLIN PSYCHIAT, V62, P16
[8]
ROBUST TESTS FOR EQUALITY OF VARIANCES [J].
BROWN, MB ;
FORSYTHE, AB .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1974, 69 (346) :364-367
[9]
Serniparametric maximum likelihood estimation exploiting gene-environment independence in case-control studies [J].
Chatterjee, N ;
Carroll, RJ .
BIOMETRIKA, 2005, 92 (02) :399-418
[10]
Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions [J].
Chatterjee, Nilanjan ;
Kalaylioglu, Zeynep ;
Moslehi, Roxana ;
Peters, Ulrike ;
Wacholder, Sholom .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 79 (06) :1002-1016