TY - JOUR
T1 - Posttraumatic stress disorder; combat exposure; and nicotine dependence, alcohol dependence, and major depression in male twins
AU - Scherrer, Jeffrey F.
AU - Xian, Hong
AU - Lyons, Michael J.
AU - Goldberg, Jack
AU - Eisen, Seth A.
AU - True, William R.
AU - Tsuang, Ming
AU - Bucholz, Kathleen K.
AU - Koenen, Karestan C.
N1 - Funding Information:
This work was supported by National Institutes of Health grants AA12640, AA11667, AA11998, DA14363, and DA020810. Dr Koenen is supported in part by MH070627. Additional funding was provided by the National Institute on Drug Abuse and the Robert Wood Johnson Foundation. The US Department of Veterans Affairs has provided financial support for the development and maintenance of the VET Registry. Numerous organizations have provided invaluable assistance in the conduct of this study, including the Department of Defense; the National Personnel Records Center, National Archives and Records Administration; the Internal Revenue Service; the National Opinion Research Center; the National Research Council, National Academy of Sciences; and the Institute for Survey Research, Temple University. Most importantly, the authors gratefully acknowledge the continued cooperation and participation of the members of the VET Registry and their families. Without their contribution, this research would not have been possible. Drs Scherrer and Xian had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
PY - 2008/5
Y1 - 2008/5
N2 - Combat exposure is associated with increased risk of psychiatric and substance use disorders in veterans. However, it is not known whether combat exposure independently increases risk for these disorders or whether this association is accounted for by genetic vulnerability common to posttraumatic stress disorder (PTSD). This article tests competing explanations for the association of combat exposure and PTSD with nicotine dependence (ND), alcohol dependence (AD), and major depression (MD). Data were obtained from 6099 members of the Vietnam Era Twin Registry, a national registry of male-male twin pairs who served in the military during the Vietnam era. Twin models were fit to estimate the genetic and environmental variance common and specific to Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition, lifetime diagnoses of PTSD, combat trauma, and 3 comorbid conditions: ND, AD, and MD. Variance specific to ND, AD, and MD was due to genetic factors (48%, 36%, and 12%, respectively) and unique environmental factors (36%, 42%, and 58%, respectively). After accounting for variance common to PTSD, no residual genetic and environmental variance overlapped between combat and ND, combat and AD, and combat and MD. Combat exposure is not independently associated with lifetime ND, AD, and MD. The association of combat exposure with these 3 disorders is due to genetic and unique environmental contributions in common with PTSD. These findings suggest comorbid PTSD may represent a genetically mediated vulnerability to psychopathology after trauma.
AB - Combat exposure is associated with increased risk of psychiatric and substance use disorders in veterans. However, it is not known whether combat exposure independently increases risk for these disorders or whether this association is accounted for by genetic vulnerability common to posttraumatic stress disorder (PTSD). This article tests competing explanations for the association of combat exposure and PTSD with nicotine dependence (ND), alcohol dependence (AD), and major depression (MD). Data were obtained from 6099 members of the Vietnam Era Twin Registry, a national registry of male-male twin pairs who served in the military during the Vietnam era. Twin models were fit to estimate the genetic and environmental variance common and specific to Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition, lifetime diagnoses of PTSD, combat trauma, and 3 comorbid conditions: ND, AD, and MD. Variance specific to ND, AD, and MD was due to genetic factors (48%, 36%, and 12%, respectively) and unique environmental factors (36%, 42%, and 58%, respectively). After accounting for variance common to PTSD, no residual genetic and environmental variance overlapped between combat and ND, combat and AD, and combat and MD. Combat exposure is not independently associated with lifetime ND, AD, and MD. The association of combat exposure with these 3 disorders is due to genetic and unique environmental contributions in common with PTSD. These findings suggest comorbid PTSD may represent a genetically mediated vulnerability to psychopathology after trauma.
UR - http://www.scopus.com/inward/record.url?scp=41549087940&partnerID=8YFLogxK
U2 - 10.1016/j.comppsych.2007.11.001
DO - 10.1016/j.comppsych.2007.11.001
M3 - Article
C2 - 18396190
AN - SCOPUS:41549087940
SN - 0010-440X
VL - 49
SP - 297
EP - 304
JO - Comprehensive Psychiatry
JF - Comprehensive Psychiatry
IS - 3
ER -