TY - JOUR
T1 - Population admixture modulates risk for alcohol dependence
AU - Zuo, Lingjun
AU - Luo, Xingguang
AU - Listman, Jennifer B.
AU - Kranzler, Henry R.
AU - Wang, Shuang
AU - Anton, Raymond F.
AU - Blumberg, Hilary P.
AU - Stein, Murray B.
AU - Pearlson, Godfrey D.
AU - Covault, Jonathan
AU - Charney, Dennis S.
AU - van Kammen, Daniel P.
AU - Price, Lawrence H.
AU - Lappalainen, Jaakko
AU - Cramer, Joyce
AU - Krystal, John H.
AU - Gelernter, Joel
N1 - Funding Information:
McKain, Michelle Slivinsky, Konstantin Voronin and Carolyn Wenner assisted with patient interviews. This work was supported in part by National Institute on Drug Abuse (NIDA) grants R01-DA12849, R01-DA12690, K24-DA15105, and DA020709, National Institute on Alcohol Abuse and Alcoholism (NIAAA) grants R01-AA11330, R01-AA016015, P50-AA12870, P50-AA03510, K24-AA13736, R01-AA015615 and K05-AA14906, National Institute on Mental Health grants R01-MH43775 and R01-MH70902, National Center for Research Resources (NCRR) grant M01-RR06192, Alcoholic Beverage Medical Research Foundation (ABMRF) grant award R06932 (X. Luo); and by the U.S. Department of Veterans AVairs (the VA Alcohol Research Center, the VA Medical Research Program, the VA Connecticut–Massachusetts Mental Illness Research, Education and Clinical Center [MIRECC], and the VA Research Enhancement Award Program [REAP] research center). Drs. Mark D. Shriver and Robert Rosenheck provided some of the DNA samples. We thank the Department of Veterans AVairs Cooperative Study Group on Clozapine in Refractory Schizophrenia (members of the study group are listed in Rosenheck et al. (1997) and some investigators from Project MATCH, a collaborative clinical trial sponsored by NIAAA, who provided phenotypic data and blood samples for DNA extraction and genotyping.
PY - 2009
Y1 - 2009
N2 - The admixture of different ancestral populations in America may have important implications for the risk for psychiatric disorders, as it appears to have for other medical disorders. The present study investigated the role of population admixture in risk for several psychiatric disorders in European-Americans (EAs) and African-Americans (AAs). This is a multisite study with 3,792 subjects recruited from across the United States, including 3,119 EAs and 673 AAs. These subjects included healthy controls and those with substance dependence (SD) [including alcohol dependence (AD), cocaine dependence, and opioid dependence], social phobia, affective disorders, and schizophrenia. In addition, DNA was included from 78 West Africans. The degree of admixture for each subject was estimated by analysis of a set of ancestry-informative genetic markers using the program STRUCTURE, and was compared between cases and controls. As noted previously, the degree of admixture in AAs was higher than EAs. In EAs, the degree of admixture (with African ancestry) was significantly lower in patients with SD (mainly AD) than controls (P = 0.009 for SD; P = 0.008 for AD). This finding suggests that population admixture may modulate risk for alcohol dependence. Population admixture might protect against alcohol dependence by increasing average heterozygosity and reducing the risk of deleterious recessive alleles. We cannot exclude the possibility that the results might have been influenced by selection bias due to the multisite nature of the study.
AB - The admixture of different ancestral populations in America may have important implications for the risk for psychiatric disorders, as it appears to have for other medical disorders. The present study investigated the role of population admixture in risk for several psychiatric disorders in European-Americans (EAs) and African-Americans (AAs). This is a multisite study with 3,792 subjects recruited from across the United States, including 3,119 EAs and 673 AAs. These subjects included healthy controls and those with substance dependence (SD) [including alcohol dependence (AD), cocaine dependence, and opioid dependence], social phobia, affective disorders, and schizophrenia. In addition, DNA was included from 78 West Africans. The degree of admixture for each subject was estimated by analysis of a set of ancestry-informative genetic markers using the program STRUCTURE, and was compared between cases and controls. As noted previously, the degree of admixture in AAs was higher than EAs. In EAs, the degree of admixture (with African ancestry) was significantly lower in patients with SD (mainly AD) than controls (P = 0.009 for SD; P = 0.008 for AD). This finding suggests that population admixture may modulate risk for alcohol dependence. Population admixture might protect against alcohol dependence by increasing average heterozygosity and reducing the risk of deleterious recessive alleles. We cannot exclude the possibility that the results might have been influenced by selection bias due to the multisite nature of the study.
UR - http://www.scopus.com/inward/record.url?scp=67349112910&partnerID=8YFLogxK
U2 - 10.1007/s00439-009-0647-4
DO - 10.1007/s00439-009-0647-4
M3 - Article
C2 - 19306106
AN - SCOPUS:67349112910
SN - 0340-6717
VL - 125
SP - 605
EP - 613
JO - Human Genetics
JF - Human Genetics
IS - 5-6
ER -