OPRM1;
5-HTTLPR;
GABRA2;
ALDH2;
ADH1B;
Level of response to alcohol;
MU-OPIOID-RECEPTOR;
SINGLE-NUCLEOTIDE POLYMORPHISM;
NATIONAL EPIDEMIOLOGIC SURVEY;
COGNITIVE-BEHAVIORAL THERAPY;
SEROTONIN TRANSPORTER GENE;
FUNCTIONAL POLYMORPHISM;
METABOLIZING GENES;
DOPAMINE RELEASE;
UNITED-STATES;
DOUBLE-BLIND;
D O I:
10.1016/j.pbb.2013.11.001
中图分类号:
B84 [心理学];
C [社会科学总论];
Q98 [人类学];
学科分类号:
03 ;
0303 ;
030303 ;
04 ;
0402 ;
摘要:
Although very many individuals drink alcohol at safe levels, a significant proportion escalates their consumption with addiction as the end result. Alcoholism is a common, moderately heritable, psychiatric disorder that is accompanied by considerable morbidity and mortality. Variation in clinical presentation suggests inter-individual variation in mechanisms of vulnerability including genetic risk factors. The development of addiction is likely to involve numerous functional genetic variants of small effects. The first part of this review will focus on genetic factors underlying inter-individual variability in response to alcohol consumption, including variants in alcohol metabolizing genes that produce an aversive response (the flushing syndrome) and variants that predict the level of subjective and physiological response to alcohol. The second part of this review will report on genetic variants that identify subgroups of alcoholics who are more likely to respond to pharmacotherapy to reduce levels of drinking or maintain abstinence. Genetic analyses of the level of response to alcohol, particularly of the functional OPRM1 A118G polymorphism and 5' and 3' functional polymorphisms in SLC6A4, are beginning to provide insights into the etiology of alcoholism and also genotype-stratified subgroup responses to naltrexone and SSRIs/ondansetron respectively. Because of large inter-ethnic variation in allele frequencies, the relevance of these functional polymorphisms will vary between ethnic groups. However there are relatively few published studies in this field, particularly with large sample sizes in pharmacogenetic studies, therefore it is premature to draw any conclusions at this stage. Published by Elsevier Inc.
机构:
Brown Univ, Ctr Alcohol & Addict Studies, Providence, RI 02912 USA
VA Med Ctr, Providence, RI USABrown Univ, Ctr Alcohol & Addict Studies, Providence, RI 02912 USA
Swift, R. M.
Ray, L. A.
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机构:
Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90024 USABrown Univ, Ctr Alcohol & Addict Studies, Providence, RI 02912 USA
机构:
Columbia Univ, New York State Psychiat Inst, New York, NY 10032 USA
Columbia Univ, Dept Psychiat, Coll Phys & Surg, New York, NY 10032 USAColumbia Univ, New York State Psychiat Inst, New York, NY 10032 USA
Evans, Suzette M.
Levin, Frances R.
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机构:
Columbia Univ, New York State Psychiat Inst, New York, NY 10032 USA
Columbia Univ, Dept Psychiat, Coll Phys & Surg, New York, NY 10032 USAColumbia Univ, New York State Psychiat Inst, New York, NY 10032 USA
机构:
Virginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Dept Psychiat, Richmond, VA 23298 USAVirginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Dept Psychiat, Richmond, VA 23298 USA
Prescott, CA
Kendler, KS
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机构:
Virginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Dept Psychiat, Richmond, VA 23298 USAVirginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Dept Psychiat, Richmond, VA 23298 USA