Opioid Pharmacogenetics of Alcohol Addiction

被引:6
|
作者
Berrettini, Wade [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2013年 / 3卷 / 07期
关键词
RECEPTOR GENE OPRM1; SINGLE-NUCLEOTIDE POLYMORPHISM; FUNCTIONAL POLYMORPHISM; NALTREXONE TREATMENT; A118G POLYMORPHISM; NUCLEUS-ACCUMBENS; DOUBLE-BLIND; DBA/2; MICE; MU; DEPENDENCE;
D O I
10.1101/cshperspect.a012203
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alcohol addiction is one of the most common and devastating diseases in the world. Given the tremendous heterogeneity of alcohol-addicted individuals, it is unlikely that one medication will help nearly all patients. Thus, there is a clear need to develop predictors of response to existing medications. Naltrexone is a mu-opioid receptor antagonist, which has been approved in the United States for treatment of alcohol addiction since 1994. It has limited efficacy, in part because of noncompliance, but many patients do not respond despite high levels of compliance. There are reports that a missense single nucleotide polymorphism (rs179919 or A118G) in the mu-opioid receptor gene predicts a favorable response to naltrexone if an individual carries a "G" allele. This work will review the evidence for this hypothesis. The data are promising that the "G" allele predisposes to a beneficial naltrexone response among alcohol-addicted persons, but additional research is needed to prove this hypothesis in prospective clinical trials.
引用
收藏
页数:9
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