Alcohol addiction and the mu-opioid receptor

被引:8
|
作者
Berrettini, Wade [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
关键词
Alcohol addiction; Genetics; Mu opioid receptor; Pharmacogenetics; SINGLE-NUCLEOTIDE POLYMORPHISM; GENE OPRM1; FUNCTIONAL POLYMORPHISM; NALTREXONE TREATMENT; A118G POLYMORPHISM; DEPENDENT SUBJECTS; NUCLEUS-ACCUMBENS; DOUBLE-BLIND; DBA/2; MICE; ETHANOL;
D O I
10.1016/j.pnpbp.2015.07.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
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 due to noncompliance, but many patients do not respond despite high levels of compliance. There are reports that a mis-sense 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 chapter 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. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:228 / 233
页数:6
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