Pharmacogenetics of alcohol use disorders and comorbid psychiatric disorders

被引:13
|
作者
Helton, Sarah G. [1 ]
Lohoff, Falk W. [1 ]
机构
[1] NIAAA, Lab Clin Genom & Expt Therapeut, NIH, Bethesda, MD USA
关键词
Pharmacotherapy; Alcohol dependence; Treatment response; Psychiatric comorbidity; Genetics; Personalized medicine; PLACEBO-CONTROLLED TRIAL; RANDOMIZED CONTROLLED-TRIAL; NATIONAL EPIDEMIOLOGIC SURVEY; TRANSCRIPTION FACTOR GATA4; DOPAMINE-BETA-HYDROXYLASE; GENOME-WIDE ASSOCIATION; OPIOID-RECEPTOR OPRM1; DOUBLE-BLIND; DEPENDENT PATIENTS; MAJOR DEPRESSION;
D O I
10.1016/j.psychres.2015.09.019
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Alcohol use disorders (AUDs) represent a significant health burden worldwide. Currently, there are three medications approved by the U.S. Food and Drug Administration for the treatment of AUDs, and other drugs are being prescribed off-label for this purpose. However, response rates for pharmacologic treatment are low, and extant research suggests that treatment effects may partially depend on genetic factors. Personalized medicine, or using a patient's genetics and/or personal history to determine efficacy of treatment prior to prescription, is an emerging tool that will help clinicians treat their patients more effectively and safely. This review systematically discusses current findings from AUD pharmacotherapy trials examining disulfiram, acamprosate, naltrexone, the injectable naltrexone, and topiramate. Furthermore, it presents pharmacogenetics findings associated with these medications in an attempt to further the field of personalized medicine. Research from trials examining AUDs and comorbid major depressive disorder and anxiety disorders is also presented, and pharmacogenetic findings for these treatments are discussed. Lastly, the authors comment on the present and future states of the field of personalized medicine for AUD. Published by Elsevier Ireland Ltd.
引用
收藏
页码:121 / 129
页数:9
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