Current pharmacological treatment approaches for alcohol dependence

被引:51
作者
Mueller, Christian A. [1 ]
Geisel, Olga [1 ]
Banas, Roman [1 ]
Heinz, Andreas [1 ]
机构
[1] Charite, Dept Psychiat, Campus Charite Mitte, D-10117 Berlin, Germany
关键词
alcohol dependence; pharmacotherapy; reduced drinking; relapse prevention; PLACEBO-CONTROLLED-TRIAL; RANDOMIZED CONTROLLED-TRIAL; SYNAPTIC VESICLE PROTEIN; ANTIEPILEPTIC DRUG LEVETIRACETAM; 5-HT3 ANTAGONIST ONDANSETRON; HIGH-DOSE BACLOFEN; DOUBLE-BLIND; BINDING-SITE; WITHDRAWAL SYNDROME; DOPAMINE RELEASE;
D O I
10.1517/14656566.2014.876008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: At present, the substances acamprosate, naltrexone and disulfiram are available for pharmacotherapy in alcohol dependence, but clinical studies found only modest effect sizes of these treatment options. Areas covered: This article focuses on current pharmacological treatment approaches for alcohol dependence, which have been evaluated in randomized, placebo-controlled trials (RCTs). Expert opinion: Besides the opioid system modulator nalmefene, which has recently been approved as a medication for the reduction of alcohol consumption, several compounds have been investigated in patients with alcohol dependence using a randomized, placebo-controlled design. In these studies, the antiepileptic drugs topiramate and gabapentin were found to be effective in improving several drinking-related outcomes, whereas levetiracetam failed to show efficacy in the treatment of alcohol dependence. Clinical studies using (low-dose) baclofen, a selective GABA-B receptor agonist, produced conflicting results, so that results of further trials are needed. Varenicline has also shown mixed results in two RCTs, but might possibly be useful in patients with comorbid nicotine dependence. The alpha 1 adrenergic antagonist prazosin is currently under investigation in alcohol dependence with and without comorbid posttraumatic stress disorder (PTSD). Finally, first clinical evidence suggests that the 5-HT3 antagonist ondansetron might possibly be used in future within a pharmacogenetic treatment approach in alcohol dependence.
引用
收藏
页码:471 / 481
页数:11
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