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Mecamylamine treatment for alcohol dependence: a randomized controlled trial

2017; Wiley; Volume: 113; Issue: 1 Linguagem: Inglês

10.1111/add.13943

1360-0443

Ismene L. Petrakis, Elizabeth Ralevski, Ralitza Gueorguieva, Stephanie S. O’Malley, Albert J. Arias, Kevin A. Sevarino, Jane S. Jane, Erin M. O’Brien, John H. Krystal,

Neurotransmitter Receptor Influence on Behavior

Abstract Background and aims The nicotinic acetylcholine receptor antagonist, mecamylamine, is a potential novel pharmacotherapy for alcohol use disorder. The aims were to compare alcohol consumption between mecamylamine and placebo and test if smoking status modified treatment effects. Design Out‐patient, randomized, double‐blind clinical trial for 12 weeks of treatment with mecamylamine (10 mg) ( n = 65) versus placebo ( n = 63). Setting Connecticut, USA. Participants Individuals had current alcohol dependence ( n = 128), had an average age of 48.5 [standard deviation (SD) = 9.4], 110 (85.9%) were men, and included 74 smokers (57.8%) and 54 non‐smokers (42.2%). Participants were randomized to mecamylamine 10 mg per day or placebo. All subjects also received medical management therapy administered by trained research personnel. Measurements Primary outcome was percentage of heavy drinking days during the last month of treatment; other outcomes included drinking days, drinks per drinking days, alcohol craving, smoking, symptoms of nicotine withdrawal and side effects. Findings There were no significant differences in the percentage of heavy drinking days at 3 months between the mecamylamine (mean = 18.4, SD = 29.0) and placebo treatment groups (mean = 20.4, SD = 29.2) [ F 1, 100 = 1.3, P = 0.25; effect size d = 0.07; mean difference = 2.06, 95% confidence interval (CI) = −8.96 to 13.08]. There were no significant differences in percentage of drinking days or in drinks per drinking day at month 3 between the mecamylamine and placebo groups; there were no significant interactions. Conclusions Mecamylamine 10 mg per day did not reduce alcohol consumption significantly in treatment‐seeking smokers and non‐smokers with alcohol use disorder.