Placebo-Controlled Trial of Zonisamide for the Treatment of ... : Journal of Clinical Psychopharmacology (original) (raw)

Brief Reports

Arias, Albert J. MD; Feinn, Richard PhD; Oncken, Cheryl MD, MPH; Covault, Jonathan MD, PhD; Kranzler, Henry R. MD

From the Alcohol Research Center, Department of Psychiatry, University of Connecticut School of Medicine, Farmington, CT.

Received September 11, 2009; accepted after revision February 26, 2010.

Reprints: Albert J. Arias, MD, Alcohol Research Center, Department of Psychiatry, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT 06030-2103 (e-mail: [email protected]).

This study was funded by NIH grants P50 AA03510, M01 RR06192 (University of Connecticut General Clinical Research Center), and K24 AA13736 (to H.R.K.).

Abstract

Introduction:

Zonisamide is an anticonvulsant medication with GABAergic, glutamatergic, and monoaminergic effects. Zonisamide has also been shown to reduce alcohol intake in rodents and in risky drinkers in the context of a laboratory study. This pilot clinical trial evaluated the safety, tolerability, and efficacy of zonisamide for the treatment of alcohol dependence.

Methods:

Forty alcohol-dependent subjects (23 men) were randomly assigned to receive treatment with either placebo or zonisamide in a 12-week double-blind trial. Zonisamide was initiated at a dosage of 100 mg/d, which was increased by 100 mg/d every 2 weeks for 8 weeks to a maximum dosage of 500 mg/d. The medication was continued for 4 weeks at the target dosage and then tapered and discontinued. The primary outcomes were drinks per week, heavy drinking days per week, and abstinent days per week, which were measured using the Timeline Follow-Back method.

Results:

There was a significant medication by treatment week interaction effect favoring the zonisamide group for heavy drinking days (HDD; P = 0.012), drinks per week (P = 0.004), and alcohol urge scores (P = 0.006). There was not a significant effect on the number or rate of increase in abstinent days. There were no serious adverse events reported and zonisamide treatment was well tolerated.

Conclusion:

The findings provide preliminary support for the use of zonisamide to treat alcohol dependence. Efforts to replicate and extend these findings are warranted.