Affiliation:
1. Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA
2. Interventional Pain Management, Northern Light Health, Brewer, ME, USA
3. Emergency Department, Emory University Hospital, Atlanta, GA, USA
Abstract
Background:Topiramate (TPM) has the potential to become one of the most prominent treatment options for alcohol use disorder (AUD). We investigated the efficacy of TPM for AUD treatment, considering new randomized controlled trials carried out since the publication of four prior investigations.Methods:We searched six major databases, comparing TPM to placebo for AUD treatment. We performed a Bayesian meta-analysis. We conducted a meta-regression, analyzing the effect of age, TPM dosage, duration of treatment, gender, and attrition rate on the outcomes measured. The protocol is registered with PROSPERO: CRD42021286266.Results:TPM reduced heavy drinking days ( d = 0.401, Bayes factor (BF) = 23.088) and weeks ( d = 0.461, BF = 3.784), lowered alcohol craving ( d = 0.477, BF = 107.749), prolonged abstinence throughout the duration of trials ( d = 0.505, BF = 54.998), and decreased the amount of gamma-glutamyl transferase in the blood ( d = 0.345, BF = 39.048). The analysis pointed out that TPM could reduce anxiety ( d = 0.517, BF = 5.993). TPM’s efficacy in relieving alcohol withdrawal, minimizing relapse, and decreasing depressive symptoms was inconclusive. There was evidence of a meta-regression effect of attrition rate on heavy drinking days and craving and length of treatment on abstinence.Conclusion:TPM has the potential to become a key pharmacological agent in the treatment of AUD.
Subject
Pharmacology (medical),Psychiatry and Mental health,Pharmacology
Cited by
10 articles.
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