Gabapentinoids for treatment of alcohol use disorder: A systematic review and meta-analysis

被引:17
作者
Cheng, Ying-Chih [1 ,2 ,3 ,4 ]
Huang, Yu-Chen [4 ,5 ,6 ,7 ]
Huang, Wei-Lieh [8 ,9 ,10 ,11 ]
机构
[1] Minist Hlth & Welf, Dept Psychiat, Taoyuan Psychiat Ctr, Taoyuan, Taiwan
[2] Natl Taiwan Univ, Coll Publ Hlth, Dept Publ Hlth, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Publ Hlth, Inst Epidemiol & Prevent Med, Taipei, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Res Ctr Big Data & Meta Anal, Taipei, Taiwan
[5] Taipei Med Univ, Wan Fang Hosp, Dept Dermatol, Taipei, Taiwan
[6] Taipei Med Univ, Dept Dermatol, Sch Med, Taipei, Taiwan
[7] Taipei Med Univ, Coll Med, Taipei, Taiwan
[8] Natl Taiwan Univ Hosp, Yunlin Branch, Dept Psychiat, 579,Sec 2,Yunlin Rd, Touliu 640, Yunlin, Taiwan
[9] Natl Taiwan Univ Hosp, Dept Psychiat, Taipei, Taiwan
[10] Natl Taiwan Univ, Coll Med, Dept Psychiat, Taipei, Taiwan
[11] Natl Taiwan Univ, Coll Med, Grad Inst Clin Med, Taipei, Taiwan
关键词
alcohol use disorder; alcohol withdrawal; craving; gabapentin; pregabalin; WITHDRAWAL SYNDROME; DOUBLE-BLIND; RELAPSE PREVENTION; PREGABALIN; DEPENDENCE; EFFICACY; NALTREXONE; TRIAL; DETOXIFICATION; ACAMPROSATE;
D O I
10.1002/hup.2751
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective Gabapentin (GBP) and pregabalin (PGB) have been used to treat alcohol use disorder (AUD) and alcohol withdrawal, but with inconsistent results. In this meta-analysis, we explored the effects of GBP/PGB treatment on AUD and their effects on withdrawal, craving, depression, and sleep disturbance in AUD patients. Methods We carried out a systematic review and meta-analysis of randomized controlled trials comparing the effects of GBP/PGB on AUD with those of a placebo or control treatment. Electronic databases were searched for relevant articles published before September 2019. The primary outcome was defined as the efficacy measure on achieving abstinence or reducing alcohol consumption in a hierarchical order. We included 16 studies in our meta-analysis. Results Overall, GBP had no significant benefit comparing to placebo or control treatment (Hedges'g= 0.0725,p= 0.6743). For specific alcohol-related outcome, GBP had significant effect on percentage of heavy drink (Hedges'g= 0.5478,p= 0.0441) and alcohol withdrawal symptoms (Hedges'g= 0.2475,p= 0.0425). GBP/PGB did not have significant beneficial effect on craving, depressive symptoms, or sleep disturbance. Instability was shown in sensitivity analyses of some above results. Conclusions GBP may be helpful to reduce AUD patients' heavy drinking behavior and withdrawal, but more studies are needed for drawing conclusions.
引用
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页码:1 / 11
页数:11
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