Medications for treating alcohol use disorder: A narrative review

被引:16
作者
Kranzler, Henry R. [1 ,2 ,3 ]
Hartwell, Emily E. [1 ,2 ]
机构
[1] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA USA
[2] Crescenz VAMC, Mental Illness Res Educ & Clin Ctr, Vet Integrated Serv Network 4, Philadelphia, PA USA
[3] Univ Penn, Ctr Studies Addict, Perelman Sch Med, 3535 Market St, Philadelphia, PA 19104 USA
来源
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH | 2023年 / 47卷 / 07期
关键词
alcohol use disorder; medication-assisted treatment; medications; pharmacotherapy; PLACEBO-CONTROLLED TRIAL; OPIOID RECEPTOR GENE; EXTENDED-RELEASE NALTREXONE; DOUBLE-BLIND; TARGETED NALTREXONE; DEPENDENT PATIENTS; DISULFIRAM TREATMENT; RELAPSE PREVENTION; HEAVY DRINKERS; ORAL NALMEFENE;
D O I
10.1111/acer.15118
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Chronic heavy alcohol use impacts all major neurotransmitter systems and is associated with multiple medical, psychiatric, and social problems. Available evidence-based medications to treat alcohol use disorder (AUD) are underutilized in clinical practice. These medications promote abstinence or reduce alcohol consumption, though there are questions regarding their optimal dosage, length of treatment, and utility in combination with one another. Pharmacogenetic approaches, which use a patient's genetic make-up to inform medication selection, have garnered great interest but have yet to yield results robust enough to incorporate them in routine clinical care. This narrative review summarizes the evidence both for medications approved by the Food and Drug Administration (disulfiram, oral naltrexone, acamprosate, and extended-release naltrexone) and those commonly used off-label (e.g., gabapentin, baclofen, and topiramate) for AUD treatment. We discuss these drugs' mechanisms of action, clinical use, pharmacogenetic findings, and treatment recommendations. We conclude that the most consistent evidence supporting the pharmacotherapy of AUD is for the opioid antagonists, naltrexone and nalmefene (which is not approved in the United States), and topiramate. These medications demonstrate consistent small or moderate effects in reducing the frequency of drinking and/or heavy drinking. Lastly, we make suggestions for research needed to refine and expand the current literature on effective pharmacotherapy for AUD.
引用
收藏
页码:1224 / 1237
页数:14
相关论文
共 118 条
  • [1] Ahmed Saeed, 2019, Prim Care Companion CNS Disord, V21, DOI 10.4088/PCC.19r02465
  • [2] TECHNIQUES TO ENHANCE COMPLIANCE WITH DISULFIRAM
    ALLEN, JP
    LITTEN, RZ
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1992, 16 (06) : 1035 - 1041
  • [3] An evaluation of μ-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence
    Anton, Raymond F.
    Oroszi, Gabor
    O'Malley, Stephanie
    Couper, David
    Swift, Robert
    Pettinati, Helen
    Goldman, David
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2008, 65 (02) : 135 - 144
  • [4] A randomized, multicenter, double-blind, placebo-controlled study of the efficacy and safety of aripiprazole for the treatment of alcohol dependence
    Anton, Raymond F.
    Kranzler, Henry
    Breder, Christopher
    Marcus, Ronald N.
    Carson, William H.
    Han, Jian
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2008, 28 (01) : 5 - 12
  • [5] Efficacy of Gabapentin for the Treatment of Alcohol Use Disorder in Patients With Alcohol Withdrawal Symptoms A Randomized Clinical Trial
    Anton, Raymond F.
    Latham, Patricia
    Voronin, Konstantin
    Book, Sarah
    Hoffman, Michaela
    Prisciandaro, James
    Bristol, Emily
    [J]. JAMA INTERNAL MEDICINE, 2020, 180 (05) : 728 - 736
  • [6] Gabapentin Combined With Naltrexone for the Treatment of Alcohol Dependence
    Anton, Raymond F.
    Myrick, Hugh
    Wright, Tara M.
    Latham, Patricia K.
    Baros, Alicia M.
    Waid, L. Randolph
    Randall, Patrick K.
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2011, 168 (07) : 709 - 717
  • [7] Combined pharmacotherapies and behavioral interventions for alcohol dependence - The COMBINE study: A randomized controlled trial
    Anton, RF
    O'Malley, SS
    Ciraulo, DA
    Cisler, RA
    Couper, D
    Donovan, DM
    Gastfriend, DR
    Hosking, JD
    Johnson, BA
    LoCastro, JS
    Longabaugh, R
    Mason, BJ
    Mattson, ME
    Miller, WR
    Pettinati, HM
    Randall, CL
    Swift, R
    Weiss, RD
    Williams, LD
    Zweben, A
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (17): : 2003 - 2017
  • [8] A multi-site dose ranging study of nalmefene in the treatment of alcohol dependence
    Anton, RF
    Pettinati, H
    Zweben, A
    Kranzler, HR
    Johnson, B
    Bohn, MJ
    McCaul, ME
    Anthenelli, R
    Salloum, I
    Galloway, G
    Garbutt, J
    Swift, R
    Gastfriend, D
    Kallio, A
    Karhuvaara, S
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2004, 24 (04) : 421 - 428
  • [9] Posttreatment results of combining naltrexone with cognitive-behavior therapy for the treatment of alcoholism
    Anton, RF
    Moak, DH
    Latham, PK
    Waid, LR
    Malcolm, RJ
    Dias, JK
    Roberts, JS
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2001, 21 (01) : 72 - 77
  • [10] Effects of opioid receptor gene variation on targeted nalmefene treatment in heavy drinkers
    Arias, Albert J.
    Armeli, Stephen
    Gelernter, Joel
    Covault, Jonathan
    Kallio, Antero
    Karhuvaara, Sakari
    Koivisto, Tiina
    Makela, Rauno
    Kranzler, Henry R.
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2008, 32 (07) : 1159 - 1166