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Influence of stress associated with chronic alcohol exposure on drinking.长期饮酒相关应激对饮酒的影响。
Neuropharmacology. 2017 Aug 1;122:115-126. doi: 10.1016/j.neuropharm.2017.04.028. Epub 2017 Apr 19.
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Predictors of Naltrexone Response in a Randomized Trial: Reward-Related Brain Activation, OPRM1 Genotype, and Smoking Status.随机试验中纳曲酮反应的预测因子:与奖赏相关的大脑激活、OPRM1 基因型和吸烟状况。
Neuropsychopharmacology. 2017 Dec;42(13):2640-2653. doi: 10.1038/npp.2017.74. Epub 2017 Apr 14.
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Neurobiology of addiction: a neurocircuitry analysis.成瘾的神经生物学:神经回路分析
Lancet Psychiatry. 2016 Aug;3(8):760-773. doi: 10.1016/S2215-0366(16)00104-8.
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A Test-Replicate Approach to Candidate Gene Research on Addiction and Externalizing Disorders: A Collaboration Across Five Longitudinal Studies.一种针对成瘾和外化性障碍候选基因研究的测试-重复方法:五项纵向研究的合作
Behav Genet. 2016 Sep;46(5):608-626. doi: 10.1007/s10519-016-9800-8. Epub 2016 Jul 21.
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Corticostriatal circuitry and habitual ethanol seeking.皮质纹状体回路与习惯性乙醇寻求行为
Alcohol. 2015 Dec;49(8):817-24. doi: 10.1016/j.alcohol.2015.03.003. Epub 2015 May 14.
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Increased mesolimbic cue-reactivity in carriers of the mu-opioid-receptor gene OPRM1 A118G polymorphism predicts drinking outcome: a functional imaging study in alcohol dependent subjects.携带阿片受体μ型基因 OPRM1 A118G 多态性的个体中边缘系统-伏隔核线索反应增加预示着饮酒结局:酒精依赖受试者的功能影像学研究。
Eur Neuropsychopharmacol. 2015 Aug;25(8):1128-35. doi: 10.1016/j.euroneuro.2015.04.013. Epub 2015 Apr 18.
7
Naltrexone vs Placebo for the Treatment of Alcohol Dependence: A Randomized Clinical Trial.纳曲酮与安慰剂治疗酒精依赖的随机临床试验。
JAMA Psychiatry. 2015 May;72(5):430-7. doi: 10.1001/jamapsychiatry.2014.3053.
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OPRM1 genotype and naltrexone response in depressed alcohol-dependent patients.伴有酒精依赖的抑郁症患者的OPRM1基因分型与纳曲酮反应
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The efficacy of acamprosate and naltrexone in the treatment of alcohol dependence, Europe versus the rest of the world: a meta-analysis.阿坎酸与纳曲酮治疗酒精依赖的疗效:欧洲与世界其他地区对比的荟萃分析
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10
Clinically relevant genetic biomarkers from the brain in alcoholism with representation on high resolution chromosome ideograms.来自酒精中毒患者大脑的具有临床相关性的基因生物标志物,并在高分辨率染色体 ideogram 上呈现。
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药物增强行为疗法治疗酒精使用障碍:纳曲酮、嗜酒者互诫协会促进和 OPRM1 基因变异。

Medication-enhanced behavior therapy for alcohol use disorder: Naltrexone, Alcoholics Anonymous Facilitation, and OPRM1 genetic variation.

机构信息

Section on Addiction Medicine, Department of Family Medicine, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA.

Clinical and Research Institute on Addictions, University at Buffalo, Buffalo, NY, USA.

出版信息

J Subst Abuse Treat. 2019 Sep;104:7-14. doi: 10.1016/j.jsat.2019.05.004. Epub 2019 May 4.

DOI:10.1016/j.jsat.2019.05.004
PMID:31370987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6684329/
Abstract

Medication-assisted behavior treatment for alcohol use disorder (AUD) holds promise to enhance the efficacy of medication and of behavior therapy when administered individually. The present study examines the treatment benefit of combined outpatient naltrexone (NTX) treatment with Alcoholics Anonymous Facilitation (AAF) behavior therapy, in the context of OPRM1 genotype. The minor OPRM1 Asp40 G-allele has been associated with greater positive reinforcing effects of alcohol consumption and greater alcohol craving, suggesting that individuals carrying the OPRM1 G allele may have an improved naltrexone response. Twenty patients, including 7 G-allele carriers, received 90 days of naltrexone with medication support and dispensing sessions, and ten AAF behavior therapy sessions. During treatment and the eight-week posttreatment follow-up, an overall increase in percent days abstinent was observed for the sample as a whole, but G-allele carriers reported relatively heavier drinking relative to other subjects. These findings suggest that this enhanced medication-assisted behavior treatment is a promising therapeutic combination, and mirror other recent findings that G-allele carriers may require more intensive treatment.

摘要

药物辅助行为治疗酒精使用障碍(AUD)有望提高药物和行为治疗的疗效,当单独使用时。本研究在 OPRM1 基因型的背景下,考察了联合门诊纳曲酮(NTX)治疗与嗜酒者互诫协会促进(AAF)行为治疗的治疗益处。OPRM1Asp40G-等位基因与酒精消费的正强化作用增加和酒精渴求增加有关,这表明携带 OPRM1G 等位基因的个体可能对纳曲酮反应更好。20 名患者,包括 7 名 G 等位基因携带者,接受了 90 天的纳曲酮药物支持和配药治疗,并接受了 10 次 AAF 行为治疗。在治疗和八周的治疗后随访期间,整个样本的禁欲天数百分比总体上有所增加,但 G 等位基因携带者报告的饮酒量相对高于其他受试者。这些发现表明,这种增强的药物辅助行为治疗是一种有前途的治疗组合,与其他最近的发现相呼应,即 G 等位基因携带者可能需要更密集的治疗。