O'Malley Stephanie S, Robin Robert W, Levenson Aryeh L, GreyWolf Iva, Chance Lawrence E, Hodgkinson Colin A, Romano Denise, Robinson Jane, Meandzija Boris, Stillner Verner, Wu Ran, Goldman David
Yale University School of Medicine, Connecticut Mental Health Center, S202, 34 Park Street, New Haven, CT 06519, USA.
Alcohol Clin Exp Res. 2008 Jul;32(7):1271-83. doi: 10.1111/j.1530-0277.2008.00682.x.
Access to specialty alcoholism treatment in rural environments is limited and new treatment approaches are needed. The objective was to evaluate the efficacy of naltrexone alone and in combination with sertraline among Alaska Natives and other Alaskans living in rural settings. An exploratory aim examined whether the Asn40Asp polymorphism of the mu-opioid receptor gene (OPRM1) predicted response to naltrexone, as had been reported in Caucasians.
Randomized, controlled trial enrolling 101 Alaskans with alcohol dependence, including 68 American Indians/Alaska Natives. Participants received 16 weeks of either (1) placebo (placebo naltrexone + placebo sertraline), (2) naltrexone monotherapy (50 mg naltrexone + sertraline placebo) and (3) naltrexone + sertraline (100 mg) plus nine sessions of medical management and supportive advice. Primary outcomes included Time to First Heavy Drinking Day and Total Abstinence.
Naltrexone monotherapy demonstrated significantly higher total abstinence (35%) compared with placebo (12%, p = 0027) and longer, but not statistically different, Time to First Heavy Drinking Day (p = 0.093). On secondary measures, naltrexone compared with placebo demonstrated significant improvements in percent days abstinent (p = 0.024) and drinking-related consequences (p = 0.02). Combined sertraline and naltrexone did not differ from naltrexone alone. The pattern of findings was generally similar for the American Indian/Alaska Native subsample. Naltrexone treatment response was significant within the group of 75 individuals who were homozygous for OPRM1 Asn40 allele. There was a small number of Asp40 carriers, precluding statistical testing of the effect of this allele on response.
Naltrexone can be used effectively to treat alcoholism in remote and rural communities, with evidence of benefit for American Indians and Alaska Natives. New models of care incorporating pharmacotherapy could reduce important health disparities related to alcoholism.
农村地区获得专业酒精成瘾治疗的机会有限,需要新的治疗方法。目的是评估纳曲酮单独使用以及与舍曲林联合使用对阿拉斯加原住民和其他居住在农村地区的阿拉斯加人的疗效。一项探索性目标研究了μ-阿片受体基因(OPRM1)的Asn40Asp多态性是否如在高加索人中所报道的那样能预测对纳曲酮的反应。
一项随机对照试验,招募了101名酒精依赖的阿拉斯加人,其中包括68名美国印第安人/阿拉斯加原住民。参与者接受16周的以下治疗之一:(1)安慰剂(安慰剂纳曲酮 + 安慰剂舍曲林),(2)纳曲酮单药治疗(50毫克纳曲酮 + 舍曲林安慰剂),以及(3)纳曲酮 + 舍曲林(100毫克)加九次医疗管理和支持性建议。主要结局包括首次重度饮酒日的时间和完全戒酒情况。
与安慰剂组(12%,p = 0.027)相比,纳曲酮单药治疗的完全戒酒率显著更高(35%),首次重度饮酒日的时间更长但无统计学差异(p = 0.093)。在次要指标方面,与安慰剂相比,纳曲酮在戒酒天数百分比(p = 0.024)和饮酒相关后果(p = 0.02)方面有显著改善。舍曲林和纳曲酮联合使用与单独使用纳曲酮没有差异。美国印第安人/阿拉斯加原住民亚组的研究结果模式总体相似。在OPRM1 Asn40等位基因纯合的75名个体中,纳曲酮治疗反应显著。Asp40携带者数量较少,无法对该等位基因对反应的影响进行统计学检验。
纳曲酮可有效用于治疗偏远农村社区的酒精成瘾,对美国印第安人和阿拉斯加原住民有益。纳入药物治疗的新护理模式可减少与酒精成瘾相关的重要健康差距。