Witkiewitz Katie, Hallgren Kevin A, Kranzler Henry R, Mann Karl F, Hasin Deborah S, Falk Daniel E, Litten Raye Z, O'Malley Stephanie S, Anton Raymond F
Department of Psychology, University of New Mexico, Albuquerque, New Mexico.
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.
Alcohol Clin Exp Res. 2017 Jan;41(1):179-186. doi: 10.1111/acer.13272. Epub 2016 Dec 26.
Alcohol use disorder (AUD) is a highly prevalent public health problem associated with considerable individual and societal costs. Abstinence from alcohol is the most widely accepted target of treatment for AUD, but it severely limits treatment options and could deter individuals who prefer to reduce their drinking from seeking treatment. Clinical validation of reduced alcohol consumption as the primary outcome of alcohol clinical trials is critical for expanding treatment options. One potentially useful measure of alcohol treatment outcome is a reduction in the World Health Organization (WHO, International Guide for Monitoring Alcohol Consumption and Related Harm. Geneva, Switzerland, 2000) risk levels of alcohol use (very high risk, high risk, moderate risk, and low risk). For example, a 2-shift reduction in WHO risk levels (e.g., high risk to low risk) has been used by the European Medicines Agency (2010, Guideline on the Development of Medicinal Products for the Treatment of Alcohol Dependence. UK) to evaluate nalmefene as a treatment for alcohol dependence (AD; Mann et al. 2013, Biol Psychiatry 73, 706-13).
The current study was a secondary data analysis of the COMBINE study (n = 1,383; Anton et al., ) to examine the association between reductions in WHO risk levels and reductions in alcohol-related consequences and mental health symptoms during and following treatment in patients with AD.
Any reduction in WHO risk drinking level during treatment was associated with significantly fewer alcohol-related consequences and improved mental health at the end of treatment and for up to 1 year posttreatment. A greater reduction in WHO risk drinking level predicted a greater reduction in consequences and greater improvements in mental health.
Changes in WHO risk levels appear to be a valid end point for alcohol clinical trials. Based on the current findings, reductions in WHO risk drinking levels during treatment reflect meaningful reductions in alcohol-related consequences and improved functioning.
酒精使用障碍(AUD)是一个高度普遍的公共卫生问题,会带来相当大的个人和社会成本。戒酒是治疗AUD最广泛接受的目标,但它严重限制了治疗选择,可能会阻碍那些希望减少饮酒量的人寻求治疗。将减少酒精摄入量作为酒精临床试验的主要结果进行临床验证,对于扩大治疗选择至关重要。一种潜在有用的酒精治疗结果衡量指标是世界卫生组织(WHO,《酒精消费及相关危害监测国际指南》。瑞士日内瓦,2000年)酒精使用风险水平(极高风险、高风险、中度风险和低风险)的降低。例如,欧洲药品管理局(2010年,《酒精依赖治疗用药品开发指南》。英国)已使用WHO风险水平降低两级(如,从高风险降至低风险)来评估纳美芬作为酒精依赖(AD)的一种治疗方法(Mann等人,2013年,《生物精神病学》73卷,706 - 13页)。
本研究是对联合研究(n = 1383;Anton等人)的二次数据分析,以检验AD患者在治疗期间及治疗后WHO风险水平降低与酒精相关后果及心理健康症状减轻之间的关联。
治疗期间WHO风险饮酒水平的任何降低都与治疗结束时以及治疗后长达1年时显著减少的酒精相关后果和改善的心理健康相关。WHO风险饮酒水平降低幅度越大,后果减少幅度越大,心理健康改善越明显。
WHO风险水平的变化似乎是酒精临床试验的一个有效终点。基于当前研究结果,治疗期间WHO风险饮酒水平的降低反映了酒精相关后果的显著减少和功能改善。