Clinical Neuroscience Division, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Alcohol Clin Exp Res. 2012 Dec;36(12):2141-9. doi: 10.1111/j.1530-0277.2012.01823.x. Epub 2012 May 2.
Clinical trials for alcoholism have historically regarded alcohol consumption as the primary outcome. In a subset of trials, quality of life (QOL) has been considered as a secondary outcome. Joint latent-variable modeling techniques may provide a more accurate and powerful simultaneous analysis of primary and secondary outcomes in clinical trials. The goal of this study was to evaluate longitudinal associations between treatment status, alcohol consumption, and QOL in the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study.
A total of 1,383 alcohol-dependent patients were randomized to 9 treatment groups. Percent heavy drinking days (PHDD) and health-related QOL from the 30 days preceding baseline, week 16, and week 52 were calculated using the Form 90 and the Medical Outcomes Study Health Survey Short Form-12 (SF-12), respectively. Latent profile analysis (LPA) was conducted to determine an appropriate number of latent states to represent PHDD and QOL. Subsequently, univariate and coupled hidden Markov models (for PHDD and SF-12 mental health, and PHDD and SF-12 physical) were fit to the data.
LPA suggested that PHDD should be represented by 3 latent states and that each SF-12 scale should be represented by 2 states. Joint modeling results suggested that (i) naltrexone significantly predicted decreased PHDD (p < 0.05), and marginally predicted improved mental health QOL via decreased PHDD (p < 0.10), and (ii) that the combinations of naltrexone and combined behavioral intervention (CBI), and acamprosate and CBI, each predicted significantly improved physical QOL (p < 0.05), and marginally predicted decreased PHDD via improved physical QOL (p < 0.10).
This study illustrates a powerful and novel statistical approach for simultaneously evaluating the impact of treatments on primary and secondary outcomes in clinical trials. This study also suggests that behavioral interventions may impact drinking behavior through their ameliorative effects on QOL.
酒精中毒的临床试验历来将酒精摄入量视为主要结局。在部分试验中,生活质量(QOL)被视为次要结局。联合潜在变量建模技术可能为临床试验中主要和次要结局的更准确和强大的同时分析提供方法。本研究的目的是评估在联合药物治疗和行为干预治疗酒精依赖(COMBINE)研究中,治疗状况、酒精摄入量和 QOL 之间的纵向关联。
共 1383 名酒精依赖患者被随机分配到 9 个治疗组。使用 Form 90 和医疗结果研究健康调查短表-12(SF-12)分别计算基线前 30 天、第 16 周和第 52 周的重度饮酒天数(PHDD)和与健康相关的 QOL。采用潜在剖面分析(LPA)确定合适的潜在状态数量来代表 PHDD 和 QOL。随后,对数据进行单变量和耦合隐马尔可夫模型(用于 PHDD 和 SF-12 心理健康,以及 PHDD 和 SF-12 生理)拟合。
LPA 表明 PHDD 应由 3 个潜在状态表示,每个 SF-12 量表应由 2 个状态表示。联合建模结果表明:(i)纳曲酮显著预测 PHDD 减少(p<0.05),并且通过减少 PHDD 略微预测心理健康 QOL 改善(p<0.10);(ii)纳曲酮和联合行为干预(CBI)的组合,以及安非他酮和 CBI 的组合,都显著预测了生理 QOL 的改善(p<0.05),并且通过改善生理 QOL 略微预测了 PHDD 的减少(p<0.10)。
本研究说明了一种强大而新颖的统计方法,用于同时评估临床试验中治疗对主要和次要结局的影响。本研究还表明,行为干预可能通过改善 QOL 对饮酒行为产生影响。