The sleep-anxiety dysregulation model of alcohol use disorder risk: A nine-year longitudinal machine learning study.

IF 4.9 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of affective disorders Pub Date : 2025-12-01 Epub Date: 2025-08-06 DOI:10.1016/j.jad.2025.120035
Nur Hani Zainal, Natalia Van Doren
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引用次数: 0

Abstract

Background: Sleep disturbances are a known risk factor for alcohol use, yet their long-term predictive value for alcohol use disorder (AUD)-especially in the context of co-occurring anxiety symptoms-remains understudied. The present study thus applied machine learning with internal validation to evaluate how sleep disturbances predict nine-year AUD symptoms in midlife adults. It also introduces the Sleep-Anxiety Dysregulation Model of AUD Risk, which posits that sleep and anxiety symptoms confer shared vulnerability via disrupted arousal regulation.

Method: Community-dwelling midlife adults (N = 1,054) completed clinical interviews, self-reports, and a seven-day actigraphy protocol to assess demographics, psychiatric symptoms, anxiety severity, subjective sleep, and objective actigraphy sleep indices. A five-fold nested cross-validated random forest identified potentially nonlinear and interactive predictors. The baseline model included 41 variables.

Results: The final multivariable model explained over two-fifths of the variance in nine-year AUD symptoms (R2 = 42.7%, 95% confidence intervals [40.1%-45.8%]). Key baseline predictors of nine-year AUD severity included lower rest-stage activity, sleep discontinuity and fragmentation patterns, and decreased active wake-stage physical movement. Other baseline predictors comprised younger age, higher generalized anxiety disorder, major depression, and panic disorder severity. No subjective sleep disturbances predicted nine-year AUD symptoms.

Conclusions: Results underscore the shared contribution of sleep and anxiety disturbances to long-term AUD risk. The proposed Sleep-Anxiety Dysregulation Model of AUD Risk offers an integrative framework suggesting that AUD symptoms may emerge via chronic arousal dysregulation, including heightened physiological reactivity. Externally validating this model may inform preventive strategies targeting distal risk processes underlying AUD.

酒精使用障碍风险的睡眠焦虑失调模型:一项为期9年的纵向机器学习研究。
背景:睡眠障碍是已知的酒精使用的危险因素,但其对酒精使用障碍(AUD)的长期预测价值——特别是在同时发生焦虑症状的情况下——仍未得到充分研究。因此,本研究应用内部验证的机器学习来评估睡眠障碍如何预测中年成年人的9年AUD症状。它还介绍了AUD风险的睡眠焦虑失调模型,该模型假设睡眠和焦虑症状通过扰乱唤醒调节赋予了共同的脆弱性。方法:社区居住的中年成年人(N = 1054)完成临床访谈、自我报告和为期7天的活动记录仪方案,以评估人口统计学、精神症状、焦虑严重程度、主观睡眠和客观活动记录仪睡眠指标。一个五层嵌套交叉验证随机森林识别潜在的非线性和交互预测。基线模型包括41个变量。结果:最终的多变量模型解释了9年AUD症状中超过五分之二的方差(R2 = 42.7 %,95 %置信区间[40.1 %-45.8 %])。9年AUD严重程度的关键基线预测因素包括休息阶段活动减少、睡眠不连续和碎片模式减少以及清醒阶段活跃的身体运动减少。其他基线预测因素包括年龄更小、更严重的广泛性焦虑症、重度抑郁症和恐慌症严重程度。没有主观睡眠障碍预测9年的AUD症状。结论:研究结果强调了睡眠和焦虑障碍对长期AUD风险的共同贡献。提出的AUD风险睡眠焦虑失调模型提供了一个综合框架,表明AUD症状可能通过慢性唤醒失调出现,包括生理反应性增强。外部验证该模型可以为针对AUD的远端风险过程的预防策略提供信息。
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来源期刊
Journal of affective disorders
Journal of affective disorders 医学-精神病学
CiteScore
10.90
自引率
6.10%
发文量
1319
审稿时长
9.3 weeks
期刊介绍: The Journal of Affective Disorders publishes papers concerned with affective disorders in the widest sense: depression, mania, mood spectrum, emotions and personality, anxiety and stress. It is interdisciplinary and aims to bring together different approaches for a diverse readership. Top quality papers will be accepted dealing with any aspect of affective disorders, including neuroimaging, cognitive neurosciences, genetics, molecular biology, experimental and clinical neurosciences, pharmacology, neuroimmunoendocrinology, intervention and treatment trials.
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