Judith Zaiser, Sabine Hoffmann, Sina Zimmermann, Tatjana Gessner, Milena Deck, Nina Kim Bekier, Martin Abel, Philipp Radler, Jens Langejürgen, Bernd Lenz, Sabine Vollstädt-Klein, Jan Stallkamp, Clemens Kirschbaum, Falk Kiefer, Patrick Bach
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We conducted a randomized-controlled experimental study to compare the effects of psychosocial stress against physical stress and a control intervention, each followed by an alcohol cue-exposure, on alcohol craving, subjective stress and saliva cortisol levels (main outcomes) in N = 121 individuals with AUD and collected data on daily alcohol use and craving during a 1-year ambulatory assessment phase. We applied linear mixed models to compare the effects of experimental interventions on the main outcomes and the relative contributions of the observed changes on the main outcomes to predicting stress and alcohol craving during the experiment and alcohol use and craving during the ambulatory assessment phase. Sequential exposure to psychosocial stress and alcohol cues induced higher cortisol levels (F<sub>(10,580)</sub> = 10.819, p < 0.001), subjective stress (F<sub>(2,117)</sub> = 10.520, p < 0.001) and alcohol craving (F<sub>(6,348)</sub> = 4.313, p < 0.001) compared to the exposure to physical stress and the control condition. Subjective stress reactivity was the most influential predictor of craving during the experiment (F<sub>(1,92)</sub> = 9.43, p = 0.003) and during the ambulatory phase (β = 0.16, p = 0.039) while cortisol levels predicted alcohol consumption in real-life settings (β = 9.76, p = 0.043). 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引用次数: 0
摘要
在酒精使用障碍(AUD)中,压力和酒精提示会引发酒精渴望和酒精消费。然而,它们在生理和心理层面上的相互作用,以及它们在现实生活中对日常酒精渴望和酒精使用的影响,目前还不清楚。我们进行了一项随机对照实验研究,比较心理社会压力对身体压力和对照干预的影响,每个干预都紧接着酒精提示暴露,对N = 121名AUD患者的酒精渴望、主观压力和唾液皮质醇水平(主要结果)的影响,并在1年的门诊评估阶段收集了每日酒精使用和渴望的数据。我们应用线性混合模型来比较实验干预对主要结果的影响,以及观察到的变化对主要结果的相对贡献,以预测实验期间的压力和酒精渴望,以及动态评估阶段的酒精使用和渴望。连续暴露于心理社会压力和酒精提示诱导较高的皮质醇水平(F(10,580) = 10.819, p (2,117) = 10.520, p (6,348) = 4.313, p (1,92) = 9.43, p = 0.003)和在流动阶段(β = 0.16, p = 0.039),而皮质醇水平预测现实生活中的酒精摄入量(β = 9.76, p = 0.043)。我们的研究结果强调了心理社会压力对线索诱导的渴望以及主观和神经内分泌应激反应的影响,并证明了现实生活中主观和神经内分泌应激反应与酒精渴望和酒精使用之间的联系。
Individual stress reactivity predicts alcohol craving and alcohol consumption in alcohol use disorder in experimental and real-life settings.
Stress- and alcohol cues trigger alcohol craving and alcohol consumption in alcohol use disorder (AUD). However, their interactions on a physiological and psychological level and their effects on daily alcohol craving and alcohol use in real-life situations are not understood yet. We conducted a randomized-controlled experimental study to compare the effects of psychosocial stress against physical stress and a control intervention, each followed by an alcohol cue-exposure, on alcohol craving, subjective stress and saliva cortisol levels (main outcomes) in N = 121 individuals with AUD and collected data on daily alcohol use and craving during a 1-year ambulatory assessment phase. We applied linear mixed models to compare the effects of experimental interventions on the main outcomes and the relative contributions of the observed changes on the main outcomes to predicting stress and alcohol craving during the experiment and alcohol use and craving during the ambulatory assessment phase. Sequential exposure to psychosocial stress and alcohol cues induced higher cortisol levels (F(10,580) = 10.819, p < 0.001), subjective stress (F(2,117) = 10.520, p < 0.001) and alcohol craving (F(6,348) = 4.313, p < 0.001) compared to the exposure to physical stress and the control condition. Subjective stress reactivity was the most influential predictor of craving during the experiment (F(1,92) = 9.43, p = 0.003) and during the ambulatory phase (β = 0.16, p = 0.039) while cortisol levels predicted alcohol consumption in real-life settings (β = 9.76, p = 0.043). Our results highlight the impact of psychosocial stress on cue-induced craving and subjective and neuroendocrine stress responses and demonstrate links between subjective and neuroendocrine stress-reactivity and alcohol craving and alcohol use in real-life settings.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.