Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut.
Alcohol Clin Exp Res. 2019 Apr;43(4):741-746. doi: 10.1111/acer.13969. Epub 2019 Feb 19.
The noradrenergic system has been implicated in alcohol use disorder (AUD) and posttraumatic stress disorder (PTSD), with adrenergic agents reducing drinking in individuals with AUD and improving sleep disturbances in individuals with PTSD. In a recent clinical trial, prazosin, an α1-adrenergic antagonist, was not superior to placebo in reducing PTSD symptoms, sleep problems, or alcohol consumption in a comorbid population; however, patients in both treatment conditions improved in all symptom domains over the course of treatment. It remains unknown whether alcohol abstinence is related to changes in PTSD symptoms and medication effects in individuals with this comorbidity.
Veterans with comorbid alcohol dependence and PTSD (n = 96) were randomized to prazosin (16 mg) or placebo in a 12-week outpatient, double-blind clinical trial. In this secondary data analysis, we examined main effects of alcohol abstainer status (abstainer vs. nonabstainer), treatment, and their interaction on changes in PTSD symptoms over time using linear mixed models.
There was a main effect of alcohol abstainer status on symptoms of PTSD (p = 0.03), such that nonabstainers had lower total Clinician-Administered PTSD Scale (CAPS) scores than abstainers. There was a significant treatment by alcohol abstainer status interaction (p = 0.01); specifically, among placebo-treated individuals, those who did not abstain from alcohol had lower total CAPS scores compared to alcohol abstainers. Within the prazosin-treated group, abstainers and nonabstainers did not differ on total CAPS scores. Results were similar for the avoidance (p = 0.02), reexperiencing (p = 0.01), and hyperarousal (p = 0.04) subscales, such that placebo-treated nonabstainers had lower CAPS scores overall.
Overall, prazosin treatment was not significantly related to changes in PTSD symptoms over the course of the 12-week clinical trial in a comorbid population. Interestingly, placebo-treated alcohol nonabstainers had a significant reduction in PTSD symptoms. Whether placebo-treated individuals continued to use alcohol because of ongoing symptoms of PTSD is not known.
去甲肾上腺素能系统与酒精使用障碍(AUD)和创伤后应激障碍(PTSD)有关,肾上腺素能药物可减少 AUD 患者的饮酒量,并改善 PTSD 患者的睡眠障碍。在最近的一项临床试验中,α1-肾上腺素能拮抗剂普萘洛尔在减少 PTSD 症状、睡眠问题或共病人群的饮酒量方面并不优于安慰剂;然而,在治疗过程中,两种治疗条件下的患者在所有症状领域都有所改善。目前尚不清楚在共病患者中,酒精戒断是否与 PTSD 症状的变化和药物治疗效果有关。
共患有酒精依赖和 PTSD 的退伍军人(n=96)被随机分配到普萘洛尔(16mg)或安慰剂的 12 周门诊、双盲临床试验中。在这项二次数据分析中,我们使用线性混合模型检查了酒精戒断状态(戒断者与非戒断者)、治疗和它们之间相互作用对随时间变化的 PTSD 症状的主要影响。
酒精戒断状态对 PTSD 症状有主要影响(p=0.03),即非戒断者的总体临床医生管理 PTSD 量表(CAPS)评分低于戒断者。治疗与酒精戒断状态之间存在显著的相互作用(p=0.01);具体来说,在接受安慰剂治疗的个体中,那些没有戒断酒精的人比戒断酒精的人 CAPS 总分更低。在普萘洛尔治疗组中,戒断者和非戒断者在 CAPS 总分上没有差异。回避(p=0.02)、再体验(p=0.01)和过度警觉(p=0.04)分量表的结果相似,即接受安慰剂治疗的非戒断者总体上 CAPS 评分较低。
总的来说,在共病人群的 12 周临床试验中,普萘洛尔治疗与 PTSD 症状的变化没有显著关系。有趣的是,接受安慰剂治疗的酒精非戒断者 PTSD 症状显著减轻。不知道接受安慰剂治疗的个体是否因为 PTSD 的持续症状而继续饮酒。