N-Acetylcysteine for the Treatment of Co-Occurring Posttraumatic Stress Disorder and Alcohol Use Disorder: A Double-Blind, Randomized Controlled Trial.

IF 4.6 2区 医学 Q1 PSYCHIATRY
Sudie E Back, Kevin Gray, Amber M Jarnecke, Tanya C Saraiya, Elizabeth J Santa Ana, Therese Killeen, Jane E Joseph, James J Prisciandaro, Delisa G Brown, Paul J Nietert, Tracy Stecker, Alex Rothbaum, Jennifer L Jones, Julianne C Flanagan, Kathleen T Brady
{"title":"N-Acetylcysteine for the Treatment of Co-Occurring Posttraumatic Stress Disorder and Alcohol Use Disorder: A Double-Blind, Randomized Controlled Trial.","authors":"Sudie E Back, Kevin Gray, Amber M Jarnecke, Tanya C Saraiya, Elizabeth J Santa Ana, Therese Killeen, Jane E Joseph, James J Prisciandaro, Delisa G Brown, Paul J Nietert, Tracy Stecker, Alex Rothbaum, Jennifer L Jones, Julianne C Flanagan, Kathleen T Brady","doi":"10.4088/JCP.25m15803","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> Posttraumatic stress disorder (PTSD) and alcohol use disorder (AUD) are common co-occurring conditions associated with a more severe clinical profile and poorer treatment outcomes than either disorder alone. To date, no medications have proven efficacious in the treatment of co-occurring PTSD/AUD.</p><p><p><b>Methods:</b> This randomized, double-blind, placebo-controlled trial examined the efficacy of <i>N-</i>acetylcysteine (NAC; 2,400 mg/day) among individuals (N=182, aged 21-65 years) who met <i>DSM-5</i> criteria for current PTSD/AUD. Participants were randomized 1:1 to receive 12 weeks of NAC (n=93) or placebo (n=89). All participants received weekly, individual, cognitive behavioral therapy (CBT) for AUD. Follow-up visits occurred at 3-, 6-, and 12-months posttreatment. Primary outcomes included the Clinician Administered PTSD Scale for <i>DSM-5</i> (CAPS-5), PTSD Checklist for <i>DSM-5</i> (PCL-5), Timeline Follow-Back (TLFB), and the Obsessive Compulsive Drinking Scale at 12 weeks. The TLFB evaluated the frequency and amount of alcohol consumption. A secondary measure evaluated depression symptoms.</p><p><p><b>Results:</b> Intent-to-treat analyses showed that participants in both the NAC and placebo groups evidenced significant reductions in the CAPS-5 (B=-0.19, <i>P</i><.001) and PCL-5 (B=-0.20, <i>P</i><.001) during treatment, with no significant group differences. Both groups also showed significant reductions in alcohol use (drinks per drinking day [B=-0.02, <i>P</i><.001], percent heavy drinking days [B=-0.14, <i>P</i><.001], percent days abstinent [B=0.29, <i>P</i>=.022]) and craving (B=-0.12, <i>P</i><.001) during treatment, but with no significant group differences. There were no group differences in retention or adverse events.</p><p><p><b>Conclusions:</b> Although NAC was well tolerated, it was not more effective than placebo in improving symptoms of PTSD or AUD when added to individual CBT for AUD.</p><p><p><b>Trial Registration:</b> ClinicalTrials.gov identifier: NCT02966873.</p>","PeriodicalId":50234,"journal":{"name":"Journal of Clinical Psychiatry","volume":"86 4","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4088/JCP.25m15803","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Posttraumatic stress disorder (PTSD) and alcohol use disorder (AUD) are common co-occurring conditions associated with a more severe clinical profile and poorer treatment outcomes than either disorder alone. To date, no medications have proven efficacious in the treatment of co-occurring PTSD/AUD.

Methods: This randomized, double-blind, placebo-controlled trial examined the efficacy of N-acetylcysteine (NAC; 2,400 mg/day) among individuals (N=182, aged 21-65 years) who met DSM-5 criteria for current PTSD/AUD. Participants were randomized 1:1 to receive 12 weeks of NAC (n=93) or placebo (n=89). All participants received weekly, individual, cognitive behavioral therapy (CBT) for AUD. Follow-up visits occurred at 3-, 6-, and 12-months posttreatment. Primary outcomes included the Clinician Administered PTSD Scale for DSM-5 (CAPS-5), PTSD Checklist for DSM-5 (PCL-5), Timeline Follow-Back (TLFB), and the Obsessive Compulsive Drinking Scale at 12 weeks. The TLFB evaluated the frequency and amount of alcohol consumption. A secondary measure evaluated depression symptoms.

Results: Intent-to-treat analyses showed that participants in both the NAC and placebo groups evidenced significant reductions in the CAPS-5 (B=-0.19, P<.001) and PCL-5 (B=-0.20, P<.001) during treatment, with no significant group differences. Both groups also showed significant reductions in alcohol use (drinks per drinking day [B=-0.02, P<.001], percent heavy drinking days [B=-0.14, P<.001], percent days abstinent [B=0.29, P=.022]) and craving (B=-0.12, P<.001) during treatment, but with no significant group differences. There were no group differences in retention or adverse events.

Conclusions: Although NAC was well tolerated, it was not more effective than placebo in improving symptoms of PTSD or AUD when added to individual CBT for AUD.

Trial Registration: ClinicalTrials.gov identifier: NCT02966873.

n -乙酰半胱氨酸治疗创伤后应激障碍和酒精使用障碍:一项双盲、随机对照试验
目的:创伤后应激障碍(PTSD)和酒精使用障碍(AUD)是常见的共同发生的疾病,与单独的任何一种疾病相比,它们具有更严重的临床特征和更差的治疗结果。到目前为止,还没有药物被证明对合并PTSD/AUD的治疗有效。方法:这项随机、双盲、安慰剂对照试验检测了N-乙酰半胱氨酸(NAC; 2400 mg/天)在符合DSM-5当前PTSD/AUD标准的个体(N=182,年龄21-65岁)中的疗效。参与者以1:1的比例随机分配,接受12周的NAC (n=93)或安慰剂(n=89)。所有参与者每周接受单独的认知行为治疗(CBT)。随访时间分别为治疗后3个月、6个月和12个月。主要结果包括临床医生管理的DSM-5 PTSD量表(CAPS-5)、DSM-5 PTSD检查表(PCL-5)、时间线随访(TLFB)和12周时的强迫性饮酒量表。TLFB评估了饮酒的频率和数量。第二项测量评估抑郁症状。结果:意向治疗分析显示,NAC组和安慰剂组的参与者在cap -5 (B=-0.19, PPPPP= 0.022)和渴望(B=-0.12, p)方面都有显著降低。结论:尽管NAC耐受性良好,但在改善PTSD或AUD症状方面,NAC与单独的AUD CBT结合使用并不比安慰剂更有效。试验注册:ClinicalTrials.gov标识符:NCT02966873。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Clinical Psychiatry
Journal of Clinical Psychiatry 医学-精神病学
CiteScore
7.40
自引率
1.90%
发文量
0
审稿时长
3-8 weeks
期刊介绍: For over 75 years, The Journal of Clinical Psychiatry has been a leading source of peer-reviewed articles offering the latest information on mental health topics to psychiatrists and other medical professionals.The Journal of Clinical Psychiatry is the leading psychiatric resource for clinical information and covers disorders including depression, bipolar disorder, schizophrenia, anxiety, addiction, posttraumatic stress disorder, and attention-deficit/hyperactivity disorder while exploring the newest advances in diagnosis and treatment.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信