Suppr超能文献

双盲、随机试验中舍曲林治疗酒精依赖的治疗后结果。

Post-treatment outcomes in a double-blind, randomized trial of sertraline for alcohol dependence.

机构信息

Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, USA.

出版信息

Alcohol Clin Exp Res. 2012 Apr;36(4):739-44. doi: 10.1111/j.1530-0277.2011.01659.x. Epub 2011 Oct 7.

Abstract

BACKGROUND

Pharmacotherapy studies in alcohol dependence (AD) are generally of short duration and do not include post-treatment follow-up. We examined the durability of treatment effects in a placebo-controlled trial of sertraline for AD.

METHODS

As previously reported, patients received 12 weeks of treatment with sertraline (n = 63) or placebo (n = 71), followed by assessments at 3 and 6 months post-treatment (Kranzler et al., 2011, J Clin Psychopharmacol 31:22-30). We examined the main and interaction effects with time of 3 between-subject factors (medication group, age of onset of AD [late-onset alcoholics, LOAs, vs. early-onset alcoholics, EOAs], and the tri-allelic 5-HTTLPR genotype) on drinking days (DDs) and heavy drinking days (HDDs).

RESULTS

The medication group effect, which was significant during treatment, remained significant during the 3-month follow-up period for L'/L' LOAs, with the sertraline group having fewer DDs than the placebo group (p = 0.027). However, the medication group effect seen in L'/L' EOAs during treatment was no longer significant (p = 0.48). There were no significant effects in S' carriers at the 3-month follow-up visit, or in either genotype group at the 6-month follow-up.

CONCLUSIONS

The beneficial effects of sertraline observed in LOAs during treatment persisted during the 3-month post-treatment period. Additional studies are needed to validate these pharmacogenetic findings, which together with the effects seen during active treatment support the use of sertraline only in LOAs.

摘要

背景

酒精依赖(AD)的药物治疗研究通常持续时间较短,并且不包括治疗后随访。我们在一项舍曲林治疗 AD 的安慰剂对照试验中检查了治疗效果的持久性。

方法

如先前报道,患者接受舍曲林(n=63)或安慰剂(n=71)治疗 12 周,随后在治疗后 3 个月和 6 个月进行评估(Kranzler 等人,2011 年,J Clin Psychopharmacol 31:22-30)。我们检查了 3 个受试者间因素(药物组、AD 发病年龄[晚发性酗酒者,LOAs,与早发性酗酒者,EOAs]和三等位 5-HTTLPR 基因型)与时间的主要和交互作用对饮酒天数(DDs)和大量饮酒天数(HDDs)的影响。

结果

在治疗期间有统计学意义的药物组效应在 3 个月的随访期间对 L'/L' LOAs 仍然显著,舍曲林组的 DDs 少于安慰剂组(p=0.027)。然而,在治疗期间 L'/L' EOAs 中观察到的药物组效应不再显著(p=0.48)。在 3 个月随访时,S'携带者没有显著影响,在 6 个月随访时,在任何基因型组中也没有显著影响。

结论

在治疗期间观察到 LOAs 中舍曲林的有益作用在治疗后 3 个月持续存在。需要进一步的研究来验证这些药物遗传学发现,这些发现与治疗期间的效果一起支持仅在 LOAs 中使用舍曲林。

相似文献

1
Post-treatment outcomes in a double-blind, randomized trial of sertraline for alcohol dependence.
Alcohol Clin Exp Res. 2012 Apr;36(4):739-44. doi: 10.1111/j.1530-0277.2011.01659.x. Epub 2011 Oct 7.
3
5-HTTLPR genotype and daily negative mood moderate the effects of sertraline on drinking intensity.
Addict Biol. 2013 Nov;18(6):1024-31. doi: 10.1111/adb.12007. Epub 2012 Nov 12.
4
A within-group design of nontreatment seeking 5-HTTLPR genotyped alcohol-dependent subjects receiving ondansetron and sertraline.
Alcohol Clin Exp Res. 2009 Feb;33(2):315-23. doi: 10.1111/j.1530-0277.2008.00835.x. Epub 2008 Nov 19.
5
Treatment outcomes in type A and B alcohol dependence 6 months after serotonergic pharmacotherapy.
Alcohol Clin Exp Res. 2004 Jul;28(7):1065-73. doi: 10.1097/01.alc.0000130974.50563.04.
9
Comparison of alcoholism subtypes as moderators of the response to sertraline treatment.
Alcohol Clin Exp Res. 2012 Mar;36(3):509-16. doi: 10.1111/j.1530-0277.2011.01609.x. Epub 2011 Sep 6.
10
Sertraline and cognitive behavioral therapy for depressed alcoholics: results of a placebo-controlled trial.
J Clin Psychopharmacol. 2003 Dec;23(6):553-62. doi: 10.1097/01.jcp.0000095346.32154.41.

引用本文的文献

1
Off-label and investigational drugs in the treatment of alcohol use disorder: A critical review.
Front Pharmacol. 2022 Oct 3;13:927703. doi: 10.3389/fphar.2022.927703. eCollection 2022.
2
Pharmacogenetics of Addiction Therapy.
Methods Mol Biol. 2022;2547:437-490. doi: 10.1007/978-1-0716-2573-6_16.
3
On the path towards personalized medicine: Implications of pharmacogenetic studies of alcohol use disorder medications.
Expert Rev Precis Med Drug Dev. 2020;5(1):43-54. doi: 10.1080/23808993.2020.1724510. Epub 2020 Feb 10.
4
Mechanisms of Shared Vulnerability to Post-traumatic Stress Disorder and Substance Use Disorders.
Front Behav Neurosci. 2020 Jan 31;14:6. doi: 10.3389/fnbeh.2020.00006. eCollection 2020.
5
Antidepressants for the treatment of people with co-occurring depression and alcohol dependence.
Cochrane Database Syst Rev. 2018 Apr 24;4(4):CD008581. doi: 10.1002/14651858.CD008581.pub2.
6
Combined Effects of Acamprosate and Escitalopram on Ethanol Consumption in Mice.
Alcohol Clin Exp Res. 2016 Jul;40(7):1531-9. doi: 10.1111/acer.13099. Epub 2016 May 17.
7
Critical needs in drug discovery for cessation of alcohol and nicotine polysubstance abuse.
Prog Neuropsychopharmacol Biol Psychiatry. 2016 Feb 4;65:269-87. doi: 10.1016/j.pnpbp.2015.11.004. Epub 2015 Nov 12.
8
Serotonergic gene variation in substance use pharmacotherapy: a systematic review.
Pharmacogenomics. 2015;16(11):1307-14. doi: 10.2217/pgs.15.72. Epub 2015 Aug 12.
9
Serotonergic Systems in the Pathophysiology of Ethanol Dependence: Relevance to Clinical Alcoholism.
ACS Chem Neurosci. 2015 Jul 15;6(7):1026-39. doi: 10.1021/cn5003573. Epub 2015 Feb 19.
10
Combining seeking safety with sertraline for PTSD and alcohol use disorders: A randomized controlled trial.
J Consult Clin Psychol. 2015 Apr;83(2):359-69. doi: 10.1037/a0038719. Epub 2015 Jan 26.

本文引用的文献

1
Comparison of alcoholism subtypes as moderators of the response to sertraline treatment.
Alcohol Clin Exp Res. 2012 Mar;36(3):509-16. doi: 10.1111/j.1530-0277.2011.01609.x. Epub 2011 Sep 6.
3
The impact of analytic method on interpretation of outcomes in longitudinal clinical trials.
Int J Clin Pract. 2008 Aug;62(8):1147-58. doi: 10.1111/j.1742-1241.2008.01808.x. Epub 2008 Jun 28.
4
Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder.
Am J Hum Genet. 2006 May;78(5):815-826. doi: 10.1086/503850. Epub 2006 Mar 28.
5
An expanded evaluation of the relationship of four alleles to the level of response to alcohol and the alcoholism risk.
Alcohol Clin Exp Res. 2005 Jan;29(1):8-16. doi: 10.1097/01.alc.0000150008.68473.62.
6
Treatment outcomes in type A and B alcohol dependence 6 months after serotonergic pharmacotherapy.
Alcohol Clin Exp Res. 2004 Jul;28(7):1065-73. doi: 10.1097/01.alc.0000130974.50563.04.
7
Using daily interactive voice response technology to measure drinking and related behaviors in a pharmacotherapy study.
Alcohol Clin Exp Res. 2004 Jul;28(7):1060-4. doi: 10.1097/01.alc.0000130806.12066.9c.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验