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高剂量纳曲酮治疗可卡因和酒精依赖时治疗中断预测因素的性别差异。

Gender differences in predictors of treatment attrition with high dose naltrexone in cocaine and alcohol dependence.

作者信息

Suh Jesse J, Pettinati Helen M, Kampman Kyle M, O'Brien Charles P

机构信息

Center for Studies of Addiction, Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA. Suh

出版信息

Am J Addict. 2008 Nov-Dec;17(6):463-8. doi: 10.1080/10550490802409074.

DOI:10.1080/10550490802409074
PMID:19034737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2657877/
Abstract

Recently, we reported that naltrexone at 150 mg/day significantly decreased cocaine and alcohol use for men but not women with co-occurring cocaine and alcohol dependence. The present study is an exploratory investigation of predictors that explain the different gender responses to naltrexone, with a particular focus on differential predictors of treatment attrition. No significant predictors were associated with treatment discontinuation in men. Women, however, were more likely to discontinue treatment when reporting severe pre-treatment psychiatric problems or nausea while in treatment. Further research on the impact of pre-treatment and in-treatment gender differences with naltrexone is warranted.

摘要

最近,我们报告称,对于同时患有可卡因和酒精依赖的男性,每天服用150毫克纳曲酮可显著减少其可卡因和酒精的使用,但对女性则无此效果。本研究是一项探索性调查,旨在探究能够解释纳曲酮对不同性别产生不同反应的预测因素,特别关注治疗中断的差异预测因素。在男性中,没有显著的预测因素与治疗中断相关。然而,女性在报告有严重的治疗前精神问题或治疗期间出现恶心时,更有可能中断治疗。有必要进一步研究治疗前和治疗期间性别差异对纳曲酮疗效的影响。

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本文引用的文献

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An evaluation of mu-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence: results from the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study.评估μ-阿片受体(OPRM1)作为纳曲酮治疗酒精依赖反应预测指标的研究:酒精依赖联合药物治疗与行为干预(COMBINE)研究结果
Arch Gen Psychiatry. 2008 Feb;65(2):135-44. doi: 10.1001/archpsyc.65.2.135.
2
Prospects for a genomic approach to the treatment of alcoholism.采用基因组方法治疗酒精中毒的前景。
Arch Gen Psychiatry. 2008 Feb;65(2):132-3. doi: 10.1001/archgenpsychiatry.2007.32.
3
Gender differences with high-dose naltrexone in patients with co-occurring cocaine and alcohol dependence.高剂量纳曲酮在同时患有可卡因和酒精依赖患者中的性别差异。
J Subst Abuse Treat. 2008 Jun;34(4):378-90. doi: 10.1016/j.jsat.2007.05.011. Epub 2007 Jul 30.
4
Association of a functional polymorphism in the mu-opioid receptor gene with alcohol response and consumption in male rhesus macaques.恒河猴μ-阿片受体基因功能性多态性与酒精反应及酒精摄入量的关联
Arch Gen Psychiatry. 2007 Mar;64(3):369-76. doi: 10.1001/archpsyc.64.3.369.
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Targeting treatments for alcohol dependence: the pharmacogenetics of naltrexone.酒精依赖的靶向治疗:纳曲酮的药物遗传学
Addict Biol. 2006 Sep;11(3-4):397-403. doi: 10.1111/j.1369-1600.2006.00036.x.
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J Stud Alcohol Suppl. 2005 Jul(15):170-8; discussion 168-9. doi: 10.15288/jsas.2005.s15.170.
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