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以白质神经保护为靶点,预防可卡因使用障碍复发的治疗策略:一项以机制为重点的随机临床试验设计。

Targeting white matter neuroprotection as a relapse prevention strategy for treatment of cocaine use disorder: Design of a mechanism-focused randomized clinical trial.

机构信息

Faillace Department of Psychiatry and Behavioral Sciences, McGovern Medical School, University of Texas Health Science Center at Houston, USA.

Faillace Department of Psychiatry and Behavioral Sciences, McGovern Medical School, University of Texas Health Science Center at Houston, USA.

出版信息

Contemp Clin Trials. 2021 Dec;111:106603. doi: 10.1016/j.cct.2021.106603. Epub 2021 Oct 22.

Abstract

Cocaine use continues to be a significant public health problem with limited treatment options and no approved pharmacotherapies. Cognitive-behavioral therapy (CBT) remains the mainstay treatment for preventing relapse, however, people with chronic cocaine use display cognitive impairments that are associated with poor response to CBT. Emerging evidence in animal and human studies suggests that the peroxisome proliferator-activated receptor-gamma (PPAR- γ) agonist, pioglitazone, improves white matter integrity that is essential for cognitive function. This project will determine whether adjunctive use of pioglitazone enhances the effect of CBT in preventing relapse during the early phase of recovery from cocaine use disorder. This paper describes the design of a mechanism-focused phase 2 randomized clinical trial that aims first to evaluate the effects of pioglitazone on targeted mechanisms related to white matter integrity, cognitive function, and cocaine craving; and second, to evaluate the extent to which improvements on target mechanisms predict CBT response. Positive results will support pioglitazone as a potential cognitive enhancing agent to advance to later stage medication development research.

摘要

可卡因的使用仍然是一个严重的公共卫生问题,治疗选择有限,且没有经过批准的药物治疗。认知行为疗法(CBT)仍然是预防复发的主要治疗方法,然而,慢性可卡因使用者表现出的认知障碍与对 CBT 的反应不佳有关。动物和人类研究中的新证据表明,过氧化物酶体增殖物激活受体-γ(PPAR-γ)激动剂吡格列酮可改善对认知功能至关重要的白质完整性。该项目将确定辅助使用吡格列酮是否能增强 CBT 在可卡因使用障碍康复早期预防复发的效果。本文描述了一项以机制为重点的 2 期随机临床试验的设计,该试验旨在首先评估吡格列酮对与白质完整性、认知功能和可卡因渴求相关的靶向机制的影响;其次,评估目标机制的改善程度是否能预测 CBT 的反应。积极的结果将支持吡格列酮作为一种潜在的认知增强剂,推进到后期药物开发研究。

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