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GLP-1R 激动剂艾塞那肽治疗可卡因使用障碍的可行性:一项病例系列研究。

Feasibility of Exenatide, a GLP-1R Agonist, for Treating Cocaine Use Disorder: A Case Series Study.

机构信息

From the University of Texas Health Science Center at Houston, Houston, TX.

出版信息

J Addict Med. 2023;17(4):481-484. doi: 10.1097/ADM.0000000000001147. Epub 2023 Feb 17.

Abstract

Cocaine use remains a serious public health problem associated with a marked increase in overdose deaths in the past decade. No medications have yet been proven to be effective for the treatment of cocaine use disorder (CUD). Among the highly promising medications have been glucagon-like peptide 1 receptor agonists (GLP-1RA) that are currently used for the treatment of type 2 diabetes mellitus and weight management. Preclinically, GLP-1RAs have been shown to attenuate cocaine self-administration, however, this has not yet been demonstrated in a human laboratory study. The GLP-1RA extended-release exenatide is given as a once-weekly injection, which may be clinically advantageous for addressing medication nonadherence among individuals with CUD. Here, we assess feasibility and safety by reporting on 3 cases of patients with CUD who received 6 weeks of exenatide 2 mg subcutaneously once-weekly in an open-label fashion, along with standard individual drug counseling. We observed excellent attendance and compliance, along with positive end-of-study satisfaction ratings. The medication was well tolerated and without unexpected or severe adverse events. Results for cocaine use and related clinical effects were more mixed, yet encouraging. Future empirical testing of exenatide for treating CUD should utilize a randomized controlled trial design and longer treatment duration.

摘要

可卡因的使用仍然是一个严重的公共卫生问题,在过去十年中,与可卡因相关的过量死亡人数显著增加。目前还没有药物被证明对可卡因使用障碍(CUD)的治疗有效。有前景的药物之一是胰高血糖素样肽 1 受体激动剂(GLP-1RA),目前用于治疗 2 型糖尿病和体重管理。在临床前研究中,GLP-1RAs 已被证明可以减轻可卡因的自我给药,但这尚未在人类实验室研究中得到证实。GLP-1RA 延长释放艾塞那肽每周注射一次,这可能对解决 CUD 患者的药物不依从性具有临床优势。在这里,我们通过报告 3 例接受每周一次皮下注射 2 毫克艾塞那肽 6 周的 CUD 患者的情况,评估了该方法的可行性和安全性,同时还进行了标准的个体药物咨询。我们观察到了极好的出勤率和依从性,以及研究结束时的满意度评分较高。该药物耐受性良好,没有出现意外或严重的不良事件。可卡因使用和相关临床效果的结果则更为复杂,但仍令人鼓舞。未来对艾塞那肽治疗 CUD 的实证检验应采用随机对照试验设计和更长的治疗时间。

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