Fralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA.
Graduate Program in Translational Biology, Medicine, and Health, Blacksburg, VA, USA.
Sci Rep. 2023 Nov 28;13(1):20998. doi: 10.1038/s41598-023-48267-2.
Alcohol Use Disorder (AUD) contributes significantly to global mortality. GLP-1 (Glucagon-like peptide-1) and GLP-1/GIP (Glucose-dependent Insulinotropic Polypeptide) agonists, FDA-approved for managing type 2 diabetes and obesity, where the former has shown to effectively reduce the consumption of alcohol in animal models but no reports exist on the latter. In this report, we conducted two studies. In the first study, we conducted an analysis of abundant social media texts. Specifically, a machine-learning based attribution mapping of ~ 68,250 posts related to GLP-1 or GLP-1/GIP agonists on the Reddit platform. Secondly, we recruited participants (n = 153; current alcohol drinkers; BMI ≥ 30) who self-reported either taking Semaglutide (GLP-1 agonist), Tirzepatide (the GLP-1/GIP combination) for ≥ 30 days or, as a control group; no medication to manage diabetes or weight loss for a within and between subject remote study. In the social media study, we report 8 major themes including effects of medications (30%); diabetes (21%); and Weight loss and obesity (19%). Among the alcohol-related posts (n = 1580), 71% were identified as craving reduction, decreased desire to drink, and other negative effects. In the remote study, we observe a significantly lower self-reported intake of alcohol, drinks per drinking episode, binge drinking odds, Alcohol Use Disorders Identification Test (AUDIT) scores, and stimulating, and sedative effects in the Semaglutide or Tirzepatide group when compared to prior to starting medication timepoint (within-subjects) and the control group (between-subjects). In summary, we provide initial real-world evidence of reduced alcohol consumption in people with obesity taking Semaglutide or Tirzepatide medications, suggesting potential efficacy for treatment in AUD comorbid with obesity.
酒精使用障碍(AUD)对全球死亡率有重大影响。GLP-1(胰高血糖素样肽-1)和 GLP-1/GIP(葡萄糖依赖性胰岛素释放多肽)激动剂已获得 FDA 批准用于治疗 2 型糖尿病和肥胖症,前者已被证明可有效减少动物模型中的酒精消耗,但后者尚无报道。在本报告中,我们进行了两项研究。第一项研究中,我们对丰富的社交媒体文本进行了分析。具体来说,我们对 Reddit 平台上与 GLP-1 或 GLP-1/GIP 激动剂相关的约 68250 个帖子进行了基于机器学习的归因映射。其次,我们招募了参与者(n=153;当前饮酒者;BMI≥30),他们自我报告至少服用了 Semaglutide(GLP-1 激动剂)、Tirzepatide(GLP-1/GIP 联合)30 天以上,或者作为对照组;没有药物来管理糖尿病或减肥,进行了一项在体和间体的远程研究。在社交媒体研究中,我们报告了 8 个主要主题,包括药物的影响(30%);糖尿病(21%);和减肥和肥胖(19%)。在与酒精相关的帖子(n=1580)中,71%被确定为减少渴望、减少饮酒欲望和其他负面影响。在远程研究中,与开始用药前时间点(在体)和对照组相比,我们观察到服用 Semaglutide 或 Tirzepatide 的参与者报告的酒精摄入量、每次饮酒的饮料量、狂饮几率、酒精使用障碍识别测试(AUDIT)评分以及兴奋剂和镇静剂效应均显著降低。总之,我们提供了肥胖人群服用 Semaglutide 或 Tirzepatide 药物可减少酒精消耗的初步真实世界证据,表明在 AUD 合并肥胖症的治疗中具有潜在疗效。