Subhani Mohsan, Dhanda Ashwin, King James A, Warren Fiona C, Creanor Siobhan, Davies Melanie J, Eldeghaidy Sally, Bawden Stephen, Gowland Penny A, Bataller Ramon, Greenwood Justin, Kaar Stephen, Bhala Neeraj, Aithal Guruprasad P
Nottingham Digestive Diseases Centre (NDDC), Translational Medical Sciences, School of Medicine, University of Nottingham, NG7 2UH, UK.
NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham NG7 2UH, UK.
EClinicalMedicine. 2024 Nov 14;78:102920. doi: 10.1016/j.eclinm.2024.102920. eCollection 2024 Dec.
Despite the availability of various pharmacological and behavioural interventions, alcohol-related mortality is rising. This systematic review aimed to critically evaluate the existing literature on the association between glucagon-like peptide-1 receptor agonists use (GLP-1 RAs) and alcohol consumption.
Electronic searches were conducted on Ovid Medline, EMBASE, PsycINFO, clintrials.gov, and ProQuest until the end of March 2024. An updated search was done on 7th of August 2024. The primary outcome was to explore the association between GLP-1 RAs use and change in alcohol consumption. Secondary outcomes included evaluating the impact of GLP-1 RAs on occurrences of alcohol-related events, healthcare utilisation, and the effect on functional magnetic resonance imaging (fMRI) cue reactivity. This study is registered with PROSPERO #CRD42024531982.
Six studies totalling 88,190 participants were included with 38,740 (43.9%) receiving GLP-1 RA, but only 286 participated in randomised controlled trials. Pooled mean age was 49.6 years (SD = 10.5). RCT data did not show a reduction in alcohol consumption over 30 days after 24 weeks of treatment with exenatide versus placebo (heavy drinking days 6.0 [higher in control group], 95% CI -7.4 to 19.4, p = 0.37), a subgroup analysis found a positive effect in people with obesity (BMI >30 kg/m), with significant reductions in brain reward centre cue reactivity on fMRI. In a secondary analysis of an RCT participants taking dulaglutide compared to placebo were 29% more likely to reduce alcohol intake (relative effect size 0.71, 95% CI 0.52-0.97, p = 0.04). Observational studies showed fewer alcohol-related healthcare events and a significant reduction in alcohol use with GLP-1 RAs treatment compared to DPP4-Dipeptidyl peptidase 4 use, no treatment and/or alcohol intake at baseline.
There is little high-quality evidence demonstrating the effect of GLP-1 RAs on alcohol use. Subgroup analysis from two RCTs and supporting data from four observational studies suggest that GLP-1 RAs may reduce alcohol consumption and improve outcomes in some individuals. Heterogeneous study findings warrant further research to establish the effectiveness and safety of GLP-1 RAs in this population.
National Institute for Health and Care Research (NIHR): Award-ID: NIHR155469; NIHR154191; NIHR155530. NIHR Nottingham Biomedical Research Centre, Award-ID: BRC-1215-20003.
尽管有各种药物和行为干预措施,但与酒精相关的死亡率仍在上升。本系统评价旨在严格评估关于胰高血糖素样肽-1受体激动剂(GLP-1 RAs)使用与饮酒之间关联的现有文献。
在Ovid Medline、EMBASE、PsycINFO、clintrials.gov和ProQuest上进行电子检索,直至2024年3月底。2024年8月7日进行了更新检索。主要结局是探讨GLP-1 RAs使用与饮酒变化之间的关联。次要结局包括评估GLP-1 RAs对酒精相关事件发生、医疗保健利用的影响,以及对功能磁共振成像(fMRI)线索反应性的影响。本研究已在PROSPERO注册,注册号为#CRD42024531982。
纳入了6项研究,共计88,190名参与者,其中38,740名(43.9%)接受GLP-1 RA治疗,但只有286名参与了随机对照试验。合并平均年龄为49.6岁(标准差 = 10.5)。随机对照试验数据显示,与安慰剂相比,艾塞那肽治疗24周后30天内饮酒量没有减少(重度饮酒天数6.0 [对照组较高],95%置信区间 -7.4至19.4,p = 0.37),亚组分析发现肥胖者(体重指数>30 kg/m²)有积极效果,fMRI显示脑奖赏中枢线索反应性显著降低。在一项随机对照试验的二次分析中,与安慰剂相比,服用度拉鲁肽的参与者减少酒精摄入量的可能性高29%(相对效应大小0.71,95%置信区间0.52 - 0.97,p = 0.04)。观察性研究显示,与使用二肽基肽酶4(DPP4)、未治疗和/或基线时饮酒相比,GLP-1 RAs治疗的酒精相关医疗事件较少,酒精使用显著减少。
几乎没有高质量证据证明GLP-1 RAs对饮酒的影响。两项随机对照试验的亚组分析和四项观察性研究的支持数据表明,GLP-1 RAs可能会减少某些个体的酒精消费并改善结局。研究结果的异质性值得进一步研究,以确定GLP-1 RAs在该人群中的有效性和安全性。
国家卫生与保健研究机构(NIHR):资助编号:NIHR155469;NIHR154191;NIHR155530。NIHR诺丁汉生物医学研究中心,资助编号:BRC-1215-20003。