Pierret Aureliane C S, Mizuno Yuya, Saunders Pippa, Lim Eshaya, De Giorgi Riccardo, Howes Oliver D, McCutcheon Robert A, McGowan Barbara, Sen Gupta Piya, Smith Daniel, Ismail Khalida, Pillinger Toby
Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, United Kingdom.
JAMA Psychiatry. 2025 May 14. doi: 10.1001/jamapsychiatry.2025.0679.
People with obesity and diabetes have poorer psychiatric and cognitive outcomes and lower quality of life (QOL) compared with those without. Glucagon-like peptide 1 receptor agonists (GLP1-RAs) are treatments for diabetes and obesity that may also influence psychiatric outcomes.
To conduct a meta-analysis of randomized placebo-controlled trials to evaluate psychiatric, cognitive, and QOL outcomes with GLP1-RA treatment.
MEDLINE, Embase, PsycINFO, and CENTRAL databases were searched from inception through June 24, 2024.
Double-blind placebo-controlled trials comparing GLP1-RA to placebo in adults with overweight/obesity and/or diabetes, reporting on psychiatric, cognition, or QOL outcomes, were included.
Data extraction was performed in parallel by 2 reviewers. Random-effects meta-analysis was performed. Effect size measures were log risk ratios (log[RR]) and standardized mean differences (Hedges g). The quality of studies was appraised using the Cochrane risk-of-bias tool (RoB2). Certainty of evidence was assessed via GRADEpro.
Main outcomes were risk of psychiatric adverse events (serious and nonserious) and change in mental health symptom severity, health-related quality of life, and cognition.
Eighty randomized clinical trials involving 107 860 patients were included in the meta-analysis. The mean (SD) age of participants across studies in the meta-analysis was 60.1 (7.1) years; 43 251 were female (40.1%) and 64 608 male (59.9%). GLP1-RA treatment was not associated with a significant difference in risk of serious psychiatric adverse events (log[RR] = -0.02; 95% CI, -0.20 to 0.17; P = .87) and nonserious psychiatric adverse events (log[RR] = -0.03; 95% CI, -0.21 to 0.16], P = .76), or depressive symptom change (g = 0.02; 95% CI, -0.51 to 0.55; P = .94), compared with placebo. GLP1-RA treatment was associated with improvements in restrained eating (g = 0.35; 95% CI, 0.13 to 0.57; P = .002) and emotional eating behavior (g = 0.32; 95% CI, 0.11 to 0.54; P = .003) and in mental health-related QOL (g = 0.15; 95% CI, 0.07 to 0.22; P < .001), physical health-related QOL (g = 0.20; 95% CI, 0.14 to 0.26; P < .001), diabetes-related QOL (g = 0.23; 95% CI, 0.15 to 0.32; P < .001), and weight-related QOL (g = 0.27; 95% CI, 0.18 to 0.35; P < .001) compared with placebo.
In patients with overweight/obesity and/or diabetes , GLP1-RA treatment is not associated with increased risk of psychiatric adverse events or worsening depressive symptoms relative to placebo and is associated with improvements in QOL, restrained eating, and emotional eating behavior. These findings provide reassurance regarding the psychiatric safety profile of GLP1-RAs and suggest that GLP1-RA treatment contributes to both physical and emotional well-being.
与非肥胖和糖尿病患者相比,肥胖和糖尿病患者的精神和认知结局较差,生活质量(QOL)较低。胰高血糖素样肽1受体激动剂(GLP1-RAs)是治疗糖尿病和肥胖症的药物,也可能影响精神结局。
进行一项随机安慰剂对照试验的荟萃分析,以评估GLP1-RA治疗的精神、认知和QOL结局。
从数据库建立至2024年6月24日,检索MEDLINE、Embase、PsycINFO和CENTRAL数据库。
纳入在超重/肥胖和/或糖尿病成人中比较GLP1-RA与安慰剂的双盲安慰剂对照试验,报告精神、认知或QOL结局。
由2名审阅者并行进行数据提取。进行随机效应荟萃分析。效应量测量为对数风险比(log[RR])和标准化均数差(Hedges g)。使用Cochrane偏倚风险工具(RoB2)评估研究质量。通过GRADEpro评估证据的确定性。
主要结局为精神不良事件(严重和非严重)的风险以及心理健康症状严重程度、健康相关生活质量和认知的变化。
荟萃分析纳入了80项涉及107 860名患者的随机临床试验。荟萃分析中各研究参与者的平均(标准差)年龄为60.1(7.1)岁;43 251名女性(40.1%),64 608名男性(59.9%)。与安慰剂相比,GLP1-RA治疗在严重精神不良事件风险(log[RR] = -0.02;95%CI,-0.20至0.17;P = 0.87)、非严重精神不良事件风险(log[RR] = -0.03;95%CI,-0.21至0.16;P = 0.76)或抑郁症状变化(g = 0.02;95%CI,-0.51至0.55;P = 0.94)方面无显著差异。与安慰剂相比,GLP1-RA治疗与节制饮食(g = 0.35;95%CI,0.13至0.57;P = 0.002)、情绪化饮食行为(g = 0.32;95%CI,0.11至0.54;P = 0.003)、心理健康相关QOL(g = 0.15;95%CI,0.07至0.22;P < 0.001)、身体健康相关QOL(g = 0.20;95%CI,0.14至0.26;P < 0.001)、糖尿病相关QOL(g = 0.23;95%CI,0.15至0.32;P < 0.001)和体重相关QOL(g = 0.27;95%CI,0.18至0.35;P < 0.001)的改善相关。
在超重/肥胖和/或糖尿病患者中,与安慰剂相比,GLP1-RA治疗与精神不良事件风险增加或抑郁症状恶化无关,且与QOL、节制饮食和情绪化饮食行为的改善相关。这些发现为GLP1-RAs的精神安全性提供了保证,并表明GLP1-RA治疗有助于身心健康。