Kellner David A, Dente Elizabeth, Tran Vincent, Welsh Travis, Tran Victor, Saha Angshuman, Baker Joshua F, Elashoff David A, Ranganath Veena K
David Geffen School of Medicine, University of California, Los Angeles.
Perelman School of Medicine, University of Pennsylvania and Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia.
ACR Open Rheumatol. 2025 Sep;7(9):e70103. doi: 10.1002/acr2.70103.
Glucagon-like peptide 1 receptor agonists (GLP-1RAs) are approved for weight loss, diabetes, and cardiovascular risk reduction. Despite widespread use, GLP-1RAs have not been well studied in patients with rheumatoid arthritis (RA). We examined the effects of GLP-1RAs on RA disease activity and cardiovascular risk profile in patients with RA and overweight or obesity.
We conducted a retrospective chart review study of patients with RA with a body mass index of ≥27 who were prescribed a GLP-1RA (semaglutide or tirzepatide). Between 2018 and 2024, 173 patients with RA were identified in the treatment group (prescribed and took a GLP-1RA), and 42 patients with RA were identified in the control group (prescribed but did not take GLP-1RA). Patients were assessed at three-month intervals for up to one year after prescription. Outcome measures included RA disease activity, cardiovascular risk markers, and patient-reported outcomes. Changes in outcome measures within and between groups were assessed with linear mixed effect models, with adjustments for baseline characteristics that differed significantly between groups.
GLP-1RA-treated patients experienced significantly greater reductions in RA disease activity, pain, body weight, total cholesterol, and glycosylated hemoglobin than controls (P < 0.05). Within the treatment group, there were also significant reductions in erythrocyte sedimentation rate, C-reactive protein values, low-density lipoprotein cholesterol values, and triglyceride values (P < 0.05). Nearly one-third of the treatment group discontinued the GLP-1RA during the study period, with the most common adverse effect being gastrointestinal issues.
This study suggests that the use of GLP-1RAs can improve RA disease activity and cardiovascular risk profile. Although further research is needed, this novel finding has significant clinical implications because it suggests that anti-obesity medications may improve both cardiovascular and RA outcomes.
胰高血糖素样肽1受体激动剂(GLP-1RAs)已被批准用于减肥、治疗糖尿病和降低心血管疾病风险。尽管GLP-1RAs已被广泛使用,但在类风湿关节炎(RA)患者中尚未得到充分研究。我们研究了GLP-1RAs对RA患者且超重或肥胖患者的RA疾病活动度和心血管疾病风险状况的影响。
我们对体重指数≥27且被处方使用GLP-1RA(司美格鲁肽或替尔泊肽)的RA患者进行了一项回顾性病历审查研究。在2018年至2024年期间,治疗组(被处方并服用GLP-1RA)确定了173例RA患者,对照组(被处方但未服用GLP-1RA)确定了42例RA患者。在处方后长达一年的时间里,每隔三个月对患者进行评估。结果指标包括RA疾病活动度、心血管疾病风险标志物和患者报告的结果。使用线性混合效应模型评估组内和组间结果指标的变化,并对组间有显著差异的基线特征进行调整。
与对照组相比,接受GLP-1RA治疗的患者在RA疾病活动度、疼痛、体重、总胆固醇和糖化血红蛋白方面的降低幅度显著更大(P<0.05)。在治疗组内,红细胞沉降率、C反应蛋白值、低密度脂蛋白胆固醇值和甘油三酯值也有显著降低(P<0.05)。在研究期间,近三分之一的治疗组患者停用了GLP-1RA,最常见的不良反应是胃肠道问题。
本研究表明,使用GLP-1RAs可以改善RA疾病活动度和心血管疾病风险状况。尽管需要进一步研究,但这一新发现具有重要的临床意义,因为它表明抗肥胖药物可能改善心血管疾病和RA的治疗效果。