胰高血糖素样肽1受体激动剂对类风湿关节炎患者的影响。

IF 2.8 Q2 RHEUMATOLOGY
David A Kellner, Elizabeth Dente, Vincent Tran, Travis Welsh, Victor Tran, Angshuman Saha, Joshua F Baker, David A Elashoff, Veena K Ranganath
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引用次数: 0

摘要

目的:胰高血糖素样肽1受体激动剂(GLP-1RAs)被批准用于减肥、糖尿病和降低心血管风险。尽管被广泛使用,GLP-1RAs在类风湿关节炎(RA)患者中尚未得到很好的研究。我们研究了GLP-1RAs对RA和超重或肥胖患者的RA疾病活动性和心血管风险概况的影响。方法:我们对服用GLP-1RA(西马鲁肽或替西帕肽)的体重指数≥27的RA患者进行了回顾性图表回顾研究。2018年至2024年间,治疗组(处方并服用GLP-1RA)发现了173例RA患者,对照组(处方但未服用GLP-1RA)发现了42例RA患者。在处方后的一年内,每隔三个月对患者进行评估。结果测量包括类风湿性关节炎疾病活动性、心血管危险标志物和患者报告的结果。采用线性混合效应模型评估组内和组间结果测量的变化,并对组间差异显著的基线特征进行调整。结果:与对照组相比,glp - 1ra治疗的患者在RA疾病活动性、疼痛、体重、总胆固醇和糖化血红蛋白方面的降低明显更大(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显著降低(P < 0.05)。在研究期间,近三分之一的治疗组停止了GLP-1RA,最常见的不良反应是胃肠道问题。结论:本研究提示GLP-1RAs可改善RA疾病活动性和心血管风险。虽然还需要进一步的研究,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和类风湿性关节炎的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Glucagon-Like Peptide 1 Receptor Agonists on Patients With Rheumatoid Arthritis.

Objective: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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