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使用胰高血糖素样肽-1激动剂司美格鲁肽成功治疗暴饮暴食症:一项回顾性队列研究。

Successful treatment of binge eating disorder with the GLP-1 agonist semaglutide: A retrospective cohort study.

作者信息

Richards Jesse, Bang Neha, Ratliff Erin L, Paszkowiak Maria A, Khorgami Zhamak, Khalsa Sahib S, Simmons W Kyle

机构信息

Department of Internal Medicine, University of Oklahoma School of Community Medicine, Tulsa, OK, USA.

Department of Pharmacology & Physiology, Oklahoma State University, Center for Health Sciences, Tulsa, OK, USA.

出版信息

Obes Pillars. 2023 Jul 20;7:100080. doi: 10.1016/j.obpill.2023.100080. eCollection 2023 Sep.

Abstract

OBJECTIVE

Binge eating disorder (BED) is the most common eating disorder, and yet only one pharmacotherapy (lisdexamfetamine), which has known abuse-potential, is FDA-approved. Topiramate is also commonly prescribed off-label for binge eating but has many contraindications. In contrast, the glucagon-like peptide-1 (GLP1) analog semaglutide has profound effects on central satiety signaling leading to reduced food intake, and has been approved for the treatment of obesity based on its efficacy and safety profile. Semaglutide would thus seem to be a potential candidate for the treatment of BED.

METHODS

This open-label study examined the effects of semaglutide on Binge Eating Scale (BES) scores in individuals with BED. Patients were divided into three groups: those prescribed semaglutide, those prescribed either lisdexamphetamine or topiramate, and those prescribed a combination of semaglutide with lisdexamphetamine or topiramate.

RESULTS

Patients receiving semaglutide only exhibited greater reductions in BES scores compared to the other groups. Combined pharmacotherapy with both semaglutide and the other anti-obesity medications did not result in greater reductions in BES scores compared to the semaglutide-only group. Findings were similar in patients with moderate/severe BED, as well as the full sample.

CONCLUSION

The therapeutic effects of semaglutide in binge eating disorder warrant further investigation.

摘要

目的

暴饮暴食症(BED)是最常见的饮食失调症,但美国食品药品监督管理局(FDA)仅批准了一种有已知滥用潜力的药物疗法(赖右苯丙胺)。托吡酯也常用于暴饮暴食症的非标签处方治疗,但有许多禁忌症。相比之下,胰高血糖素样肽-1(GLP1)类似物司美格鲁肽对中枢饱腹感信号有深远影响,可导致食物摄入量减少,并且基于其疗效和安全性已被批准用于治疗肥胖症。因此,司美格鲁肽似乎是治疗暴饮暴食症的潜在候选药物。

方法

这项开放标签研究考察了司美格鲁肽对暴饮暴食症患者暴饮暴食量表(BES)评分的影响。患者被分为三组:接受司美格鲁肽治疗的患者、接受赖右苯丙胺或托吡酯治疗的患者,以及接受司美格鲁肽与赖右苯丙胺或托吡酯联合治疗的患者。

结果

与其他组相比,仅接受司美格鲁肽治疗的患者BES评分降低幅度更大。与仅使用司美格鲁肽的组相比,司美格鲁肽与其他抗肥胖药物联合药物治疗并未导致BES评分有更大幅度的降低。中度/重度暴饮暴食症患者以及整个样本中的结果相似。

结论

司美格鲁肽在暴饮暴食症中的治疗效果值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/10661993/34d9e6e10e95/gr1.jpg

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