减肥和代谢手术前使用胰高血糖素样肽-1 受体激动剂的模式:一项多中心研究。

Shlomi Rayman, Evyatar Morduch, Anat Reiner-Benaim, Netta-Lee Catzman, Idan Carmeli, Dvir Froylich, David Goitein
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引用次数: 0

摘要

背景:胰高血糖素样肽-1 受体激动剂(G1RA)作为超重或肥胖患者的一种减肥治疗方法已越来越受欢迎,但其使用模式及其对代谢和减肥手术(MBS)候选者的影响仍未得到充分研究:目的:我们旨在调查代谢与减重手术候选者中使用过 G1RA 的患者的患病率、特征和结果:方法:回顾性收集以色列五家高容量 MBS 中心的数据:方法:回顾性收集 2023 年 2 月 1 日至 2023 年 9 月 30 日期间的数据。对人口统计学、临床和治疗数据进行分析,以评估 G1RA 使用史、相关因素、不良事件和治疗结果:研究共纳入了 434 名 MBS 候选人。275名(63%)MBS候选者有使用G1RA的历史,其中利拉鲁肽和赛马鲁肽是最常用的药物。年龄较小、2 型糖尿病、血脂异常以及既往无 MBS 病史者使用 G1RA 的比例较高。这些药物的最大减重中位数为 5.38 千克,平均用药时间为 19 周。与使用时间较短的患者相比,使用 G1RA≥6 周的患者体重减轻幅度明显更大(6.3 ± 6.43 vs 1.65 ± 1.69;P < .001)。57.8%的患者出现了消化道相关不良事件。超过 95% 的患者因体重减轻不足和/或不良反应而停用 G1RA。利拉鲁肽(5.9 ± 4.98 kg vs. 3.9 ± 5.53 kg; P = .03)和塞马鲁肽(6.5 ± 7.8 kg vs. 2.5 ± 3.8 kg; P = .016)达到最大推荐剂量的患者与未达到最大推荐剂量的患者相比,体重减轻幅度明显更大:结论:在 MBS 候选者中,MBS 前 G1RA 利用率和失败率很高。我们的研究强调了进一步研究的必要性,以了解 G1RA 治疗在肥胖管理中的作用,并为在 MBS 候选者中适当使用 G1RA 制定指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utilization patterns of glucagon like Peptide-1 receptor agonists prior to bariatric and metabolic surgery: a multicenter study.

Background: Glucagon-like-peptide-1 receptor agonists (G1RA) have gained popularity as a treatment for weight loss in patients who are overweight or obese, but their utilization patterns and impact on candidates for metabolic and bariatric surgery (MBS) remain understudied.

Objective: We aimed to investigate the prevalence, characteristics, and outcomes of patients with a history of G1RA utilization among MBS candidates.

Setting: Five high-volume MBS centers in Israel.

Methods: Data were collected retrospectively from February 1st, 2023, to September 30th, 2023. Demographic, clinical, and treatment data were analyzed to assess a history of G1RA use, associated factors, adverse events, and treatment outcomes.

Results: Four hundred thirty-four MBS candidates were included in the study. A history of G1RA utilization was obtained in 275 (63%) MBS candidates, with Liraglutide and Semaglutide being the most commonly used agents. Younger age, type 2 diabetes mellitus, dyslipidemia, and no previous MBS history were associated with a higher rate of G1RA utilization. With these medications, median maximal weight loss was 5.38 kg, and mean duration of use was 19 weeks. Patients using G1RA for ≥6 weeks experienced significantly greater weight loss compared to those using it for shorter periods (6.3 ± 6.43 vs 1.65 ± 1.69; P < .001). GI-related adverse events were reported in 57.8% of patients. Over 95% of patients discontinued G1RA due to insufficient weight loss and/or adverse effects. Patients reaching the maximal recommended dose exhibited significantly greater weight loss versus patients who did not reach it for both Liraglutide (5.9 ± 4.98 kg vs. 3.9 ± 5.53 kg; P = .03) and Semaglutide (6.5 ± 7.8 kg vs. 2.5 ± 3.8 kg; P = .016).

Conclusion: Pre-MBS G1RA utilization and failure are prevalent among MBS candidates. Our study underscores the need for further research to understand the role of G1RA therapy in obesity management and the development of guidelines for its appropriate use in MBS candidates.

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