胰高血糖素样肽-1激动剂对膀胱过动症患者的影响:一项初步研究

Max D. Sandler , Adam D. Williams , Alan Wein , Katherine Amin , Raveen Syan
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引用次数: 0

摘要

目的:探讨胰高血糖素样肽-1 (GLP-1)激动剂(通常用于糖尿病和肥胖症)对膀胱过动症(OAB)症状主观影响的初步数据,以指导未来更大规模的研究。方法:我们在网上论坛上进行匿名调查。使用GLP-1激动剂并经历OAB症状的18岁或以上的参与者符合条件。我们收集了受试者OAB症状、体重变化、GLP-1处方原因和人口统计数据。数据分析采用SAS®软件,显著性设置为p <;0.05.结果:在33名受访者中,女性27人,男性6人。所有患者均使用西马鲁肽,主要用于减肥(96.9%)。除OAB外,还有4人患有泌尿系统疾病。11人(33.3%)报告在使用GLP-1激动剂后OAB症状改善,平均体重减轻12.2%,但这与症状没有改变或恶化的患者没有显著差异(分别平均体重减轻8.4%和10%;P = 0.24)。每天至少一次OAB发作的患者中,有一半的患者症状有所改善,而症状较少的患者中,这一比例为7.7% (p = 0.01)。在报告症状改善的参与者中,90.91%每天经历OAB (p = 0.01)。结论:虽然减肥可以改善OAB症状,但GLP-1激动剂的影响尚不清楚。我们的研究结果可能表明,基线时OAB症状更频繁的患者可能从GLP-1激动剂中获得更大的益处,为未来的研究提供了一个潜在的假设。需要进一步的研究来探讨这些药物如何影响OAB的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Glucagon like Peptide-1 agonists on patients with overactive bladder: A pilot study

Purpose:

To explore preliminary data on the subjective impact of Glucagon-Like Peptide-1 (GLP-1) agonists, commonly used for diabetes and obesity, on symptoms of overactive bladder (OAB), in order to guide future, larger-scale investigations.

Methods:

We distributed an anonymous survey on an online forum. Participants aged 18 or older who had used GLP-1 agonists and experienced OAB symptoms were eligible. We collected data on participants’ OAB symptoms, body weight changes, reasons for GLP-1 prescription, and demographics. Data was analyzed using SAS® software, with significance set at p < 0.05.

Results:

Of 33 respondents, 27 identified as female and 6 male. All used semaglutide, primarily for weight loss (96.9%). Four had a urinary condition besides OAB. Eleven (33.3%) reported OAB symptom improvement after starting GLP-1 agonists with mean weight loss of 12.2%, but this was not significantly different from those with no change or worsening symptoms (8.4% and 10% mean weight loss, respectively; p = 0.24). Half of those with OAB episodes at least once daily experienced symptom improvement, compared to 7.7% with less frequent symptoms (p = 0.01). Of participants reporting symptom improvement, 90.91% experienced OAB daily (p = 0.01).

Conclusion:

While weight loss can improve OAB symptoms, the impact of GLP-1 agonists remains unclear. Our findings may suggest that those with more frequent OAB symptoms at baseline may derive greater benefit from GLP-1 agonists, offering a potential hypothesis for future investigation. Further studies are needed to explore how these medications impact management of OAB.
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