重新利用SGLT-2抑制剂作为耐药梅尼埃病的新治疗策略

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Sun-Uk Lee, Euyhyun Park
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引用次数: 0

摘要

背景:梅尼埃氏病(MD)是一种慢性内耳疾病,影响约0.2%的人口,其中30%的患者对常规治疗仍然难治。病理生理学涉及内淋巴水肿,提示影响体液平衡的药物可能提供治疗益处。钠-葡萄糖共转运蛋白2 (SGLT-2)抑制剂,最初是为糖尿病开发的,提供独特的机制,包括钠尿和渗透性利尿,可能解决MD潜在的液体失衡。方法:我们在高丽大学安南医院进行了一项回顾性观察研究,分析了明确的MD患者(Bárány社会标准)的医疗记录,这些患者在2023年1月至2023年12月期间每天接受标签外用药恩格列净10mg。6例难治性MD患者(3男3女,平均年龄55.8岁)经常规治疗失败至少3个月。主要结局包括纯音阈值平均值(PTA)、低频阈值平均值(LFA)、眩晕发作频率和眩晕严重程度的变化,使用视觉模拟量表(VAS)评分,在基线和治疗3个月后进行评估。结果:所有患者均表现出听觉和前庭症状的临床显著改善。平均PTA由31.4 dB改善至20.8 dB(改善10.6 dB, p < 0.05)。低频听力恢复更为明显,LFA从37.2 dB改善至15.6 dB(改善21.6 dB, p < 0.01)。眩晕的频率从每月1.6次急剧下降到每月0.1次,有4名患者经历了眩晕发作的完全缓解。眩晕严重程度的VAS评分从5.2降至0.5。治疗耐受性良好,仅有2例患者报告了轻微的不良反应:1例患者出现短暂性多尿,另1例患者体重减轻5公斤,这与已知的SGLT-2抑制剂的药理学特征一致。结论:这项初步研究表明,重新使用SGLT-2抑制剂治疗耐药MD具有潜在的临床益处。然而,回顾性设计和固有局限性阻碍了对因果关系的明确结论。在听力阈值和前庭症状方面观察到的显着改善值得通过随机对照试验进行进一步调查,并采用客观结果测量来确定这种治疗方法的真正疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repurposing SGLT-2 Inhibitors as a Novel Therapeutic Strategy for Treatment-Resistant Meniere's Disease.

Background: Meniere's disease (MD) is a chronic inner ear disorder affecting approximately 0.2% of the population, with 30% of patients remaining refractory to conventional treatments. The pathophysiology involves endolymphatic hydrops, suggesting that agents affecting fluid homeostasis might provide therapeutic benefit. Sodium-glucose cotransporter 2 (SGLT-2) inhibitors, originally developed for diabetes, offer unique mechanisms including natriuresis and osmotic diuresis that may address the underlying fluid imbalance in MD. Methods: We conducted a retrospective observational study at the Korea University Anam Hospital, analyzing the medical records of patients with definite MD (Bárány Society criteria) who received off-label empagliflozin 10 mg daily between January 2023 and December 2023. Six patients (3 men, 3 women; mean age 55.8 years) with treatment-resistant MD were identified who had failed conventional therapy for at least 3 months. Primary outcomes included changes in pure tone threshold average (PTA), low-frequency threshold average (LFA), vertigo episode frequency, and vertigo severity using visual analog scale (VAS) scores, assessed at baseline and after 3 months of treatment. Results: All patients demonstrated clinically significant improvements in both auditory and vestibular symptoms. Mean PTA improved from 31.4 dB to 20.8 dB (improvement of 10.6 dB, p < 0.05). Low-frequency hearing showed more substantial recovery, with LFA improving from 37.2 dB to 15.6 dB (improvement of 21.6 dB, p < 0.01). Vertigo frequency decreased dramatically from 1.6 episodes per month to 0.1 episodes per month, with four patients experiencing a complete resolution of vertigo episodes. VAS scores for vertigo severity decreased from 5.2 to 0.5. Treatment was well-tolerated, with only minor adverse effects reported in two patients: transient polyuria in one patient and 5 kg weight loss in another, both consistent with the known pharmacological profile of SGLT-2 inhibitors. Conclusions: This preliminary study suggests a potential clinical benefit of repurposing SGLT-2 inhibitors for treatment-resistant MD. However, the retrospective design and inherent limitations prevent definitive conclusions about causality. The significant improvements observed in both hearing thresholds and vestibular symptoms warrant further investigation through randomized controlled trials with objective outcome measures to establish the true efficacy of this therapeutic approach.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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