Aganirsen作为调节角膜新生血管的治疗选择:一个真实世界的病例系列研究。

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-09-22 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S545516
Salvador García-Delpech, Sara Fathi Nieto, Ana Hervás Ontiveros, Patricia Udaondo, Damian Garcia-Teillard
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引用次数: 0

摘要

目的:评估aganirsen(一种靶向胰岛素受体底物-1 (IRS-1)的反义寡核苷酸)在角膜移植患者中减少角膜新生血管(CoNV)的临床疗效。患者和方法:回顾性队列研究:术前1周和术后至少3个月每日2次给予阿格尼森1滴(0.86 mg/mL)治疗的患者。用裂隙灯检查定性评价新生血管的变化。结果:纳入研究人群65例(男性61.5%),平均年龄60.3岁。仅1例(1.5%)出现双侧CoNV。主要诊断为角膜营养不良占61.5%,移植排斥反应占10.8%,单纯疱疹性角膜炎和白血病各占7.7%,机械性创伤占3.1%。治疗3个月后,观察到所有眼睛新生血管的减少(100%)。结果不受人口统计学特征或诊断的影响。65例患者中有3例(4.6%)使用aganirsen治疗后无需进行移植物手术。62例患者中有5例角膜移植失败(8.1%)。5例患者就诊时诊断为角膜营养不良2例,既往移植排斥2例,疱疹性角膜原膜炎1例。一些患者出现轻微的结膜充血,1例患者出现瘙痒,并在治疗2个月时停止研究。结论:这项在移植手术前1周开始使用阿格尼森数月的现实世界研究增加了该药物在调节新血管形成方面的临床益处的证据。规范和延长阿格尼森治疗时间可以进一步优化角膜移植的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aganirsen as a Therapeutic Alternative for Modulating Corneal Neovascularization: A Real-World Case Series Study.

Purpose: To assess the clinical benefits of aganirsen, an antisense oligonucleotide targeting insulin receptor substrate-1 (IRS-1), for reducing corneal neovascularization (CoNV) in patients scheduled for corneal transplantation.

Patients and methods: Retrospective cohort study of patients who were treated with 1 drop of aganirsen (0.86 mg/mL) twice daily during 1 week preoperatively and at least 3 months after surgery. Changes in neovascularization were assessed qualitatively on slit-lamp examination.

Results: The study population included 65 patients (males 61.5%), with a mean age of 60.3 years. Bilateral CoNV was observed in 1 patient only (1.5%). Main diagnoses included corneal dystrophy in 61.5% of patients, transplant rejection in 10.8%, herpes simplex keratitis and leucoma in 7.7% each, and mechanical trauma in 3.1%. A reduction of neovascularization was observed in all eyes (100%) after 3 months of treatment. Results were not influenced by demographic characteristics or diagnosis. Treatment with aganirsen made graft surgery unnecessary in 3 out of 65 patients (4.6%). Failure of corneal transplantation occurred in 5 out of 62 patients (8.1%). Diagnosis at presentation in these 5 patients were corneal dystrophy in 2, previous transplant rejection in 2, and herpetic keratouveitis in 1. Some patients presented minor conjunctival hyperemia, and 1 patient reported pruritus and discontinued the study at 2 months of treatment.

Conclusion: This real-world study of the use of aganirsen months starting 1 week before graft surgery adds evidence of the clinical benefits of this agent in modulating neovascularization. Standardizing and extending the duration of treatment with aganirsen may further optimize the outcome of corneal transplantation.

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