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抗血管内皮生长因子治疗糖尿病性黄斑水肿。

Anti-VEGF therapy for diabetic macular edema.

机构信息

Department Of Ophthalmology, Mayo Clinic Florida, Jacksonville, FL, 32224, USA,

出版信息

Curr Diab Rep. 2014 Aug;14(8):510. doi: 10.1007/s11892-014-0510-4.

Abstract

Vascular endothelial growth factor (VEGF) plays a pivotal role in the development of diabetic macular edema (DME), the leading cause of vision loss among working-aged individuals. A decade of clinical trials demonstrated that drugs that bind soluble VEGF restore the integrity of the blood-retinal barrier, resolve macular edema, and improve vision in most patients with DME. Four drugs (pegaptanib, ranibizumab, bevacizumab, and aflibercept) effectively treat DME when administered by intravitreal injections. Only ranibizumab has received U.S. Food and Drug Administration (FDA) approval for DME, but bevacizumab is commonly used off-label, and an FDA application for aflibercept is pending. Effective treatment requires repeated injections, although recent data suggest that the treatment burden diminishes after 1 year. Intravitreal therapy is generally safe, although the incidence of systemic thromboembolic events varies among trials.

摘要

血管内皮生长因子 (VEGF) 在糖尿病性黄斑水肿 (DME) 的发展中起着关键作用,DME 是工作年龄段人群视力丧失的主要原因。十年来的临床试验表明,结合可溶性 VEGF 的药物可恢复血视网膜屏障的完整性,解决黄斑水肿,并改善大多数 DME 患者的视力。当通过玻璃体内注射给药时,四种药物(贝伐单抗、雷珠单抗、阿柏西普和康柏西普)可有效治疗 DME。只有雷珠单抗获得了美国食品和药物管理局 (FDA) 对 DME 的批准,但贝伐单抗通常被超适应证使用,阿柏西普的 FDA 申请正在等待中。有效的治疗需要反复注射,尽管最近的数据表明,治疗负担在 1 年后会减轻。玻璃体内治疗通常是安全的,尽管各试验中全身血栓栓塞事件的发生率有所不同。

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