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湿性年龄相关性黄斑变性患者接受抗血管内皮生长因子治疗后黄斑萎缩的发展。

Development of Macular Atrophy in Patients with Wet Age-Related Macular Degeneration Receiving Anti-VEGF Treatment.

机构信息

University of Nottingham Medical School, Queen's Medical Centre, Nottingham, United Kingdom.

Department of Ophthalmology, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Ophthalmologica. 2022;245(3):204-217. doi: 10.1159/000520171. Epub 2021 Oct 25.

Abstract

Age-related macular degeneration (AMD) is a leading cause of blindness. Late AMD can be classified into exudative (commonly known as wet AMD [wAMD]) or dry AMD, both of which may progress to macular atrophy (MA). MA causes irreversible vision loss and currently has no approved pharmacological treatment. The standard of care for wAMD is treatment with anti-vascular endothelial growth factors (VEGFs). However, recent evidence suggests that anti-VEGF treatment may play a role in the development of MA. Therefore, it is important to identify risk factors for the development of MA in patients with wAMD. For example, excessive blockade of VEGF through intense use of anti-VEGF agents may accelerate the development of MA. Patients with type III macular neovascularization (retinal angiomatous proliferation) have a particularly high risk of MA. These patients are characterized as having a pre-existing thin choroid (age-related choroidopathy), suggesting that the choroidal circulation is unable to respond to increased VEGF expression. Evidence suggests that subretinal fluid (possibly indicative of residual VEGF activity) may play a protective role. Patients receiving anti-VEGF agents must be assessed for overall risk of MA, and there is an unmet medical need to prevent the development of MA without undertreating wAMD.

摘要

年龄相关性黄斑变性(AMD)是导致失明的主要原因之一。晚期 AMD 可分为渗出性(通常称为湿性 AMD [wAMD])或干性 AMD,两者都可能进展为黄斑萎缩(MA)。MA 导致不可逆转的视力丧失,目前尚无批准的药物治疗方法。wAMD 的标准治疗方法是使用抗血管内皮生长因子(VEGF)治疗。然而,最近的证据表明,抗 VEGF 治疗可能在 MA 的发展中起作用。因此,重要的是要确定 wAMD 患者发生 MA 的风险因素。例如,通过频繁使用抗 VEGF 药物过度阻断 VEGF 可能会加速 MA 的发展。III 型黄斑新生血管(视网膜血管瘤样增生)的患者发生 MA 的风险特别高。这些患者的特征是存在预先存在的薄脉络膜(与年龄相关的脉络膜病变),表明脉络膜循环无法对增加的 VEGF 表达做出反应。有证据表明,视网膜下液(可能表明残留的 VEGF 活性)可能发挥保护作用。接受抗 VEGF 药物治疗的患者必须评估发生 MA 的总体风险,而且存在着未满足的医学需求,即在不过度治疗 wAMD 的情况下预防 MA 的发生。

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