Complement Inhibitors for Geographic Atrophy in Age-Related Macular Degeneration-A Systematic Review.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Journal of Personalized Medicine Pub Date : 2024-09-17 DOI:10.3390/jpm14090990
Ana Maria Dascalu, Catalin Cicerone Grigorescu, Dragos Serban, Corneliu Tudor, Cristina Alexandrescu, Daniela Stana, Sanda Jurja, Andreea Cristina Costea, Catalin Alius, Laura Carina Tribus, Dan Dumitrescu, Dan Bratu, Bogdan Mihai Cristea
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Abstract

Background/objectives: Age-related macular degeneration (AMD) is one of the main causes of blindness and visual impairment worldwide. Intravitreal complement inhibitors are an emergent approach in the treatment of AMD, which have had encouraging results. This systematic review analyzes the outcomes and safety of complement inhibitor therapies for GA in AMD cases.

Methods: A comprehensive search on the PubMed and Web of Science databases returned 18 studies involving various complement inhibitor agents, with a total of 4272 patients and a mean follow-up of 68.2 ± 20.4 weeks.

Results: Most treated patients were white (96.8%) and female (55.8%), with a mean age of 78.3 ± 7.8 years and a mean GA area of 8.0 ± 3.9 mm2. There were no differences in visual function change between treated and control participants. The mean GA area change was 2.4 ± 0.7 mm2 in treated participants vs. 2.7 ± 0.8 mm2 in control groups (p < 0.001). The ocular and systemic side effects were similar to those of intravitreal anti-VEGF. A less-understood effect was that of the onset of choroidal neovascularization (CNV) in 1.1-13% of patients; this effect was found to be more frequent in patients with neovascular AMD in the fellow eye or nonexudative CNV in the study eye at baseline.

Conclusions: Complement inhibitors may represent a useful therapy for GA in AMD, but a personalized approach to patient selection is necessary to optimize the outcomes.

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补体抑制剂治疗老年性黄斑变性的地理萎缩--系统综述。
背景/目的:老年性黄斑变性(AMD)是导致全球失明和视力损伤的主要原因之一。玻璃体内补体抑制剂是治疗 AMD 的一种新兴方法,取得了令人鼓舞的效果。这篇系统性综述分析了补体抑制剂治疗AMD病例中GA的疗效和安全性:方法:在 PubMed 和 Web of Science 数据库中进行了全面检索,共检索到 18 项涉及各种补体抑制剂的研究,患者总人数为 4272 人,平均随访时间为 68.2 ± 20.4 周:大多数接受治疗的患者为白人(96.8%)和女性(55.8%),平均年龄为(78.3±7.8)岁,平均GA面积为(8.0±3.9)平方毫米。治疗组和对照组患者的视功能变化没有差异。治疗组的平均GA面积变化为2.4 ± 0.7 mm2,对照组为2.7 ± 0.8 mm2(P < 0.001)。眼部和全身副作用与玻璃体内抗 VEGF 相似。有1.1%-13%的患者会出现脉络膜新生血管(CNV),这是一种不太容易理解的副作用;研究发现,这种副作用在同侧眼有新生血管性AMD或基线时研究眼无渗出性CNV的患者中更为常见:补体抑制剂可能是治疗老年性视网膜病变的一种有效疗法,但要想取得最佳疗效,就必须对患者进行个性化选择。
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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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