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决定年龄相关性黄斑变性的因素:当前观点。

Factors determining age-related macular degeneration: a current view.

机构信息

Department of Ophthalmology, Kaunas University of Medicine, Eiveniu 2, 50009 Kaunas, Lithuania.

出版信息

Medicina (Kaunas). 2010;46(2):89-94.

Abstract

Age-related macular degeneration affects the macula and is the leading cause of significant and irreversible central visual loss. It is the most common cause of visual loss in people older than 60 years. The pathogenesis of age-related macular degeneration is complex and not completely understood. It is thought that age-related macular degeneration has a multifactorial etiology, the development of which may be caused by interrelation of environmental and genetic factors and body characteristics. In this article, risk factors such as age, gender, cigarette smoking, color of the iris, nutrition, body mass index, oxidative stress, and genetic factors (complement factor H gene, Apo E gene, and others) are reviewed. Here, choroidal neovascularization process, in which hypoxia, inflammatory process, and proteolytic enzymes play a determinant role, is discussed. Considerable attention is paid to genetic polymorphism of matrix metalloproteinases, especially to matrix metalloproteinases 2 and 9, respectively gelatinases A and B, also to matrix metalloproteinase 9.

摘要

年龄相关性黄斑变性影响黄斑,是导致严重且不可逆转的中心视力丧失的主要原因。它是 60 岁以上人群视力丧失的最常见原因。年龄相关性黄斑变性的发病机制复杂,尚未完全阐明。人们认为年龄相关性黄斑变性具有多因素病因,其发展可能是由环境和遗传因素以及身体特征的相互关系引起的。本文综述了年龄、性别、吸烟、虹膜颜色、营养、体重指数、氧化应激和遗传因素(补体因子 H 基因、载脂蛋白 E 基因等)等危险因素。这里讨论了脉络膜新生血管化过程,其中缺氧、炎症过程和蛋白水解酶起决定作用。人们对基质金属蛋白酶的遗传多态性给予了相当大的关注,特别是明胶酶 A 和 B,即基质金属蛋白酶 2 和 9,以及基质金属蛋白酶 9。

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