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早产儿视网膜病变:分子发病机制的当前概念

Retinopathy of prematurity: current concepts in molecular pathogenesis.

作者信息

Heidary Gena, Vanderveen Deborah, Smith Lois E

机构信息

Department of Ophthalmology, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Semin Ophthalmol. 2009 Mar-Apr;24(2):77-81. doi: 10.1080/08820530902800314.

Abstract

Retinopathy of prematurity is marked by the proliferative vascularization of the retina in preterm babies. An understanding of the molecular pathogenesis of ROP provides the basis for identifying novel therapeutic targets for treatment. Using the mouse model of oxygen-induced retinopathy, the roles of the hypoxia induced factors vascular endothelial growth factor and erythropoietin as well as the maternally derived factors insulin-like growth factor-1 and omega-3 polyunsaturated fatty acids have begun to be elucidated. Understanding the phase specific effects of these factors will serve to guide the development of non destructive treatments for ROP and for other ischemic retinopathies including diabetic retinopathy and neovascular age-related macular degeneration.

摘要

早产儿视网膜病变的特征是早产婴儿视网膜出现增殖性血管化。对早产儿视网膜病变分子发病机制的理解为确定新的治疗靶点提供了基础。利用氧诱导性视网膜病变小鼠模型,缺氧诱导因子血管内皮生长因子和促红细胞生成素以及母体来源的因子胰岛素样生长因子-1和ω-3多不饱和脂肪酸的作用已开始得到阐明。了解这些因子的阶段特异性作用将有助于指导开发针对早产儿视网膜病变以及其他缺血性视网膜病变(包括糖尿病性视网膜病变和新生血管性年龄相关性黄斑变性)的非破坏性治疗方法。

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