早产儿视网膜病变血清代谢通路研究进展

发布时间：2018-04-02 17:14

本文选题：早产儿视网膜病变　切入点：血清　出处：《眼科新进展》2016年09期

【摘要】：早产儿视网膜病变(retinopathy of prematurity,ROP)是一类发生于早产、低体质量儿的视网膜血管异常增殖性致盲眼病。目前,ROP发病机理尚不清楚。深入研究ROP病理生理变化和发病机制,并采取有效措施阻断这一过程,将有利于从根本上预防ROP或阻止ROP严重病变的发生。寻找可用于ROP诊断的潜在血清特异性标志物,可为ROP发病机制研究和临床试验奠定基础。本文对ROP血清代谢通路研究新进展进行综述。
[Abstract]:Retinopathy of prematurity retinopathy (ROP) is a kind of retinal vascular dysproliferative blindness caused by premature birth and low body mass infants.At present, the pathogenesis of ROP is not clear.To study the pathophysiological changes and pathogenesis of ROP and to take effective measures to block this process will be beneficial to prevent ROP or prevent the occurrence of serious ROP lesions.To search for potential serum specific markers for the diagnosis of ROP can lay a foundation for the study of pathogenesis and clinical trials of ROP.This article reviews the recent advances in the study of serum metabolic pathways in ROP.
【作者单位】：贵州医科大学附属医院眼科;深圳市眼科医院;
【基金】：深圳市科创委基础研究项目(编号:JCY20140414114-853651、CXZZ201305161-6181591)~~
【分类号】：R774.1

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