Retinopathy of Prematurity-Targeting Hypoxic and Redox Signaling Pathways

被引:8
作者
Zhang, Liyu [1 ]
Buonfiglio, Francesco [1 ]
Fiess, Achim [1 ]
Pfeiffer, Norbert [1 ]
Gericke, Adrian [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Ophthalmol, Langenbeckstr 1, D-55131 Mainz, Germany
关键词
retinopathy of prematurity; pathophysiology; signaling pathways; novel; molecular targets; ENDOTHELIAL-GROWTH-FACTOR; PREVENTS RETINAL NEOVASCULARIZATION; OXYGEN-INDUCED RETINOPATHY; MOUSE MODEL; MULTICENTER TRIAL; NADPH OXIDASE; BIRTH-WEIGHT; NITRIC-OXIDE; SUPPLEMENTAL OXYGEN; TYPE-1; RETINOPATHY;
D O I
10.3390/antiox13020148
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Retinopathy of prematurity (ROP) is a proliferative vascular ailment affecting the retina. It is the main risk factor for visual impairment and blindness in infants and young children worldwide. If left undiagnosed and untreated, it can progress to retinal detachment and severe visual impairment. Geographical variations in ROP epidemiology have emerged over recent decades, attributable to differing levels of care provided to preterm infants across countries and regions. Our understanding of the causes of ROP, screening, diagnosis, treatment, and associated risk factors continues to advance. This review article aims to present the pathophysiological mechanisms of ROP, including its treatment. Specifically, it delves into the latest cutting-edge treatment approaches targeting hypoxia and redox signaling pathways for this condition.
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页数:24
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