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The genetics of retinopathy of prematurity: a model for neovascular retinal disease.

Authors :
Swan, Ryan
Swan, Ryan
Kim, Sang Jin
Campbell, J Peter
Paul Chan, RV
Sonmez, Kemal
Taylor, Kent D
Li, Xiaohui
Chen, Yii-Der Ida
Rotter, Jerome I
Simmons, Charles
Chiang, Michael F
Imaging and Informatics in ROP Research Consortium
Swan, Ryan
Swan, Ryan
Kim, Sang Jin
Campbell, J Peter
Paul Chan, RV
Sonmez, Kemal
Taylor, Kent D
Li, Xiaohui
Chen, Yii-Der Ida
Rotter, Jerome I
Simmons, Charles
Chiang, Michael F
Imaging and Informatics in ROP Research Consortium
Source :
Ophthalmology. Retina; vol 2, iss 9, 949-962; 2468-7219
Publication Year :
2018

Abstract

TopicRetinopathy of prematurity (ROP) is a proliferative retinal vascular disease in premature infants, and is a major cause of childhood blindness worldwide. In addition to known clinical risk factors such as low birth weight and gestational age, there is a growing body of evidence supporting a genetic basis for ROP.Clinical relevanceWhile comorbidities and environmental factors have been identified as contributing to ROP outcomes in premature infants, most notably gestational age and oxygen, some infants progress to severe disease despite absence of these clinical risk factors. The contribution of genetic factors may explain these differences and allow better detection and treatment of infants at risk for severe ROP.MethodsTo comprehensively review genetic factors that potentially contribute to the development and severity of ROP, we conducted a literature search focusing on the genetic basis for ROP. Terms related to other heritable retinal vascular diseases like "familial exudative vitreoretinopathy", as well as to genes implicated in animal models of ROP, were also used to capture research in diseases with similar pathogenesis to ROP in humans with known genetic components.ResultsContributions across several genetic domains are described including vascular endothelial growth factor, the Wnt signaling pathway, insulin-like growth factor 1, inflammatory mediators, and brain-derived neurotrophic factor.ConclusionsMost candidate gene studies of ROP have limitations such as inability to replicate results, conflicting results from various studies, small sample size, and differences in clinical characterization. Additional difficulty arises in separating the contribution of genetic factors like Wnt signaling to ROP and prematurity. Although studies have implicated involvement of multiple signaling pathways in ROP, the genetics of ROP have not been clearly elucidated. Next-generation sequencing and genome-wide association studies have potential to expand future underst

Details

Database :
OAIster
Journal :
Ophthalmology. Retina; vol 2, iss 9, 949-962; 2468-7219
Notes :
application/pdf, Ophthalmology. Retina vol 2, iss 9, 949-962 2468-7219
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391586211
Document Type :
Electronic Resource