Association of eNOS and ACE Polymorphisms with Retinopathy of Prematurity: A Systematic Review and Meta-Analysis

Fetal Pediatr Pathol. 2020 Aug;39(4):334-345. doi: 10.1080/15513815.2019.1652378. Epub 2019 Aug 22.

Abstract

Background: We performed a meta-analysis to clarify the association of endothelial nitric oxide synthase (eNOS) and angiotensin I-converting enzyme (ACE) gene polymorphisms with retinopathy of prematurity (ROP) risk. Methods: PubMed, Medline, and Embase literatures up to June 01, 2019, were reviewed. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the strength of associations. Results: Eighteen case-control studies including 14 studies (810 cases and 1754 controls) on eNOS polymorphisms and four studies (1014 cases and 1215 controls) on ACE I/D polymorphism were selected. Overall, analysis showed that infants with the ACE I/D polymorphism have an increased susceptibility to ROP. No association of eNOS 27-bp, 894 G > T and -786 T > C polymorphisms with ROP risk was found. Conclusion: ACE I/D polymorphism may serve as genetic biomarker of increased ROP risk. The eNOS polymorphisms do not appear to influence susceptibility to ROP.

Keywords: Retinopathy of Prematurity; angiotensin I-converting enzyme; endothelial nitric oxide synthase; meta-analysis; polymorphism.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Case-Control Studies
  • Genetic Predisposition to Disease
  • Humans
  • Infant, Newborn
  • Nitric Oxide Synthase Type III* / genetics
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic
  • Retinopathy of Prematurity* / genetics

Substances

  • NOS3 protein, human
  • Nitric Oxide Synthase Type III
  • ACE protein, human
  • Peptidyl-Dipeptidase A