<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Choreziak-Michalak A</submitter><funding>Research Grant of Doctoral School, Poznan University of Medical Sciences</funding><pagination>78</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9960447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>The aim of this study was to investigate the association between selected polymorphisms of nitric oxide synthetase (eNOS) and endothelin-1 (EDN-1) with the occurrence and progression of retinopathy of prematurity (ROP). A prospective study was conducted on 90 preterm infants (44 female), comparing 39 cases with ROP and 51 controls without ROP. Patients who developed ROP were further divided into two subgroups-those with spontaneous regression of the disease and those with ROP requiring treatment. We found that preterm infants with TT genotype eNOS 894G > T had a 12.8-fold higher risk of developing ROP requiring treatment (p = 0.02). Our results showed that allele T of eNOS894G > T polymorphism was significantly more prevalent in ROP patients requiring treatment (p = 0.029). We also investi</pubmed_abstract><journal>BMC ophthalmology</journal><pubmed_title>Potential role of eNOS and EDN-1 gene polymorphisms in the development and progression of retinopathy of prematurity.</pubmed_title><pmcid>PMC9960447</pmcid><funding_grant_id>502-14-11121500-45047</funding_grant_id><pubmed_authors>Szpecht D</pubmed_authors><pubmed_authors>Chmielarz-Czarnocinska A</pubmed_authors><pubmed_authors>Seremak-Mrozikiewicz A</pubmed_authors><pubmed_authors>Gotz-Wieckowska A</pubmed_authors><pubmed_authors>Choreziak-Michalak A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Potential role of eNOS and EDN-1 gene polymorphisms in the development and progression of retinopathy of prematurity.</name><description>The aim of this study was to investigate the association between selected polymorphisms of nitric oxide synthetase (eNOS) and endothelin-1 (EDN-1) with the occurrence and progression of retinopathy of prematurity (ROP). A prospective study was conducted on 90 preterm infants (44 female), comparing 39 cases with ROP and 51 controls without ROP. Patients who developed ROP were further divided into two subgroups-those with spontaneous regression of the disease and those with ROP requiring treatment. We found that preterm infants with TT genotype eNOS 894G > T had a 12.8-fold higher risk of developing ROP requiring treatment (p = 0.02). Our results showed that allele T of eNOS894G > T polymorphism was significantly more prevalent in ROP patients requiring treatment (p = 0.029). We also investi</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-21T17:24:05.782Z</modification><creation>2024-12-04T12:37:05.934Z</creation></dates><accession>S-EPMC9960447</accession><cross_references><pubmed>36829141</pubmed><doi>10.1186/s12886-023-02810-x</doi></cross_references></HashMap>