Autor(es): Fevereiro-Martins, Mariza ; Santos, Ana Carolina ; Marques-Neves, Carlos ; Guimarães, Hercília ; Bicho, Manuel
Data: 2025
Identificador Persistente: http://hdl.handle.net/10400.5/98427
Origem: Repositório da Universidade de Lisboa
Assunto(s): Angiogenesis; Brain-derived neurotrophic factor; Erythropoietin; Gene expression; Nerve growth factor; Neurotrophic factors; Oxidative stress; Retinal vascular disease; Retinopathy of prematurity; Tyrosine hydroxylase
Retinal neurodevelopment, vascularization, homeostasis, and stress response are influenced by factors such as nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), tyrosine hydroxylase (TH), and erythropoietin (EPO). As retinopathy of prematurity (ROP) is a neurovascular retinal disease, this study analyzed the contributions of NGF (rs6330), BDNF (rs7934165), TH (rs10770141), and EPO (rs507392) genetic functional polymorphisms to the modulation of hematological and biochemical parameters of the first week of life and their association with ROP development. A multicenter cohort of 396 preterm infants (gestational age < 32 weeks or birth weight < 1500 g) was genotyped using MicroChip DNA and iPlex MassARRAY® platform. Multivariate regression followed univariate assessment of ROP risk factors. NGF (GG) genotype was associated with a higher ROP risk (OR = 1.79), which increased further (OR = 2.38) when epistatic interactions with TH (allele C) and BDNF (allele G) were present. Significant circulating biomarker differences, including bilirubin, erythrocytes, monocytes, neutrophils, lymphocytes, and platelet markers, were found between ROP and non-ROP groups, with variations depending on the polymorphism. These findings suggest that NGF (rs6330) and its interactions with related genes contribute to ROP risk, providing valuable insights into the genetic and biological mechanisms underlying the disease and identifying potential predictive biomarkers.
