A novel approach to study oxidative stress in neonatal respiratory distress syndrome

• Oxidative stress is important in the pathogenesis of neonatal respiratory distress syndrome (RDS).
• Oxidative stress biomarkers were studied in neonates with RDS.
• The high concentration of products of lipid peroxidation, protein damage and oxidative DNA damage were found.
• High oxidative stress was correlated with presence of RDS in newborns.
• Our results are an important step in continuous monitoring of the neonatal RDS.

BackgroundRespiratory distress syndrome of the neonate (neonatal RDS) is still an important problem in treatment of preterm infants. It is accompanied by inflammatory processes with free radical generation and oxidative stress. The aim of study was to determine the role of oxidative stress in the development of neonatal RDS.MethodsMarkers of oxidative stress and antioxidant activity in umbilical cord blood were studied in infants with neonatal respiratory distress syndrome with reference to healthy newborns.ResultsStatus of markers of oxidative stress (malondialdehyde, protein carbonyl and 8-hydroxy-2-deoxy guanosine) showed a significant increase with depleted levels of total antioxidant capacity in neonatal RDS when compared to healthy newborns.ConclusionThe study provides convincing evidence of oxidative damage and diminished antioxidant defenses in newborns with RDS. Neonatal RDS is characterized by damage of lipid, protein and DNA, which indicates the augmentation of oxidative stress.General significanceThe identification of the potential biomarker of oxidative stress consists of a promising strategy to study the pathophysiology of neonatal RDS.