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Blue LED phototherapy in preterm infants: effects on an oxidative marker of DNA damage

Lori W. E. van der Schoor, Martijn van Faassen, Ido P. Kema, Dyvonne H. Baptist, Annelies J Olthuis, Johan W. Jonker, Henkjan J. Verkade, Henk Groen, Christian V. Hulzebos

2020Archives of Disease in Childhood Fetal & Neonatal16 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Phototherapy is used on the majority of preterm infants with unconjugated hyperbilirubinaemia. The use of fluorescent tube phototherapy is known to induce oxidative DNA damage in infants and has largely been replaced by blue light-emitting diode phototherapy (BLP). To date, it is unknown whether BLP also induces oxidative DNA damage in preterm infants. OBJECTIVE: To determine whether BLP in preterm infants induces oxidative DNA damage as indicated by 8-hydroxy-2'deoxyguanosine (8-OHdG). DESIGN: Observational cohort study. METHODS: Urine samples (n=481) were collected in a cohort of 40 preterm infants (24-32 weeks' gestational age) during the first week after birth. Urine was analysed for the oxidative marker of DNA damage 8-OHdG and for creatinine, and the 8-OHdG/creatinine ratio was calculated. Durations of phototherapy and levels of irradiance were monitored as well as total serum bilirubin concentrations. RESULTS: /nm) irradiance: (B=2.3, 95% CI -5.7 to 10.2 and B=-3.0, 95% CI -11.7 to 5.6, respectively). Also, the 8-OHdG/creatinine ratios were independent on phototherapy duration (B=-0.1, 95% CI -0.3 to 0.1). CONCLUSIONS: /nm given to preterm infants ≤32 weeks' gestation does not affect 8-OHdG, an oxidative marker of DNA damage.

Topics & Concepts

Oxidative damageMedicineDNADNA damageOxidative phosphorylationOxidative stressGeneticsInternal medicineBiologyBiochemistryNeonatal Health and BiochemistryPhotodynamic Therapy Research StudiesRetinopathy of Prematurity Studies