Blue LED phototherapy in preterm infants: effects on an oxidative marker of DNA damagevan der Schoor, L. W. E., van Faassen, M. H. J. R., Kema, I., Baptist, D. H., Olthuis, A. J., Jonker, J. W., Verkade, H. J., Groen, H. & Hulzebos, C. V., 8-Apr-2020, In : ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION.
Research output: Contribution to journal › Article › Academic › peer-review
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 The use of fluorescent tube phototherapy is known to induce oxidative DNA damage in infants and has largely been replaced by blue light-emitting diode phototherapy (BLP).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: BLP did not alter urinary 8-OHdG/creatinine ratios (B=0.2, 95% CI -6.2 to 6.6) at either low (10-30 µW/cm2/nm) or high (>30 µW/cm2/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: BLP at irradiances up to 35 µW/cm2/nm given to preterm infants ≤32 weeks' gestation does not affect 8-OHdG, an oxidative marker of DNA damage.
|Journal||ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION|
|Publication status||E-pub ahead of print - 8-Apr-2020|