Effects of supplemental oxygen on urinary 8-hydroxy-2'-deoxyguanosine levels in extremely low birth weight infants

• Published in: Free radical research Vol. 48; no. 11; pp. 1285 - 1290
• Main Authors: Kato, E., Ibara, S., Kumazawa, K., Maruyama, Y., Tokuhisa, T., Matsui, T., Shimono, R., Maede, Y., Minakami, H.
• Format: Journal Article
• Language: English
• Published: England Informa Healthcare 01.11.2014; Taylor & Francis
• Subjects: biomarker; Birth Weight; Deoxyguanosine - analogs & derivatives; Deoxyguanosine - urine; Female; Gestational Age; Humans; Infant, Extremely Low Birth Weight - urine; Infant, Newborn; Infant, Premature; Obstetric Labor, Premature - urine; Oxidative Stress; Oxygen - administration & dosage; Oxygen - metabolism; oxygen supplementation; Pregnancy; preterm infants; reactive oxygen species; oxygen supplementation; biomarker; preterm infants; oxidative stress; reactive oxygen species
• DOI: 10.3109/10715762.2014.951841
• ISSN: 1071-5762

Abstract As the effects of supplementary oxygen on urinary excretion of 8-hydroxy-2'-deoxyguanosine (8-OHdG) are poorly understood, urinary 8-OHdG levels (ng/mg creatinine) were determined longitudinally on the postnatal day (PND) 1, 3, and 30 in 16 neonates with birth weight < 1000 g. No supplementary oxygen was required in 9 neonates during the first 24 h of life. Urinary 8-OHdG level on PND 1 was inversely correlated with birth weight in these 9 neonates (P = 0.0323) and was higher in four with birth weight < 750 g than five with birth weight > 750 g (41.0 ± 6.9 vs. 5.6 ± 2.7, respectively, P = 0.0200). Median urinary 8-OHdG on PND 1 of these 9 neonates was significantly lower than that of 7 neonates with oxygen (9.3 vs. 60.2, respectively), although there were no significant differences in clinical background, such as birth weight, between the two groups. Five of the 9 did not require supplemental oxygen at all during the first 30 days of life. Median urinary 8-OHdG levels were consistently significantly lower in the 5 neonates than in 11 neonates with oxygen transiently or persistently (9.3 vs. 54.6, 19.1 vs. 61.4, and 28.3 vs. 145 on PND 1, 3, and 30, respectively), although there were no differences in clinical background, such as birth weight, between the two groups. Urinary 8-OHdG on PND 30 was significantly positively correlated with supplemental oxygen dose on PND 30 (P < 0.0001), but not with birth weight in the 16 neonates. These results suggest that higher supplemental oxygen tension caused higher urinary 8-OHdG in this population.