May oxidative stress biomarkers in cord blood predict the occurrence of necrotizing enterocolitis in preterm infants?

INTRODUCTION

Oxidative stress (OS) is strongly involved in the pathogenesis of many preterm newborn diseases; this is due to the low efficiency of neonatal antioxidant systems unable to counteract the harmful effects of free radicals (FRs). Hypoxic-ischemic events and inflammation, involved in necrotizing enterocolitis (NEC) pathogenesis, are responsible of the overproduction of FRs, generating OS.

AIM: To test the hypotesis that OS markers levels in cord blood may early identify the newborns at high risk to develop NEC.

MATERIALS AND

METHODS

332 preterm newborns of gestational age (GA) between 24 and 33 week and birth weight (BW) between 460 and 2540 g were consecutively recruited in three european neonatal intensive care units. Markers of potential OS risk: non-protein bound iron (NPBI), and markers of FRs damage: advanced oxidation protein products (AOPP) and total hydroperoxides (TH), were measured in the cord blood. Associations between NEC and OS markers were checked through inferential analysis.

RESULTS

Out of 332 preterm babies, 29 developed NEC. Babies with NEC had a BW and a GA significantly lower than healthy babies. AOPP, TH and NPBI cord blood levels were significantly higher in babies with NEC than in babies without (respectively mean AOPP = 28.05 ± 21 vs 15.80 ± 7.14; p < 0.05; TH = 154.48 ± 84.67 vs 107.40 ± 61.01; p < 0.05; NPBI = 2.21 ± 3.98 vs 0.95 ± 1.59; p < 0.05).

CONCLUSIONS

The determination of OS biomarkers in cord blood can be useful in identifying babies at high risk for NEC and in devising new strategies to ameliorate perinatal outcome.