Association between serum interleukln-1β levels and perinatal asphyxia

Objective:Asphyxia is a major cause of acute mortality and chronic neurologic disability in neonates. We sought to define the predictive values of serum concentrations of interleukin-1 p in newborns with perinatal asphyxia to see if there is a relation between interleukin-1 p (IL-ip) levels to the short term neurological deficit. Methods:This was a prospective (case-control) study conducted between June 2007 and July 2008, at the Neonatal Intensive Care Unit, Ghaem Hospital, Mashhad, Iran. Serum IL-ip levels were measured at birth, 24 and 48 h post-partum in 38 consecutive uninfected neonates with perinatal asphyxia(blood pH 7.2, lowApgar score, signs of fetal distress) and 41 randomly selected healthy newborns (normal infants free of a postnatal clinical event during the first weeks of life). Receiver-operating characteristic (ROC) curves were used for the determination of thresholds for the asphyxiated group versus healthy neonate group. Results:A total of 79 infants were studied. Serum interleukin-1 p concentrations in the infants who developed hypoxic-ischemic encephalopathy was 6 folds higher as compared to values in the normal infants (p 0.006) and 5-folds higher compared to infants with asphyxia who did not subsequently develop hypoxic-ischemic encephalopathy (p 0.006). There was also a significant relationship between serum IL-1B and outcome at the time of discharge. Conclusions:Serum levels of IL-1 B are increased substantially in neonates with asphyxia, and this is mostpronounced in neonates with poorer prognosis