IMR Press / FBE / Volume 1 / Issue 2 / DOI: 10.2741/E54

Frontiers in Bioscience-Elite (FBE) is published by IMR Press from Volume 13 Issue 2 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Open Access Article

Urinary S100A1B and S100BB to predict hypoxic ischemic encephalopathy at term

Show Less
1 Department of Neonatology, Cairo University, Cairo, Egypt
2 Perinatal Research Laboratory Department of Cardiac Surgery, S. Donato Milanese University Hospital, Milan, Italy
3 Department of Pediatrics and Neuroscience G. Gaslini Children’s University Hospital, Genoa, Italy
4 Institute of Anatomy and Cell Biology, Catholic University, I-00168 Rome, Italy
5 Department of Pediatrics, Obstetrics and Reproductive Medicine, University of Siena, Siena, Italy
6 Biochemical and Clinical Laboratory, San Martino Hospital, Genoa, Italy
7 Neonatal Intensive Care Unit, C. Arrigo Children’s Hospital, Alessandria, Italy
Academic Editor:Diego Gazzolo
Front. Biosci. (Elite Ed) 2009, 1(2), 560–567; https://doi.org/10.2741/E54
Published: 1 June 2009
(This article belongs to the Special Issue Clinical and biochemical markers and fetal-neonatal development)
Abstract

Urinary S100A1B and S100BB were measured to detect cases at risk of hypoxic-ischemic encephalopathy (HIE) in asphyxiated newborns. We recruited 42 asphyxiated infants and 63 healthy term neonates. S100A1B and S100BB were measured at first urination (time 0) and at 4 (time 1), 8 (time 2), 12 (time 3), 16 (time 4), 20 (time 5), 24 (time 6), 72 (time 7) hours after birth. 20 infants had no/mild HIE with good prognosis (Group A) and 22 had moderate/severe HIE with a greater risk of neurological handicap (Group B). Urine S100A1B and S100BB levels were significantly (P less than 0.0.01, for all) higher at all monitoring time-points in Group B than Group A and controls, but not between Group A and controls. Both S100A1B and S100BB have great sensitivity and specificity for HIE since their first measurement. In conclusion, S100A1B and S100BB are increased in urine collected from asphyxiated newborns who will develop HIE since first urination, and their measurement may be useful to early predict HIE when monitoring procedures are still of no avail.

Share
Back to top