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Technical Briefs |
1 Department of Pediatrics, Obstetrics and Reproductive Medicine, University of Siena, Siena, Italy
2 Department of Pediatrics, Giannina Gaslini Childrens University Hospital, Genoa, Italy
3 Department of Neonatology, Childrens Memorial Health Institute, Warsaw, Poland
aaddress correspondence to this author at: Department of Pediatrics, Obstetrics and Reproductive Medicine, University of Siena, Policlinico "Le Scotte", Viale Bracci, 53100 Siena, Italy; fax 39-0577-233-454, e-mail petraglia@unisi.it
| The first 300 words of the full text of this article appear below. |
Hypoxic ischemic encephalopathy (HIE) is an important cause of mortality and morbidity in full-term newborns, and neurologic handicaps develop in
2528% of these infants (1)(2). The postasphyxia period is crucial because brain damage may be at a subclinical stage or its symptoms may be hidden by the effects of sedation, and radiologic assessment may still be unrevealing (3)(4). Because activin A is a growth factor produced in the central nervous system (CNS) (5)(6), mainly after brain injury to modulate neuronal survival against toxicity (7)(8)(9)(10)(11)(12)(13)(14), in the present study we investigated whether its concentrations in cerebrospinal fluid (CSF) collected from asphyxiated full-term newborns were higher in those developing HIE and whether this measurement could be useful for the early detection of postasphyxia HIE.
We conducted a longitudinal cohort study, recruiting any infants consecutively admitted (April 1998 through June 2002) to our Neonatal Intensive Care Units (NICUs), who underwent a lumbar puncture in the first 24-h from birth for clinical indications. We expected approximately one third of asphyxiated infants to exhibit moderate/severe HIE; we therefore planned to enroll 30 infants in the asphyxiated group (full-term infants with a gestational age >36 weeks), with at least 8 of them in the HIE subgroup, which would assure a statistical power of 90% to detect differences
10% between group means with a significance level of 95%. Considering that <40% of the infants submitted to lumbar puncture in our NICUs have a history of perinatal asphyxia, we expected that
4050 nonasphyxiated infants could be enrolled to the control group contemporarily with the 30 infants of the asphyxiated group. The Local Ethics Committees approved the study protocol, and parents
The following articles in journals at HighWire Press have cited this article:
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P. Florio, R. Felipe Abella, T. de la Torre, A. Giamberti, S. Luisi, G. Butera, A. Cazzaniga, A. Frigiola, F. Petraglia, and D. Gazzolo Perioperative Activin A Concentrations as a Predictive Marker of Neurologic Abnormalities in Children after Open Heart Surgery Clin. Chem., May 1, 2007; 53(5): 982 - 985. [Abstract] [Full Text] [PDF] |
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P. Florio, S. Luisi, B. Moataza, M. Torricelli, I. Iman, M. Hala, A. Hanna, F. Petraglia, and D. Gazzolo High Urinary Concentrations of Activin A in Asphyxiated Full-Term Newborns with Moderate or Severe Hypoxic Ischemic Encephalopathy Clin. Chem., March 1, 2007; 53(3): 520 - 522. [Abstract] [Full Text] [PDF] |
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P. Florio, S. Perrone, S. Luisi, P. Vezzosi, M. Longini, B. Marzocchi, F. Petraglia, and G. Buonocore Increased Plasma Concentrations of Activin A Predict Intraventricular Hemorrhage in Preterm Newborns Clin. Chem., August 1, 2006; 52(8): 1516 - 1521. [Abstract] [Full Text] [PDF] |
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