Am J Perinatol 2008; 25(4): 211-218
DOI: 10.1055/s-2008-1064931
© Thieme Medical Publishers

Proinflammatory Cytokine-Receptor Interaction Model Improves the Predictability of Cerebral White Matter Injury in Preterm Infants

W. Thomas Bass1 , E. Stephen Buescher2 , Pamela S. Hair3 , Larry E. White4 , J. Camille Welch5 , Bonnie L. Burke6
  • 1Division of Neonatal Medicine, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia
  • 2Division of Pediatric Infectious Disease, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia
  • 3Center for Pediatric Research, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia
  • 4Division of Child and Adolescent Neurology and Developmental Medicine, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia
  • 5Epidemiology and Biostatistics, Department of Pediatrics, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia
  • 6Department of Clinical Outcomes, Research and Epidemiology, Eastern Virginia Medical School, Norfolk, Virginia
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Publication History

Publication Date:
11 March 2008 (online)

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ABSTRACT

Proinflammatory cytokines have been variably linked to development of cerebral white matter injury (WMI) in preterm infants. Because soluble receptors tightly control cytokine bioactivity, we modeled cytokine-receptor interaction as a predictor of WMI. Plasma from 100 preterm infants was assayed for cytokines (tumor necrosis factor alpha, interleukin (IL-1β, IL-6) and their soluble receptors (sTNF-RI), sTNF-RII, sIL-1RA, and sIL-6R). Cranial ultrasound (US) results were correlated with cytokine and receptor concentrations individually and with cytokine-receptor interaction models (PROC LOGISTIC; SAS Software). Receiver operating characteristic curves were constructed to determine the predictability of WMI. Fifty-two infants with normal US exams were compared with 21 infants with evidence of WMI. There was no association between individual cytokine or receptor concentrations and the development of WMI. However, modeling cytokines with their soluble receptors significantly improved the predictability of WMI. We concluded that consideration of cytokine-receptor interaction may be more important than individual cytokine concentrations alone in determining the role of inflammation in the pathogenesis of WMI in preterm infants.

REFERENCES

W. Thomas BassM.D. 

Division of Neonatal Medicine, Children's Hospital of The King's Daughters, Eastern Virginia Medical School

825 Fairfax Avenue, Norfolk, VA, 23507