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Bilirubin-induced neural impairment: a special focus on myelination, age-related windows of susceptibility and associated co-morbidities.

Abstract
Bilirubin-induced neurologic dysfunction (BIND) and classical kernicterus are clinical manifestations of moderate to severe hyperbilirubinemia whenever bilirubin levels exceed the capacity of the brain defensive mechanisms in preventing its entrance and cytotoxicity. In such circumstances and depending on the associated co-morbidities, bilirubin accumulation may lead to short- or long-term neurodevelopmental disabilities, which may include deficits in auditory, cognitive, and motor processing. Neuronal cell death, astrocytic reactivity, and microglia activation are part of the bilirubin-induced pathogenesis. Less understood is how abnormal growth and maturation of oligodendrocytes may impact on brain development, affecting the formation of myelin tracts. Based on in-vitro and in-vivo models, as well as in clinical cases presented here, we propose the existence of impaired myelination by bilirubin with long-term sequelae, mainly in pre-term infants. Sensitive time-windows are highlighted and centered on the different developmental-dependent impairments determined by bilirubin, and the influence of sepsis and hypoxia is reviewed.
AuthorsDora Brites, Adelaide Fernandes
JournalSeminars in fetal & neonatal medicine (Semin Fetal Neonatal Med) Vol. 20 Issue 1 Pg. 14-19 (Feb 2015) ISSN: 1878-0946 [Electronic] Netherlands
PMID25534357 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2014 Elsevier Ltd. All rights reserved.
Chemical References
  • Bilirubin
Topics
  • Bilirubin (blood)
  • Comorbidity
  • Disease Susceptibility
  • Humans
  • Hyperbilirubinemia, Neonatal (blood, complications)
  • Hypoxia (complications)
  • Infant, Newborn
  • Infant, Premature
  • Kernicterus (blood, etiology)
  • Leukoencephalopathies (blood, etiology)
  • Nervous System Diseases (blood, etiology)
  • Sepsis (chemically induced)

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