Bilirubin encephalopathy is neurological damage that is caused by high levels of unconjugated bilirubin.
Unconjugated bilirubin anion is unbound to albumin, enabling it to cross the blood-brain barrier, enter neurons, and disrupt energy metabolism, ultimately causing death.
Definition of terms
Term
Definition
Acute bilirubin encephalopathy
An early, potentially reversible neurotoxic effect of unconjugated bilirubin on the brain. It sets in at TSB > 20 – 25 mg/dL (340 – 425 umol/L)
Chronic bilirubin encephalopathy (Kernicterus)
Permanent brain damage due to bilirubin deposition in the basal ganglia. It sets in at > 30 mg/dL (> 510 umol/L). It is diagnosed by MRI. A post-mortem biopsy may show yellow staining of the basal ganglia (”Kern” = nuclei; “Icterus” = jaundice)
Immature liver UDP-glucuronosyltransferase activity and increased permeability of the BBB
Respiratory distress
Hypoxia-induced acidosis displaces bilirubin from albumin, and poor liver perfusion reduces bilirubin metabolism and clearance
Hypoxia
Decreased ATP production causes liver dysfunction and impaired bilirubin conjugation for clearance
Acidosis
Protons compete with bilirubin for albumin binding sites
Sepsis
Inflammatory cytokines increase the permeability of the BBB, endotoxins interfere with bilirubin conjugation, and hemolysis due to infection increases bilirubin load
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