Neurocognitive outcome in patients with hypertyrosinemia type I after long-term treatment with NTBC

J Inherit Metab Dis. 2012 Mar;35(2):263-8. doi: 10.1007/s10545-011-9394-5. Epub 2011 Nov 9.

Abstract

Objective: The implementation of NTBC into treatment of hypertyrosinemia type I (HT I) greatly improved survival by prevention of acute liver failure and hepatocellular carcinoma. However, there are first reports of cognitive impairment in patients with elevated plasma tyrosine concentrations.

Methods: We here assess the neurocognitive development using standardized psychometric test batteries with respect to cognition, motor abilities and speech in nine early-treated patients with HT I under long-term NTBC treatment.

Results: High plasma tyrosine concentrations were frequently documented resulting in elevated 12-month median plasma tyrosine concentrations in seven out of nine patients. Plasma NTBC concentrations were generally in the lower therapeutic range. Five out of seven patients (71%) above 3 years of age had a total IQ score below the average. In addition, five out of seven patients above 3 years showed an inhomogenous test profile with significant differences between the different testing scales. Motor abilities were subnormal in four out of seven patients(57%). Cerebral MRI revealed no abnormalities. Logopedic evaluation in children at school age documented dysfunction or retardation in language development in all but one of the tested patients (80%), however, all but one patients had a migration background.

Conclusions: A high number of patients performed below normal in the assessment of development, motor function and speech. We propose intellectual impairment as long-term complication in HT type I with elevated plasma tyrosine under NTBC treatment as observed in other hypertyrosinemias. These findings remain to be reproduced in greater patient numbers.

MeSH terms

  • Cerebrum / drug effects
  • Child
  • Child, Preschool
  • Cognition / drug effects*
  • Cognition Disorders / blood
  • Cognition Disorders / chemically induced
  • Cognition Disorders / etiology*
  • Cognition Disorders / metabolism
  • Cyclohexanones / adverse effects*
  • Cyclohexanones / therapeutic use*
  • Enzyme Inhibitors / adverse effects
  • Enzyme Inhibitors / therapeutic use
  • Female
  • Humans
  • Infant
  • Language Development
  • Long-Term Care / methods
  • Male
  • Motor Activity / drug effects
  • Nitrobenzoates / adverse effects*
  • Nitrobenzoates / therapeutic use*
  • Psychometrics / methods
  • Time
  • Treatment Outcome
  • Tyrosine / blood
  • Tyrosinemias / blood
  • Tyrosinemias / drug therapy*
  • Tyrosinemias / psychology*

Substances

  • Cyclohexanones
  • Enzyme Inhibitors
  • Nitrobenzoates
  • Tyrosine
  • nitisinone