Cerebral glucose utilisation in hepatitis C virus infection-associated encephalopathy

J Cereb Blood Flow Metab. 2011 Nov;31(11):2199-208. doi: 10.1038/jcbfm.2011.82. Epub 2011 Jun 1.

Abstract

Patients with hepatitis C virus (HCV) infection frequently show neuropsychiatric symptoms. This study aims to help clarify the neurochemical mechanisms behind these symptoms and to add further proof to the hypothesis that HCV may affect brain function. Therefore, 15 patients who reported increasing chronic fatigue, mood alterations, and/or cognitive decline since their HCV infection underwent neurologic and neuropsychological examination, magnetic resonance imaging, (18)F-fluoro-deoxy-glucose positron emission tomography of the brain, and single photon emission tomography of striatal dopamine and midbrain serotonin transporter (SERT) availability. None of the patients had liver cirrhosis. Patients' data were compared with data of age-matched controls. In addition, regression analysis was performed between cognitive deficits, and mood and fatigue scores as dependent variables, and cerebral glucose metabolism, dopamine, or SERT availability as predictors. Patients showed significant cognitive deficits, significantly decreased striatal dopamine and midbrain SERT availability, and significantly reduced glucose metabolism in the limbic association cortex, and in the frontal, parietal, and superior temporal cortices, all of which correlated with dopamine transporter availability and psychometric results. Thus, the study provides further evidence of central nervous system affection in HCV-afflicted patients with neuropsychiatric symptoms. Data indicate alteration of dopaminergic neurotransmission as a possible mechanism of cognitive decline.

MeSH terms

  • Brain / metabolism*
  • Brain Diseases, Metabolic / diagnostic imaging
  • Brain Diseases, Metabolic / etiology
  • Brain Diseases, Metabolic / metabolism*
  • Brain Diseases, Metabolic / psychology
  • Cognition / physiology
  • Dopamine / metabolism
  • Female
  • Fluorodeoxyglucose F18
  • Glucose / metabolism*
  • Hepatitis C / complications*
  • Hepatitis C / diagnostic imaging
  • Hepatitis C / metabolism
  • Humans
  • Luria-Nebraska Neuropsychological Battery
  • Memory / physiology
  • Positron-Emission Tomography
  • Radiopharmaceuticals
  • Serotonin Plasma Membrane Transport Proteins / metabolism
  • Tomography, Emission-Computed, Single-Photon

Substances

  • Radiopharmaceuticals
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins
  • Fluorodeoxyglucose F18
  • Glucose
  • Dopamine