Key result
HCV RNA-negative strands, indicating viral replication, were found in the subcortical white matter and cerebral cortex of two patients with recurrent hepatitis C and severe depression.
Why the study?
Is hepatitis C virus replication present in the brain tissue of patients with recurrent hepatitis C and severe depression?
Case Report (n=2)
Is hepatitis C virus replication present in the brain tissue of patients with recurrent hepatitis C and severe depression?
The detection of HCV replicative forms in brain tissue supports the concept of HCV neuroinvasion, potentially explaining neuropsychiatric symptoms like depression in chronic hepatitis C patients.
Supports HCV neuroinvasion in severe depression; leaves open whether brain replication drives neuropsychiatric symptoms in chronic hepatitis C.
Patients with chronic hepatitis C frequently report tiredness, easy fatigability, and depression. The aim of this study is to determine whether hepatitis C virus (HCV) replication could be found in brain tissue in patients with hepatitis C and depression. We report two patients with recurrent hepatitis C after liver transplantation who also developed severe depression. One patient died of multiorgan failure and the other, septicemia caused by Staphylococcus aureussis. Both patients had evidence of severe hepatitis C recurrence with features of cholestatic fibrosing hepatitis. We were able to study samples of their central nervous system obtained at autopsy for evidence of HCV replication. The presence of HCV RNA-negative strand, which is the viral replicative form, was determined by strand-specific Tth-based reverse-transcriptase polymerase chain reaction. Viral sequences were compared by means of single-strand conformation polymorphism and direct sequencing. HCV RNA-negative strands were found in subcortical white matter from one patient and cerebral cortex from the other patient. HCV RNA-negative strands amplified from brain tissue differed by several nucleotide substitutions from serum consensus sequences in the 5' untranslated region. These findings support the concept of HCV neuroinvasion, and we speculate that it may provide a biological substrate to neuropsychiatric disorders observed in patients with chronic hepatitis C. The exact lineage of cells permissive for HCV replication and the possible interaction between viral replication and cerebral function that may lead to depression remain to be elucidated.
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Vargas et al. (2002) conducted a case report in Recurrent hepatitis C after liver transplantation with severe depression (n=2). Hepatitis C virus (HCV) replication in brain tissue was evaluated on Presence of HCV RNA-negative strand in brain tissue. HCV RNA-negative strands, indicating viral replication, were found in the subcortical white matter and cerebral cortex of two patients with recurrent hepatitis C and severe depression.
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