The Limits of Biomarkers
Hepatitis C in Renal Disease, Hemodialysis and TransplantationThis flow develops the theme that laboratory measurements can reveal disease while also misleading clinicians in dialysis and transplantation.
increasing
Bearing strength in each event
decreasing
Quiet Enzymes

Quiet Enzymes
A misleading normality
Aminotransferase levels are often lower in dialysis patients, even when HCV viremia persists. Normal-range values may therefore conceal active liver injury.
Recalibrating interpretation
Clinicians must interpret laboratory data within renal context. A number loses meaning when the physiology that produced it has changed.
RNA Confirmation

RNA Confirmation
Infection versus memory
Anti-HCV antibodies show exposure but cannot distinguish resolved from active infection. HCV RNA testing establishes whether the virus remains present.
A decisive distinction
Treatment, transplant eligibility, and donor allocation depend on this difference. Molecular testing converts an ambiguous history into a current biological state.
Biopsy as Ground Truth

Biopsy as Ground Truth
Tissue over appearance
Liver biopsy stages fibrosis when enzymes and symptoms are unreliable. Kidney biopsy distinguishes HCV-related immune-complex injury from rejection and transplant glomerulopathy.
Invasive clarity
Biopsy carries bleeding, anxiety, and sampling limitations, yet it often provides the information on which major decisions depend. The theme is not that biomarkers are useless, but that they require anatomical confirmation.
during chronic Hemodialysis
after positive antibody testing
during pretransplant assessment or graft dysfunction