ausblenden:
Schlagwörter:
VIRUS-INFECTION; CORE PROTEIN; ANTIBODIES; BIOMARKER; FACTOR-5; MICEComplement; Chronic hepatitis C; Inflammation; Fibrosis; Stellate cell;
Fibronectin;
Zusammenfassung:
Chronic hepatitis C viral infection modulates complement. The aim of this study was to determine whether complement analysis predicts liver inflammation and fibrosis in patients with chronic hepatitis C.
50 chronic hepatitis C patients who underwent a liver biopsy were compared to 50 healthy controls and 35 patients with various liver diseases. Total plasma complement activity (CH50) in plasma was diminished in hepatitis C patients suggesting complement activation. This decrease correlated with increased necrosis (r = -0.24, p < 0.05), and patients with levels below the normal range had a higher METAVIR activity score reflecting enhanced inflammation. SC5b-9, a marker of complement activation, correlated with inflammation (r = 0.40, p < 0.05), activity (r = 0.42, p < 0.05), and fibrosis scores (r = 0.49, p < 0.05). Finally, the prevalence of C1q auto-antibodies was higher in hepatitis C patients, and their presence was associated with increased inflammation and seemed to affect fibrosis.
We conclude that complement-induced liver inflammation contributes to fibrosis in patients with chronic hepatitis C. (C) 2013 Elsevier Inc. All rights reserved.
