Circulating microparticles in patients with chronic hepatitis C and changes during direct-acting antiviral therapy
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
33928944
DOI
10.5507/bp.2021.023
Knihovny.cz E-resources
- Keywords
- chronic hepatitis C, direct-acting antivirotics, microparticles, microvesicles,
- MeSH
- Antiviral Agents therapeutic use MeSH
- Hepatitis C, Chronic * drug therapy MeSH
- Fibrosis MeSH
- Liver Cirrhosis drug therapy MeSH
- Humans MeSH
- Cell-Derived Microparticles * MeSH
- Sustained Virologic Response MeSH
- Inflammation MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antiviral Agents MeSH
BACKGROUND: Microparticles (MPs) are heterogeneous vesicles derived from membranes of different cells. Between 70 to 90% of MPs detected in blood originate from platelets. The release of MPs is associated with proinflammatory and procoagulant states. Elevated levels of MPs have been found in different diseases. We investigated MPs levels in patients with chronic hepatitis C (CHC) and changes in level during treatment using direct-acting antivirotics (DAA). PATIENTS AND METHODS: Thirty-six patients with CHC and forty healthy volunteers were included in the study. Concentrations of MPs were determined indirectly by measuring their procoagulant activity in plasma at baseline, end of therapy (EOT), and 12 weeks after EOT when the sustained virological response was assessed (SVR12). RESULTS: All patients achieved SVR12, which was associated with rapid improvement of markers of liver damage and function as well as liver stiffness (P=0.002). MPs levels were significantly higher in CHC patients than in healthy volunteers (P<0.001). No statistically significant decrease was found observed between baseline and SVR12 (P=0,330). Analysis of subpopulations with minimal fibrosis F0-1 (P=0.647), advanced fibrosis F2-4 (P=0.370), women(P=0.847), men (P=0.164) and genotype 1 (P=0.077) showed no significant changes during the follow-up period. CONCLUSIONS: MPs levels are higher in CHC patients and remain elevated shortly after achieving SVR. Higher concentrations of MPs in plasma are probably caused by a chronic uncontrolled exaggerated inflammatory response caused by CHC. Longer observation would probably confirm the significance of MPs levels decrease because normalization of liver function, inflammation, and structure after SVR requires more than 12 weeks.
Department of Hematology University Hospital Brno Jihlavska 20 62500 Brno Czech Republic
Department of Infectious Diseases University Hospital Brno Jihlavska 20 62500 Brno Czech Republic
Faculty of Medicine Masaryk University Kamenice 5 62500 Brno Czech Republic
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