Caspase-cleaved fragments of cytokeratin 18 in patients with chronic hepatitis B
| Autor: | Ramazan Kurt, Yusuf Yilmaz, Erol Avsar, Şükran Köse, Fatih Eren, Oya Yonal, Filiz Türe Özdemir, Osman Ozdogan |
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| Rok vydání: | 2010 |
| Předmět: |
Male
medicine.medical_specialty Clinical Biochemistry Biology Biochemistry Gastroenterology Cytokeratin Hepatitis B Chronic Internal medicine medicine Monoclonal Antibody M30 Humans Liver injury Keratin-18 Biochemistry (medical) Antibodies Monoclonal virus diseases General Medicine Middle Aged Hepatitis B medicine.disease Peptide Fragments digestive system diseases Liver ROC Curve HBeAg Apoptosis Case-Control Studies Caspases Immunology biology.protein Biomarker (medicine) Female Antibody Biomarkers |
| Zdroj: | Clinica Chimica Acta. 411:2029-2032 |
| ISSN: | 0009-8981 |
| Popis: | During hepatocyte apoptosis, intermediate filament protein cytokeratin 18 is cleaved by caspases at Asp396 which can be specifically detected by the monoclonal antibody M30 (M30-antigen). In this study, we sought to determine whether serum M30-antigen levels can serve as a useful biomarker of liver injury in the clinical spectrum of HBV infection.Serum M30-antigen levels were measured in inactive HBV carriers (n=54), patients with HBeAg-negative chronic hepatitis B (CHB, n=47), patients with HBeAg-positive CHB (n=42) and healthy controls (n=29). All subjects were treatment-naïve.There were significant differences in serum M30-antigen levels across the study groups (P0.001; Kruskal-Wallis test). Post hoc analyses revealed that M30-antigen levels did not differ significantly between inactive HBV carriers (median 109.6 U/L) and healthy controls (median 106.1 U/L). However, both patients with HBeAg-negative (CHB, median 182.9 U/L, P0.001) and HBeAg-positive CHB (median 158.3 U/L, P0.001) had significantly higher levels of M30-antigen compared with inactive HBV carriers.Hepatocyte apoptotic activity--as reflected by serum M30-antigen levels--is increased in chronic active hepatitis B, but is not associated with the HBeAg status. In contrast, apoptosis does not appear to be a prominent feature of inactive HBV carriers. |
| Databáze: | OpenAIRE |
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