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Clinical Trial
Is serum high-mobility group box 1 (HMGB-1) level correlated with liver fibrosis in chronic hepatitis B?
- Ahmet Cagkan Inkaya, Nazlim Aktug Demir, Servet Kolgelier, Sua Sumer, Lutfi Saltuk Demir, Onur Ural, Fatma Seher Pehlivan, Mahmure Aslan, and Abdullah Arpaci.
- Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Hacettepe University, Ankara Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Selçuk University, Konya Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Adiyaman University, Adiyaman Department of Public Health, Faculty of Medicine, Necmettin Erbakan University, Konya Department of Pathology, Adiyaman Education and Research Hospital, Adiyaman Department of Biochemistry, Adiyaman Education and Research Hospital, Adiyaman Department of Biochemistry, Faculty of Medicine, Adiyaman University, Adiyaman, Turkey.
- Medicine (Baltimore). 2017 Sep 1; 96 (36): e7547e7547.
BackgroundHigh-mobility group box 1 (HMGB1), identified as an alarmin molecule, was shown to have a role in virus-triggered liver injury. We aimed to evaluate the association between serum levels of HMGB1 and liver fibrosis.MethodThis cross-sectional case-control study included 189 chronic hepatitis B (CHB) patients and 51 healthy controls. All patients underwent liver biopsy and modified Knodell scoring system used to determine the fibrosis level in CHB patients. Serum HMGB1 levels were determined with enzyme-linked immunosorbent assay (ELISA).ResultsMean serum HMGB1 levels of patients (58.1 ± 54.7) were found to be higher than those of the control group (7.1 ± 4.3) (P = .001). HMGB1 levels of patients with advanced-stage fibrosis (stage 4 and 5) were detected to be higher than those of patients with early-stage fibrosis (stage 1-3). However, this difference was not statistically significant (P > .05). Albumin levels of fibrosis 3 and 4 patients were lower than fibrosis 1 and 2 patients. ALT, HBV DNA, and AFP levels of fibrosis 5 patients were significantly higher than fibrosis 1 and 2 patients, and their platelet and albumin levels are lower than fibrosis 1 and 2 patients (P < .001). In a logistic regression model, fibrosis levels were correlated with ALT values and inversely correlated with albumin levels.ConclusionIn this study, we demonstrated that serum HMGB1 levels increase in the early course of liver injury and this increase is not correlated with severity of the liver damage.
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