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Assessment of Plasma Coagulation on Liver Tissue in a Large Animal Model In Vivo
Published on: August 4, 2018
Importance of anticoagulant proteins in chronic liver diseases
Sebnem Gürsoy1, Mevlüt Başkol, Edip Torun
1Department of Gastroenterology, School of Medicine, Erciyes University, Kayseri, Turkey. sgursoy@erciyes.edu.tr
Insights
Antithrombin levels may indicate early liver damage in chronic active hepatitis. In cirrhosis, protein C, antithrombin, and D-dimer can assess disease severity and decompensation risk.
Area of Science:
- Hepatology
- Hematology
- Biochemistry
Background:
- Chronic liver disease, including cirrhosis and chronic active hepatitis, affects coagulation.
- Anticoagulant proteins play a crucial role in maintaining hemostasis.
- Understanding their levels can provide insights into disease progression.
Purpose of the Study:
- To investigate the significance of anticoagulant proteins in chronic liver disease.
- To explore their potential as biomarkers for disease severity.
- To correlate protein levels with liver function and damage.
Main Methods:
- Study included 35 cirrhosis patients, 15 chronic active hepatitis patients, and 10 healthy controls.
- Measured protein C, protein S, antithrombin, D-dimer, and thrombin time.
- Classified patients based on Child-Pugh score and disease activity.
Main Results:
- Cirrhotics showed decreased protein C, S, antithrombin, and increased D-dimer compared to controls.
- Protein C and antithrombin levels differed significantly in Child B and C patients.
- Chronic active hepatitis patients had low antithrombin levels, while other factors were normal.
Conclusions:
- Antithrombin may serve as an early marker for hepatocellular damage in chronic active hepatitis.
- Protein C and antithrombin are useful for assessing liver damage in cirrhotics.
- D-dimer levels may predict decompensation in cirrhosis.
Background/Aims:
This study was conducted to elucidate the importance of anticoagulant proteins in chronic liver disease and their possible role as markers in determining the severity of the liver disease.
Methods:
This study was conducted on 35 patients with cirrhosis, 15 patients with chronic active hepatitis and 10 healthy controls. Coagulation inhibitor proteins such as protein C, protein S and antithrombin, as well as D-dimer level and thrombin time, which reflect fibrin degradation products, were measured. Cirrhotic patients were categorized as Child A, B and C and chronic active hepatitis patients as mild or moderate activity according to the modified Knodell histopathologic classification. The parameters were compared between patient groups and healthy controls.
Results:
In comparison with controls, the cirrhotics had significantly decreased protein C, protein S, antithrombin levels and increased D-dimer levels. The Child B and Child C patients differed significantly with respect to protein C and antithrombin levels only. In the chronic active hepatitis patients, protein S, protein C and fibrinogen were within normal limits, whereas antithrombin was low.
Conclusions:
In chronic active hepatitis, the antithrombin level may be used as an early marker of hepatocellular damage. In cirrhotics, protein C and antithrombin may be useful for assessment of hepatocellular damage, whereas D-dimer may be important for the transition to decompensation.
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