Prekallikrein behaviour in chronic active hepatitis and in cirrhotic patients

Haemostasis
|January 1, 1984
PubMed

Insights

In chronic active hepatitis and liver cirrhosis, prekallikrein (Prekk), antithrombin III (ATIII), and plasminogen levels are significantly decreased. Prekk may serve as a reliable indicator of protein liver failure.

Area of Science:

  • Hepatology
  • Clinical Biochemistry
  • Coagulation Science

Background:

  • Chronic active hepatitis and liver cirrhosis are associated with complex pathophysiological changes.
  • Coagulation factor levels can be altered in liver disease, impacting disease prognosis and management.

Purpose of the Study:

  • To evaluate prekallikrein (Prekk), antithrombin III (ATIII), plasminogen, and alpha 2-antiplasmin levels in patients with chronic active hepatitis and liver cirrhosis.
  • To correlate these protein levels with Normotest, a measure of overall blood coagulation function.
  • To determine if Prekk is a reliable index for protein liver failure.

Main Methods:

  • Quantitative measurement of Prekk, ATIII, plasminogen, and alpha 2-antiplasmin in patient serum.
  • Correlation analysis between protein levels and Normotest values.
  • Subgroup analysis of cirrhotic patients into compensated and decompensated states.

Main Results:

  • Prekk, ATIII, and plasminogen were significantly decreased in both chronic active hepatitis and liver cirrhosis groups compared to controls.
  • Alpha 2-antiplasmin levels were not significantly different in chronic active hepatitis but were significantly decreased in liver cirrhosis.
  • Prekk, ATIII, and plasminogen correlated significantly with Normotest in both disease groups. In decompensated cirrhosis, only Prekk showed a significant correlation with Normotest.

Conclusions:

  • Significant reductions in Prekk, ATIII, and plasminogen are characteristic of chronic active hepatitis and liver cirrhosis.
  • Alpha 2-antiplasmin is also reduced in liver cirrhosis, but not in chronic active hepatitis.
  • Prekallikrein (Prekk) emerges as a potential reliable biomarker for assessing protein liver failure, particularly in decompensated states.

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