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Published on: July 3, 2014
Natural coagulation inhibitor proteins in young patients with cerebral ischemia
L Oláh1, M Misz, J Kappelmayer
1Department of Neurology, University of Debrecen, Faculty of Medicine, Debrecen, Hungary.
Insights
Coagulation and fibrinolytic abnormalities are common in young patients with acute cerebral ischemia. While many improve over time, impaired fibrinolysis and clotting pathway issues persist in some, highlighting the acute phase
Area of Science:
- Biochemistry
- Hematology
- Neurology
Background:
- Cerebral ischemia involves complex hemostatic disturbances.
- Understanding coagulation and fibrinolysis in young patients is crucial.
Purpose of the Study:
- To investigate coagulation and fibrinolytic pathway abnormalities in young patients with cerebral ischemia.
- To assess the temporal changes in these abnormalities.
Main Methods:
- Studied 53 young patients with cerebral ischemia.
- Assessed antithrombin-III, protein C, protein S activities, and activated protein C (APC) ratios.
- Measured plasminogen activator inhibitor-1, lipoprotein (a), and alpha-2-antiplasmin levels.
Main Results:
- 26/53 patients showed initial abnormalities in coagulation factors or APC ratios.
- Most abnormalities normalized within three months.
- Persistent issues included decreased protein S activity and APC resistance.
- Impaired fibrinolysis was frequent, with elevated plasminogen activator inhibitor-1, lipoprotein (a), and alpha-2-antiplasmin.
Conclusions:
- Coagulation and fibrinolytic system abnormalities are prevalent during the acute phase of cerebral ischemia in young individuals.
- These findings may be influenced by the acute phase response and disease process.
- Long-term monitoring may be necessary for specific coagulation and fibrinolytic defects.
Abstract:
Disturbances of coagulation and fibrinolytic pathways were studied in 53 young patients with cerebral ischemia. Upon admission 26 of 53 patients had abnormality in at least one of the antithrombin-III, protein C, protein S activities or in activated protein C (APC) ratios. Three months after the first examination the majority of the previously detected abnormalities returned to normal values and the most frequent alterations were decrease in protein S activity (3 patients) and APC resistance (3 patients). Conditions resulting in impaired fibrinolysis were frequently detected upon admission. Elevation of plasminogen activator inhibitor-1, lipoprotein (a), and alpha-2-antiplasmin was present in 23, 10, and 4 cases, respectively. It is concluded that abnormalities of coagulation as well as of the fibrinolytic systems are prevalent in the acute phase of cerebral ischemia, however, the results may be significantly influenced by the disease process or the acute phase effect.
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