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Type I plasminogen activator inhibitor 4G allele frequency is associated with chronic venous insufficiency
N Katrancioglu1, S Manduz, F Ozen
1Department of Cardiovascular Surgery, Heart Centre Building, Cumhuriyet University School of Medicine, Main Street, Sivas, Turkey. nurkay@gmail.com
Insights
Genetic variations in plasminogen activator inhibitor-1 (PAI-1) are linked to chronic venous insufficiency (CVI). The PAI-1 4G allele significantly increases the risk of developing CVI, impacting patient quality of life.
Area of Science:
- Vascular Medicine
- Genetics
- Coagulation Science
Background:
- Chronic venous insufficiency (CVI) is a prevalent condition affecting quality of life.
- Genetic factors, particularly coagulation abnormalities, may contribute to CVI pathogenesis.
- Plasminogen activator inhibitor-1 (PAI-1) regulates fibrinolysis, and its levels correlate with the PAI-1 4G/5G gene polymorphism.
Purpose of the Study:
- To investigate the association between the PAI-1 4G/5G gene polymorphism and chronic venous insufficiency.
- To determine if PAI-1 gene variants influence CVI risk.
Main Methods:
- Case-control study design.
- Genotyping of PAI-1 4G/5G polymorphism in 34 CVI patients and 34 age- and sex-matched controls.
- Statistical analysis to compare allele frequencies and assess risk.
Main Results:
- The PAI-1 4G allele was significantly more frequent in CVI patients (8.8% 4G/4G, 82.4% 4G/5G) compared to controls (2.9% 4G/4G, 41.2% 4G/5G).
- The PAI-1 4G allele was associated with a 3.25-fold increased risk of developing CVI.
- A clear relationship between CVI and the PAI-1 4G allele was observed.
Conclusions:
- The PAI-1 4G allele is a significant genetic risk factor for chronic venous insufficiency.
- This finding highlights the role of the fibrinolytic system in CVI pathogenesis.
- Further research into genetic predispositions for CVI is warranted.
Abstract:
Chronic venous insufficiency (CVI) is a common disease associated with poor quality of life. Genetic polymorphisms causing coagulation abnormalities may account for some of the CVI pathogenesis. Type I plasminogen activator inhibitor (PAI-1) is responsible for fibrinolytic system regulation, and plasma levels of PAI-1 are strongly correlated with PAI-1 4G/5G gene polymorphism. The association between PAI-1 4G/5G gene polymorphism and CVI was investigated. In 34 consecutive patients with clinically overt CVI, the PAI-1 4G/4G polymorphism was detected in three cases (8.8%); the 4G/5G polymorphism was detected in 28 (82.4%). In 34 age- and sex-matched controls, the PAI-1 4G/4G polymorphism was detected in one case (2.9%) and the 4G/5G polymorphism was detected in 14 cases (41.2%). The PAI-1 4G allele was found significantly more frequently in CVI patients than in controls. The 4G allele was associated with a 3.25-fold increase in CVI risk. Thus, a relationship between CVI and the PAI-1 4G allele is apparent.
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