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.

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