Marburg I polymorphism of factor VII-activating protease is associated with idiopathic venous thromboembolism

Berthold Hoppe1, Farzaneh Tolou, Hartmut Radtke

  • 1Institutee of Transfusion Meidicine, Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. berthold.hoppe@charite.de

Blood
|October 16, 2004
PubMed

Insights

The factor VII-activating protease (FSAP) Marburg I variant is linked to an increased risk of venous thromboembolism (VTE). This finding suggests FSAP Marburg I may be an independent risk factor for VTE occurrence, especially in idiopathic cases.

Area of Science:

  • Vascular Biology
  • Hemostasis and Thrombosis
  • Genetic Risk Factors

Background:

  • The factor VII-activating protease (FSAP) Marburg I variant is known to affect the profibrinolytic system.
  • Previous research indicated FSAP Marburg I predicts carotid stenosis progression.

Purpose of the Study:

  • To investigate the association between the FSAP Marburg I variant and the risk of developing venous thromboembolism (VTE).

Main Methods:

  • A case-control study design was employed.
  • The frequency of the FSAP Marburg I variant was compared between patients with VTE and healthy controls.
  • Logistic regression analysis was used to determine independent risk factors.

Main Results:

  • FSAP Marburg I was significantly more frequent in patients with a history of VTE (8.0%) and idiopathic VTE (11.7%) compared to controls (2.3%).
  • Logistic regression confirmed FSAP Marburg I as an independent risk factor for VTE (OR, 3.5) and idiopathic VTE (OR, 6.2).

Conclusions:

  • The FSAP Marburg I variant is associated with an increased risk of venous thromboembolism.
  • FSAP Marburg I may serve as a significant independent risk factor for VTE, particularly for idiopathic VTE.

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