A cross-sectional and diurnal study of thrombogenesis among patients with chronic atrial fibrillation

F L Li-Saw-Hee1, A D Blann, G Y Lip

  • 1University Department of Medicine, City Hospital, Birmingham, United Kingdom.

Insights

Patients with chronic atrial fibrillation (AF) exhibit a persistent hypercoagulable state without diurnal variation in key hemostatic factors. This sustained prothrombotic condition may increase stroke risk.

Area of Science:

  • Cardiology
  • Hematology
  • Thrombosis Research

Background:

  • Atrial fibrillation (AF) increases stroke and thromboembolism risk.
  • AF is linked to hypercoagulability, affecting thrombosis, platelet activation, and endothelial function.
  • Cardiovascular events like myocardial infarction involve thrombosis, which can show diurnal variation.

Purpose of the Study:

  • To investigate diurnal variation in hemostatic factors in chronic AF patients.
  • To compare levels of soluble thrombomodulin (sTM) and soluble P-selectin (sP-sel) in AF patients versus sinus rhythm controls.
  • To assess endothelial function and platelet activation markers in AF.

Main Methods:

  • Studied 52 chronic AF patients (no antithrombotic therapy) and matched controls.
  • Measured plasma fibrinogen, sP-sel, sTM, and von Willebrand factor (vWF) levels.
  • Collected serial blood samples from a subgroup over 24 hours to assess diurnal changes.

Main Results:

  • AF patients showed elevated plasma sP-sel, sTM, vWF, and fibrinogen compared to controls.
  • Significant correlations were observed between fibrinogen and sP-sel in both AF and control groups.
  • No significant diurnal variation was found for sP-sel, sTM, vWF, or fibrinogen in the 24-hour study.

Conclusions:

  • Chronic AF patients do not exhibit circadian or diurnal variation in their hypercoagulable state.
  • Persistent hypercoagulability and lack of diurnal variation in hemostatic markers in AF may elevate stroke and thromboembolic risk.
  • Findings highlight the continuous prothrombotic nature of chronic AF.
Abstract