Altered fibrin clot properties and elevated von Willebrand factor are associated with progression to permanent atrial fibrillation: A cohort study
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Updated: Jun 1, 2025

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Karol Witold Nowak1,2, Michal Zabczyk1,3, Joanna Natorska1,3
1Department of Thromboembolic Disorders, Institute of Cardiology, Jagiellonian University Medical College, Krakow, Poland.
Insights
Altered blood clot properties, specifically longer clot lysis time and higher von Willebrand factor (vWF), predict atrial fibrillation (AF) progression to permanent AF (PerAF) even with anticoagulation.
Area of Science:
- Cardiology
- Hematology
- Thrombosis Research
Background:
- The prothrombotic state's role in atrial fibrillation (AF) progression to permanent AF (PerAF) is not fully understood.
- Denser, poorly lysable fibrin clots are observed in AF patients, correlating with increased stroke risk.
Purpose of the Study:
- To investigate if altered fibrin clot properties and prothrombotic markers predict the transition from AF to PerAF.
- To assess the association between baseline clot lysis time (CLT), von Willebrand factor (vWF), and other hemostatic markers with PerAF development.
Main Methods:
- A cohort study of 226 anticoagulated patients with paroxysmal or persistent AF.
- Baseline assessment of plasma clot permeability (Ks), CLT, fibrinolysis proteins, and vWF antigen.
- Follow-up for a median of 58 months to record PerAF development.
Main Results:
- PerAF developed in 27.4% of patients over 5.7%/year.
- Patients progressing to PerAF had significantly longer CLT, higher plasminogen activator inhibitor type 1, and higher vWF.
- Multivariable analysis identified CLT, vWF, and heart failure as independent predictors of PerAF progression.
Conclusions:
- Suppressed fibrin clot lysis and elevated vWF may drive AF progression to PerAF, even during anticoagulation.
- These findings suggest a link between blood coagulation abnormalities and AF progression.
Background:
The role of a prothrombotic state in atrial fibrillation (AF) progression to permanent arrythmia (PerAF) is unclear. Formation of denser and poorly lysable fibrin clots has been observed in AF patients also with sinus rhythm in association with higher stroke risk. We investigated whether altered fibrin clot properties and other prothrombotic state markers may contribute to AF transition to PerAF.
Methods:
In the cohort study, in 226 anticoagulated patients (median age 69 years, median CHA2DS2-VASc of 3) with paroxysmal (n = 83, 36.7%) or persistent (n = 143, 63.3%) AF, we assessed at baseline plasma clot permeability (Ks), clot lysis time (CLT), proteins involved in fibrinolysis and von Willebrand factor (vWF) antigen. We recorded patients with PerAF during a median follow-up of 58 months.
Results:
During follow-up, PerAF was documented in 62 (27.4%, 5.7%/year) subjects, who had higher prevalence of heart failure, higher body mass index and longer history of arrhythmia. AF transition to PerAF was associated with 25.7% longer CLT in relation to 21.3% higher plasminogen activator inhibitor type 1, and 29% higher vWF compared to the remainder, with no differences in Ks, plasminogen or α2-antiplasmin. By multivariable analysis, CLT (per 10 min, odds ratio [OR] 2.734, 95% confidence interval [CI] 1.788-4.180, p < .001), vWF (per 10%, OR 1.352, 95% CI 1.145-1.596, p < .001) and heart failure (OR 2.637, 95% CI 1.008-6.900, p = .048) were associated with progression to PerAF.
Conclusion:
Suppressed fibrin clot susceptibility to lysis and elevated vWF could contribute to progression to PerAF despite anticoagulation, which suggests links between blood coagulation and AF progression.
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