Why the study?
The role of a prothrombotic state in atrial fibrillation progression to permanent arrhythmia remains unclear.
Do altered fibrin clot properties and elevated von Willebrand factor predict progression to permanent atrial fibrillation in anticoagulated patients with paroxysmal or persistent AF?
Do altered fibrin clot properties and elevated von Willebrand factor predict progression to permanent atrial fibrillation in anticoagulated patients with paroxysmal or persistent AF?
Suppressed fibrin clot susceptibility to lysis and elevated vWF are associated with progression to permanent atrial fibrillation in anticoagulated patients.
Answers are grounded in this paper and cite their sources.
May aid risk stratification for AF progression; hypothesis-generating and requires prospective validation before clinical use.
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 CHA 2 DS 2 ‐VASc of 3) with paroxysmal ( n = 83, 36.7%) or persistent ( n = 143, 63.3%) AF, we assessed at baseline plasma clot permeability (K s ), 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 K s , 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.
No takes yet. Share an insight, caveat, or question.
Nowak et al. (2025) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: