Factors Associated with Progression of Atrial Fibrillation and Impact on All-Cause Mortality in a Cohort of European Patients
- PMID: 36769416
- PMCID: PMC9917523
- DOI: 10.3390/jcm12030768
Factors Associated with Progression of Atrial Fibrillation and Impact on All-Cause Mortality in a Cohort of European Patients
Abstract
Background: Paroxysmal atrial fibrillation (AF) may often progress towards more sustained forms of the arrhythmia, but further research is needed on the factors associated with this clinical course.
Methods: We analyzed patients enrolled in a prospective cohort study of AF patients. Patients with paroxysmal AF at baseline or first-detected AF (with successful cardioversion) were included. According to rhythm status at 1 year, patients were stratified into: (i) No AF progression and (ii) AF progression. All-cause death was the primary outcome.
Results: A total of 2688 patients were included (median age 67 years, interquartile range 60-75, females 44.7%). At 1-year of follow-up, 2094 (77.9%) patients showed no AF progression, while 594 (22.1%) developed persistent or permanent AF. On multivariable logistic regression analysis, no physical activity (odds ratio [OR] 1.35, 95% CI 1.02-1.78), valvular heart disease (OR 1.63, 95% CI 1.23-2.15), left atrial diameter (OR 1.03, 95% CI 1.01-1.05), or left ventricular ejection fraction (OR 0.98, 95% CI 0.97-1.00) were independently associated with AF progression at 1 year. After the assessment at 1 year, the patients were followed for an extended follow-up of 371 days, and those with AF progression were independently associated with a higher risk for all-cause death (adjusted hazard ratio 1.77, 95% CI 1.09-2.89) compared to no-AF-progression patients.
Conclusions: In a contemporary cohort of AF patients, a substantial proportion of patients presenting with paroxysmal or first-detected AF showed progression of the AF pattern within 1 year, and clinical factors related to cardiac remodeling were associated with progression. AF progression was associated with an increased risk of all-cause mortality.
Keywords: atrial fibrillation; atrial fibrillation type; death; outcomes; progression; registry; remodeling.
Conflict of interest statement
G.B.: small speaker fee from Bayer, Boston, Boehringer Ingelheim, Brystol Myers Squibb, Janssen and Sanofi. L.F.: consultant or speaker for Bayer, BMS/Pfizer, Boehringer Ingelheim, Medtronic, Novartis, and XO. F.M.: advisor fees Boehringer-Ingelheim; research grants Ferrer; speaker fees Boehringer-Ingelheim, Astra-Zeneca, Pfizer, and Bayer; TP: consultant for Bayer and Pfizer (no fees). G.A.D.: small speaker fees from Boehringer-Ingelheim, Pfizer, Bayer, Sanofi, and Zentiva; G.Y.H.L.: consultant and speaker for Bayer/Janssen, BMS/Pfizer, Boehringer Ingelheim, Anthem, and Daiichi-Sankyo. (No fees were directly received personally.) All the disclosures occurred outside the submitted work. The other authors have no disclosures to declare.
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