CHA2DS2VASc score and adverse outcomes in middle-aged individuals without atrial fibrillation

Author:

Renda Giulia1,Ricci Fabrizio234,Patti Giuseppe5,Aung Nay67,Petersen Steffen E67,Gallina Sabina12,Hamrefors Viktor38,Melander Olle38,Sutton Richard9,Engstrom Gunnar3,Caterina Raffaele De10,Fedorowski Artur311

Affiliation:

1. Institute of Cardiology, Department of Neuroscience, Imaging and Clinical Sciences, and Center of Excellence on Aging, CeSI-Met, G. d'Annunzio University, Chieti-Pescara, Italy

2. Institute of Advanced Biomedical Technologies, G. d'Annunzio University, Chieti-Pescara, Italy

3. Department of Clinical Sciences, Lund University, Malmö, Sweden

4. Fondazione Villa Serena per la Ricerca, Città Sant'Angelo (PE), Italy

5. Department of Cardiology, University of L'Aquila, Italy

6. William Harvey Research Institute, Queen Mary University of London, UK

7. Barts Heart Centre, St Bartholomew's Hospital, London, UK

8. Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden

9. National Heart and Lung Institute, Hammersmith Hospital Campus, London, UK

10. University Cardiology Division, Pisa University Hospital, Italy

11. Department of Cardiology, Skåne University Hospital, Malmö, Sweden

Abstract

Aims The CHA2DS2VASc score is used to evaluate the risk of thromboembolic events in patients with non-valvular atrial fibrillation. We assessed the prognostic yield of CHA2DS2VASc for new-onset atrial fibrillation, cardiovascular morbidity and mortality in a non-atrial fibrillation population. Methods We analysed a population-based cohort of 22,179 middle-aged individuals with ( n = 3542) and without ( n = 18,367) a history of atrial fibrillation; we grouped the population into five CHA2DS2VASc strata (0–1–2–3–≥4), and compared the risk of major adverse cerebro-cardiovascular events and mortality. Furthermore, we analysed the annual incidence of atrial fibrillation across different CHA2DS2VASc strata. Results Over a median follow-up of 15 years, 1572 patients (6.9%) had ischaemic strokes, 2162 (9.5%) coronary events and 5899 (26%) died. The cumulative incidence of ischaemic stroke in CHA2DS2VASc ≥ 4 subjects without atrial fibrillation was similar to patients with atrial fibrillation and CHA2DS2VASc 2, with a 10-year crude incidence rate of 0.91 (95% confidence interval (CI) 0.68–1.19) and 1.13 (95% CI 0.93–1.36) ischaemic strokes per 100 patient-years, respectively. CHA2DS2VASc in a non-atrial fibrillation population showed higher predictive accuracy for ischaemic stroke compared with an atrial fibrillation population (area under the curve 0.60 vs. 0.56; P = 0.001). In multivariable Cox regression analysis, CHA2DS2VASc ≥ 2 was an independent predictor of all-cause death (adjusted hazard ratio (aHR) 2.58; 95% CI 2.42–2.76), cardiovascular death (aHR 3.40; 95% CI 2.98–3.89), ischaemic stroke (aHR 2.20; 95% CI 1.92–2.53) and coronary events (aHR 1.83; 95% CI 1.63–2.04). The cumulative incidence of atrial fibrillation was greater with increasing CHA2DS2VASc strata, with an absolute annual incidence of more than 2% per year if CHA2DS2VASc ≥ 4. Conclusion The CHA2DS2VASc score is a sensitive tool for predicting new-onset atrial fibrillation and adverse outcomes in subjects both with and without atrial fibrillation.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

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