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Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Predictors of atrial fibrillation in hypertrophic cardiomyopathy
Oliver P Guttmann1, Menelaos Pavlou2, Constantinos O'Mahony1
1University College London Institute for Cardiovascular Science and Barts Heart Centre, St. Bartholomew's Hospital, London, UK.
Insights
Identifying atrial fibrillation (AF) risk in hypertrophic cardiomyopathy (HCM) patients is possible using clinical factors. AF development in HCM patients indicates a poor prognosis, and antiarrhythmic drugs do not prevent it long-term.
Area of Science:
- Cardiology
- Internal Medicine
Background:
- Atrial fibrillation (AF) significantly increases morbidity and mortality in patients with hypertrophic cardiomyopathy (HCM).
- Predicting AF development in HCM patients is crucial for risk stratification and management.
Purpose of the Study:
- To identify predictors of AF in a large, multicenter HCM cohort.
- To investigate the association between AF and survival in HCM patients.
- To evaluate the efficacy of antiarrhythmic therapy in maintaining sinus rhythm (SR).
Main Methods:
- Retrospective, longitudinal cohort study of 4248 HCM patients (1986-2008).
- Multivariable Cox regression models used to identify AF predictors.
- Primary endpoint: AF detection via ECG, Holter, or device interrogation.
Main Results:
- 17.4% of HCM patients developed AF. Predictors included female sex, age, left atrial diameter, NYHA class, hypertension, and vascular disease.
- AF was associated with increased 10-year cardiovascular (10.9% vs. 4.9%) and non-cardiovascular (5.9% vs. 3.2%) mortality.
- Beta-blockers, calcium channel antagonists, and disopyramide temporarily maintained SR, while amiodarone did not prevent AF.
Conclusions:
- Readily available clinical parameters can identify HCM patients at risk for AF.
- AF development in HCM is linked to a poor prognosis.
- Current antiarrhythmic therapies do not offer long-term prevention of AF in HCM.
Objectives:
Atrial fibrillation (AF) is associated with increased morbidity and mortality in patients with hypertrophic cardiomyopathy (HCM). The primary aim of this study (HCM Risk-AF) was to determine the predictors of AF in a large multicentre cohort of patients with HCM. Exploratory analyses were performed to investigate the association between AF and survival and the efficacy of antiarrhythmic therapy in maintaining sinus rhythm (SR).
Methods:
A retrospective, longitudinal cohort of patients recruited between 1986 and 2008 in seven centres was used to develop multivariable Cox regression models fitted with preselected predictors. HCM was defined as unexplained hypertrophy (maximum left ventricular wall thickness of ≥15 mm or in accordance with published criteria for the diagnosis of familial disease). 28% of patients (n=1171) had coexistent hypertension. The primary end point was paroxysmal, permanent or persistent AF detected on ECG, Holter monitoring or implantable device interrogation.
Results:
Of the 4248 patients with HCM without pre-existing AF, 740 (17.4%) reached the primary end point. Multivariable Cox regression revealed an association between AF and female sex, age, left atrial diameter, New York Heart Association (NYHA) class, hypertension and vascular disease. The proportion of patients with cardiovascular death at 10 years was 4.9% in the SR group and 10.9% in the AF group (difference in proportions=5.9%; 95% CI (4.1% to 7.8%)). The proportion of patients with non-cardiovascular death at 10 years was 3.2% in the SR group and 5.9% in the AF group (difference in proportions=2.8%; 95% CI (0.1% to 4.2%)). An intention-to-treat propensity score analysis demonstrated that β-blockers, calcium channel antagonists and disopyramide initially maintained SR during follow-up, but their protective effect diminished with time. Amiodarone therapy did not prevent AF during follow-up.
Conclusion:
This study shows that patients with HCM who are at risk of AF development can be identified using readily available clinical parameters. The development of AF is associated with a poor prognosis but there was no evidence that antiarrhythmic therapy prevents AF in the long term.
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