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Updated: May 17, 2026

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Diffuse ventricular fibrosis in atrial fibrillation: noninvasive evaluation and relationships with aging and systolic
Liang-Han Ling1, Peter M Kistler, Andris H Ellims
1Alfred Hospital and Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Insights
This study shows that contrast-enhanced T1 mapping can detect diffuse left ventricular (LV) fibrosis in patients with atrial fibrillation (AF). This technique offers new insights into how AF relates to adverse ventricular remodeling.
Area of Science:
- Cardiology
- Medical Imaging
- Biomedical Engineering
Background:
- Diffuse myocardial fibrosis is a key indicator of cardiomyopathy, often undetectable by standard cardiac magnetic resonance (CMR) imaging.
- Contrast-enhanced T1 mapping offers a method to quantify diffuse fibrosis, distinct from replacement fibrosis.
- In atrial fibrillation (AF), fibrosis may stem from the arrhythmia itself or indicate underlying cardiomyopathy.
Purpose of the Study:
- To assess diffuse left ventricular (LV) myocardial fibrosis in patients diagnosed with atrial fibrillation (AF).
Main Methods:
- Ninety participants (23 controls, 40 paroxysmal AF, 27 persistent AF) underwent CMR on a 1.5-T scanner.
- Cardiac morphology and function were assessed using cine imaging.
- Post-contrast T1 relaxation time (T1 time) of the LV myocardium was calculated using a validated T1 mapping sequence as a measure of diffuse myocardial fibrosis.
Main Results:
- Persistent AF patients exhibited larger left atrium volumes and reduced ejection fraction compared to controls and paroxysmal AF patients.
- Significant differences in post-contrast ventricular T1 time were observed across all groups (controls, paroxysmal AF, persistent AF).
- Age, AF category, and ejection fraction were identified as independent predictors of post-contrast T1 time after multivariate analysis.
Conclusions:
- Post-contrast T1 mapping is effective in identifying diffuse LV fibrosis in patients with AF.
- This imaging technique provides novel understanding of the relationship between AF and adverse ventricular remodeling.
Objectives:
The purpose of this study was to evaluate diffuse myocardial fibrosis of the left ventricle (LV) in patients with atrial fibrillation (AF).
Background:
Diffuse myocardial fibrosis is a hallmark of cardiomyopathy. Unlike replacement fibrosis, it is not visualized on delayed-enhancement cardiac magnetic resonance (CMR) imaging, but may be quantified with contrast-enhanced T(1) mapping methods. In atrial fibrillation (AF), it may be induced by arrhythmia or reflect pre-existing cardiomyopathy.
Methods:
Ninety subjects underwent CMR using a clinical 1.5-T scanner: 23 controls, 40 paroxysmal AF patients, and 27 persistent AF patients. Cardiac morphology and function was evaluated from CMR cine imaging. A histologically validated T(1) mapping sequence was used to calculate post-contrast T(1) relaxation time (T(1) time) of the LV myocardium as an index of diffuse myocardial fibrosis.
Results:
Age was similar across controls, paroxysmal AF patients, and persistent AF patients (54 ± 12 years, 58 ± 9 years, and 56 ± 10 years, p = NS). Persistent AF patients had larger indexed left atrium volume (55 ± 18 ml vs. 41 ± 12 ml and 47 ± 14 ml) and lower ejection fraction (54 ± 10% vs. 65 ± 6% and 61 ± 8%) than controls and paroxysmal AF patients (p < 0.05). Post-contrast ventricular T(1) time differed across all groups (controls, 535 ± 86 ms; paroxysmal AF, 427 ± 95 ms; persistent AF, 360 ± 84 ms; p < 0.001). Univariate predictors of post-contrast ventricular T(1) time included age, sex, AF category, ejection fraction, LV mass, congestive heart failure, and body mass index. After multivariate analysis, age, AF category, and ejection fraction remained independent predictors.
Conclusions:
Post-contrast ventricular T(1) mapping identifies diffuse LV fibrosis in patients with AF and provides new insights into the association between AF and adverse ventricular remodeling.
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