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Relationship Between Ventricular Arrhythmias, Conduction Disorders, and Myocardial Fibrosis in Patients With Systemic
Insights
Delayed-enhancement MRI detects myocardial fibrosis in most scleroderma patients. Fibrosis presence generally doesn't impact arrhythmias, but diffuse fibrosis is linked to more premature ventricular contractions (PVCs).
Area of Science:
- Cardiology
- Radiology
- Rheumatology
Background:
- Delayed-enhancement magnetic resonance imaging (DE-MRI) is a key tool for identifying myocardial fibrosis.
- The link between myocardial fibrosis and arrhythmias in scleroderma patients remains under-investigated.
Purpose of the Study:
- To explore correlations between ventricular arrhythmias, conduction disorders, and myocardial fibrosis in systemic sclerosis patients.
Main Methods:
- 36 scleroderma patients underwent ECG, 24-hour Holter monitoring, echocardiography, and cardiac DE-MRI.
- Gadolinium contrast was used in 33 of the DE-MRI scans.
Main Results:
- Myocardial fibrosis was found in 83.3% of patients via DE-MRI.
- 60% of patients exhibited ventricular arrhythmias or conduction disorders.
- No significant difference in arrhythmia burden or conduction disorders was observed between patients with and without fibrosis, except for a weak association between diffuse fibrosis and PVCs.
Conclusions:
- DE-MRI effectively identifies myocardial fibrosis in a majority of scleroderma patients.
- Myocardial fibrosis generally does not correlate with arrhythmia burden or conduction disorders.
- Diffuse fibrosis shows a modest association with an increased number of premature ventricular contractions per 24 hours.
Background:
Delayed-enhancement magnetic resonance imaging (DE-MRI) is a noninvasive diagnostic tool able to identify myocardial fibrosis. In patients with scleroderma, its relationship with arrhythmias and conduction disorders has not been fully explored.
Objectives:
The aim of this study was to evaluate the possible correlations between ventricular arrhythmias, conduction disorders, and myocardial fibrosis in patients with systemic sclerosis.
Methods:
Thirty-six patients with diffuse or limited cutaneous scleroderma underwent 12-lead electrocardiogram (ECG), 24-hour Holter ECG monitoring, transthoracic echocardiography, and cardiac DE-MRI, with gadolinium administration in 33 patients.
Results:
High-quality DE-MRI scans were obtained in 30 patients. Myocardial fibrosis was detected in 25 patients (83.3%). Eighteen patients (60%) had ventricular arrhythmias or conduction disorders. There was no significant difference in ventricular arrhythmia burden (the total number of premature ventricular contractions [PVCs]/24 hours) (48 ± 304 vs. 69 ± 236, P = 0.97), ventricular arrhythmia severity (couplets, triplets, runs) on Holter ECG, or in the presence of conduction disorders (36% vs. 40%, P = 0.86) between patients with and without myocardial fibrosis. In univariate analysis, diffuse fibrosis was weakly associated with the number of PVCs/24 hours (R = 0.157, P = 0.03). A number of at least 597 PVCs/24 hours had a sensitivity of 60% and a specificity of 92% in predicting the presence of diffuse fibrosis on DE-MRI (area under the curve = 0.640).
Conclusions:
Delayed-enhancement magnetic resonance imaging can identify myocardial fibrosis in a high percentage of scleroderma patients. Its presence does not seem to influence the ventricular arrhythmia burden and severity or the presence of conduction disorders, with the exception of diffuse myocardial fibrosis, which modestly influences the total number of PVCs/24 hours.
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