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Subclinical myocardial edema and arrhythmic burden in mitral valve prolapse: Insights from T2 mapping
Francesco Mangini1, Antonio Di Monaco1, Luca Sgarra1
1Department of Cardiology, Ospedale Regionale "Miulli", Acquaviva delle Fonti (BA), Italy.
Abstract:
Mitral valve prolapse is a common condition often considered benign; however, its association with arrhythmogenic risks is well-established, particularly when linked with mitral annular disjunction and myocardial fibrosis. Edema often precedes fibrosis in many clinical conditions, and both edema and myocardial fibrosis are detectable in vivo using cardiac magnetic resonance imaging. In cases of mild or chronic edema (subclinical edema), standard T2-weighted sequences may not be sufficient for identification; however, T2 mapping sequences can detect such edema. This study aimed to assess whether subclinical myocardial edema identified through T2 mapping is related to arrhythmic burden in patients with mitral valve prolapse and mitral annular disjunction, even in the absence of fibrosis. Thirty-four patients underwent cardiac magnetic resonance imaging and were classified into low and high arrhythmic burden groups based on the Lown grading system. Inclusion criteria were normal myocardial signal intensity on conventional T2-weighted imaging, non-hemodynamically significant mitral regurgitation, presence of mitral annular disjunction, and absence of fibrosis. The analysis was twofold: segmental, comparing native T2 times between corresponding myocardial segments of the groups; and regional, contrasting basal segments of the lateral, inferolateral, and inferior walls, typically more affected by mitral valve prolapse, with remote myocardium within each group. Patients with higher arrhythmic burdens showed elevated native T2 times, indicating subclinical myocardial edema in the basal myocardial segments. This suggests that even without fibrosis, early myocardial alterations related to mitral valve prolapse may be related to arrhythmic risks. The clinical implications are significant, advocating the integration of T2 mapping into routine evaluations to enhance therapeutic decision making and patient outcomes. The early detection of myocardial changes may allow timely intervention and potentially modify the disease course. Further research is needed to confirm these findings and explore the utility of T2 mapping in managing mitral valve prolapse, even in patients without mitral annular disjunction.
Insights
Subclinical myocardial edema, detected by T2 mapping in mitral valve prolapse patients with mitral annular disjunction, is linked to higher arrhythmic burden, even without fibrosis. Early detection may improve patient outcomes.
Area of Science:
- Cardiology
- Medical Imaging
- Cardiac Electrophysiology
Background:
- Mitral valve prolapse (MVP) is common, but its association with arrhythmias, especially with mitral annular disjunction (MAD) and fibrosis, is a concern.
- Subclinical myocardial edema, a precursor to fibrosis, can be detected using advanced cardiac magnetic resonance imaging (CMR) techniques like T2 mapping, which are more sensitive than standard T2-weighted sequences.
- Identifying early myocardial changes is crucial for understanding and managing arrhythmic risks in MVP patients.
Purpose of the Study:
- To investigate the relationship between subclinical myocardial edema, identified by T2 mapping, and arrhythmic burden in patients with MVP and MAD.
- To determine if T2 mapping can detect edema in the absence of fibrosis and its correlation with arrhythmias.
Main Methods:
- Cardiac magnetic resonance imaging (CMR) including T2 mapping was performed on 34 patients with MVP and MAD.
- Patients were categorized into low and high arrhythmic burden groups based on the Lown grading system.
- Analysis compared native T2 times (indicating edema) in basal myocardial segments between groups, excluding patients with significant regurgitation, fibrosis, or abnormal T2-weighted signals.
Main Results:
- Patients with a higher arrhythmic burden exhibited elevated native T2 times in basal myocardial segments, signifying subclinical myocardial edema.
- This finding persisted even in the absence of detectable myocardial fibrosis on CMR.
- The basal segments of the lateral, inferolateral, and inferior walls showed the most significant alterations.
Conclusions:
- Subclinical myocardial edema, detectable by T2 mapping, is associated with increased arrhythmic burden in MVP patients with MAD, independent of fibrosis.
- These early myocardial changes may represent a risk factor for arrhythmias.
- Integrating T2 mapping into routine CMR evaluations could enhance risk stratification and guide therapeutic decisions for MVP patients.
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