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Published on: June 14, 2016
Diffuse myocardial fibrosis in patients with mitral valve prolapse and ventricular arrhythmia
An H Bui1,2, Sébastien Roujol2, Murilo Foppa2,3
1Cardiovascular Division, Department of Medicine, Harvard-Thorndike Electrophysiology Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Mitral valve prolapse (MVP) may indicate diffuse left ventricular (LV) myocardial fibrosis, detected by cardiac magnetic resonance (CMR) T1 imaging. This fibrosis is linked to arrhythmias, even without visible scarring.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Medical Research
Background:
- Mitral valve prolapse (MVP) is a common condition.
- The relationship between myocardial fibrosis and complex ventricular arrhythmias (ComVA) in MVP is not fully understood.
- Cardiac magnetic resonance (CMR) T1 imaging offers a method to assess diffuse myocardial fibrosis.
Purpose of the Study:
- To investigate the association between diffuse myocardial fibrosis, assessed by CMR T1, and ComVA in patients with MVP.
- To compare T1 times in MVP patients with and without ComVA, and with healthy controls.
Main Methods:
- Retrospective analysis of 41 MVP patients and 31 controls undergoing CMR.
- Measurement of left ventricular (LV) septal T1 times post-contrast administration.
- Arrhythmia analysis using Holter/event monitors in 23 MVP patients.
- Assessment of Late Gadolinium Enhancement (LGE) for focal fibrosis.
Main Results:
- MVP patients had significantly shorter postcontrast T1 times than controls (334±52 vs 363±58 ms; p=0.03).
- Patients with MVP and ComVA had shorter T1 times compared to those without ComVA (324 vs 354 ms; p=0.03).
- Only 36% of MVP patients with ComVA showed evidence of papillary muscle LGE, suggesting diffuse fibrosis.
Conclusions:
- Reduced postcontrast T1 times suggest diffuse LV myocardial fibrosis in MVP.
- This diffuse interstitial derangement may contribute to ComVA in MVP, even without focal fibrosis.
- CMR T1 imaging is a valuable tool for assessing myocardial fibrosis in MVP and its association with arrhythmias.
Objective:
We aimed to investigate the association of diffuse myocardial fibrosis by cardiac magnetic resonance (CMR) T1 with complex ventricular arrhythmia (ComVA) in mitral valve prolapse (MVP).
Methods:
A retrospective analysis was performed on 41 consecutive patients with MVP referred for CMR between 2006 and 2011, and 31 healthy controls. Arrhythmia analysis was available in 23 patients with MVP with Holter/event monitors. Left ventricular (LV) septal T1 times were derived from Look-Locker sequences after administration of 0.2 mmol/kg gadopentetate dimeglumine. Late gadolinium enhancement (LGE) CMR images were available for all subjects.
Results:
Patients with MVP had significantly shorter postcontrast T1 times when compared with controls (334±52 vs 363±58 ms; p=0.03) despite similar LV ejection fraction (LVEF) (63±7 vs 60±6%, p=0.10). In a multivariable analysis, LV end-diastolic volume, LVEF and mitral regurgitation fraction were all correlates of T1 times, with LVEF and LV end-diastolic volume being the strongest (p=0.005, p=0.008 and p=0.045, respectively; model adjusted R2=0.30). Patients with MVP with ComVA had significantly shorter postcontrast T1 times when compared with patients with MVP without ComVA (324 (296, 348) vs 354 (327, 376) ms; p=0.03) and only 5/14 (36%) had evidence of papillary muscle LGE.
Conclusions:
MVP may be associated with diffuse LV myocardial fibrosis as suggested by reduced postcontrast T1 times. Diffuse interstitial derangement is linked to subclinical systolic dysfunction, and may contribute to ComVA in MVP-related mitral regurgitation, even in the absence of focal fibrosis.
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