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Published on: August 8, 2022
Rupture of mitral valve chordae in hypertrophic cardiomyopathy
Florence Boissier1, Guy Achkouty1, Patrick Bruneval2
1Department of Cardiology, hôpital Européen Georges Pompidou, Assistance publique-Hôpitaux de Paris, 75015 Paris, France.
Insights
Mitral valve chordal rupture is infrequent in hypertrophic cardiomyopathy, typically affecting older patients with obstructive disease. This condition often leads to severe mitral regurgitation requiring surgical intervention.
Area of Science:
- Cardiology
- Cardiac Surgery
- Pathology
Background:
- Mitral valve chordal rupture is rarely reported in hypertrophic cardiomyopathy.
- The prevalence and characteristics of this event in large cohorts remain uncharacterized.
Purpose of the Study:
- To determine the prevalence of mitral valve chordal rupture in hypertrophic cardiomyopathy patients.
- To describe the clinical, echocardiographic, surgical, and histological features of affected individuals.
Main Methods:
- Retrospective review of patients with hypertrophic cardiomyopathy (2000-2010).
- Identification of mitral valve chordal rupture via echocardiography.
- Comparison with patients without chordal rupture.
Main Results:
- Six of 580 hypertrophic cardiomyopathy patients (1%) had mitral valve chordal rupture.
- Rupture involved the posterior mitral leaflet, often associated with systolic anterior motion and leaflet elongation.
- Pre-existing left ventricular outflow tract obstruction resolved post-rupture in surgically treated patients.
- Histology revealed myxomatous degeneration in all cases.
Conclusions:
- Mitral valve chordal rupture is an infrequent complication in hypertrophic cardiomyopathy.
- It primarily affects elderly patients with obstructive hypertrophic cardiomyopathy and posterior leaflet involvement.
- Severe mitral regurgitation necessitating surgery is a common outcome, with myxomatous degeneration as a potential underlying factor.
Background:
While occasional reports of mitral valve chordal rupture have been described in hypertrophic cardiomyopathy, the exact prevalence and characteristics of this event in a large medical cohort have not been reported.
Aim:
To assess the prevalence of mitral valve chordal rupture in hypertrophic cardiomyopathy and the clinical, echocardiographic, surgical and histological profiles of those patients.
Methods:
We searched for patients with mitral valve chordal rupture diagnosed by echocardiography among all electronic files of patients admitted to our centre for hypertrophic cardiomyopathy between 2000 and 2010.
Results:
Among 580 patients admitted for hypertrophic cardiomyopathy, six patients (1%, 5 men, age 68-71 years) presented with mitral valve chordal rupture, symptomatic in five cases, always involving the posterior mitral leaflet. In all cases, echocardiography before rupture showed mitral valve systolic anterior motion, with anterior (and not posterior) leaflet elongation compared with a random sample of patients with non-obstructive hypertrophic cardiomyopathy (P=0.006) (and similar to that observed in obstructive hypertrophic cardiomyopathy). Significant resting left ventricular outflow tract obstruction was always present before rupture and disappeared after rupture in the five cases requiring mitral valve surgery for severe mitral regurgitation. Histological findings were consistent with extensive myxomatous degeneration in all cases.
Conclusion:
Mitral valve chordal rupture is: infrequent in hypertrophic cardiomyopathy; occurs in aged patients with obstructive disease; involves, essentially, the posterior mitral leaflet; and causes, in general, severe mitral regurgitation requiring surgery. Myxomatous degeneration may be the substrate for rupture in these patients.
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