*Christina Attenhofer Jost,1 Matthias Greutmann,2 Heidi M. Connolly,3 Barbara Naegeli,1 Anja Faeh-Gunz,1 Christoph Scharf,1 Reto Candinas,1 Emanuela Valsangiacomo Buechel,4 Roland Weber,4 Christian Binggeli,1 Olaf Franzen,1 Argelia Medeiros-Domingo5
1. Cardiovascular Centre Zurich, Klinik Im Park, Zurich, Switzerland
2. University Heart Centre, Division of Cardiology, University Hospital Zurich, Zurich, Switzerland
3. Cardiovascular Division, Mayo Clinic, Rochester, Minnesota, USA
4. Division of Cardiology, University Children’s Hospital, Zurich, Zurich, Switzerland
5. Division of Cardiology, Inselspital, Bern, Switzerland
*Correspondence to email@example.com
Disclosure: No potential conflict of interest.
Received: 18.11.14 Accepted: 06.01.15
Citation: EMJ Cardiol. 2015;3:30-37.
In most patients with mitral valve prolapse (MVP) without severe mitral regurgitation (MR), left ventricular (LV) function is preserved. There are, however, patients with MVP who have unexplained LV dilatation and/or decreased LV function. An association between MVP and sudden cardiac death has also been reported. LV size and function may be affected by the type of MVP, severity of regurgitation, and cause of MVP (myxomatous degeneration versus fibroelastic deficiency). There is increasing evidence suggesting an intrinsic cardiomyopathy associated with MVP. The cardiomyopathy associated with MVP can also affect the right ventricle (RV). Although the impact on ventricular dimensions and function are usually subtle, these abnormalities can affect clinical and echocardiographic estimation of the severity of MR and may thus have an impact on therapeutic decisions. Particularly in patients with the most extreme forms of MVP (Barlow disease), and in patients with Marfan syndrome or other connective tissue disorders, a cardiomyopathy affecting the LV and RV may thus occur occasionally. A better understanding of LV impairment associated with MVP is important for risk assessment and clinical decision-making.