Arrhythmic risk profile in mitral valve prolapse: A systematic review and metanalysis of 1715 patients

Author:

Pistelli Lorenzo1ORCID,Vetta Giampaolo1ORCID,Parlavecchio Antonio1ORCID,Crea Pasquale1,Parisi Francesca1,Magnocavallo Michele2,Caminiti Rodolfo1,Frea Simone3,Vairo Alessandro3,Desalvo Paolo45ORCID,Faletti Riccardo6,Gatti Marco6ORCID,Dattilo Giuseppe1,Parollo Matteo7ORCID,Di Cori Andrea7,Bongiorni Maria Grazia7,De Santis Giulia1,Borgi Marco1,Franzino Marco1,Licordari Roberto1,Zucchelli Giulio7,Rocca Giovanni Domenico Della8,Giustetto Carla34

Affiliation:

1. Cardiology Unit, Department of Clinical and Experimental Medicine University of Messina Messina Italy

2. Arrhythmology Unit S. Giovanni Calibita Hospital, Cardiology Division Rome Italy

3. Cardiovascular and Thoracic Department "Citta della Salute e della Scienza" Hospital, Division of Cardiology Turin Italy

4. Department of Medical Sciences University of Turin Turin Italy

5. Cardiology Unit, Ospedale Santa Croce e Carle Cuneo Italy

6. Radiology Unit, Città della Salute e della Scienza Hospital University of Turin Turin Italy

7. Second Division of Cardiology Azienda Ospedaliero Universitaria Pisana Pisa Italy

8. Heart Rhythm Management Centre, Postgraduate Program in Cardiac Electrophysiology and Pacing, European Reference Networks Guard‐Heart Universitair Ziekenhuis Brussel‐Vrije Universiteit Brussel Brussels Belgium

Abstract

AbstractIntroductionMitral valve prolapse (MVP) is a common clinical condition in the general population. A subgroup of patients with MVP may experience ventricular arrhythmias and sudden cardiac death (“arrhythmic mitral valve prolapse” [AMVP]) but how to stratify arrhythmic risk is still unclear. Our meta‐analysis aims to identify predictive factors for arrhythmic risk in patients with MVP.MethodsWe systematically searched Medline, Cochrane, Journals@Ovid, Scopus electronic databases for studies published up to December 28, 2022 and comparing AMVP and nonarrhythmic mitral valve prolapse (NAMVP) for what concerns history, electrocardiographic, echocardiographic and cardiac magnetic resonance features. The effect size was estimated using a random‐effect model as odds ratio (OR) and mean difference (MD).ResultsA total of 10 studies enrolling 1715 patients were included. Late gadolinium enhancement (LGE) (OR: 16.67; p = .005), T‐wave inversion (TWI) (OR: 2.63; p < .0001), bileaflet MVP (OR: 1.92; p < .0001) and mitral anulus disjunction (MAD) (OR: 2.60; p < .0001) were more represented among patients with AMVP than in NAMVP. Patients with AMVP were shown to have longer anterior mitral leaflet (AML) (MD: 2.63 mm; p < .0001), posterior mitral leaflet (MD: 2.96 mm; p < .0001), thicker AML (MD: 0.49 mm; p < .0001), longer MAD length (MD: 1.24 mm; p < .0001) and higher amount of LGE (MD: 1.41%; p < .0001) than NAMVP. AMVP showed increased mechanical dispersion (MD: 8.04 ms; 95% confidence interval: 5.13–10.96; p < .0001) compared with NAMVP.ConclusionsOur meta‐analysis proved that LGE, TWI, bileaflet MVP, and MAD are predictive factors for arrhythmic risk in MVP patients.

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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