Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Sep 13;23(1):102.
doi: 10.1186/s12968-021-00797-2.

Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse

Affiliations

Myocardial extracellular volume by T1 mapping: a new marker of arrhythmia in mitral valve prolapse

Anna Giulia Pavon et al. J Cardiovasc Magn Reson. .

Abstract

Objectives: We aimed to evaluate the relationship between mitral annular disjunction (MAD) severity and myocardial interstitial fibrosis at the left ventricular (LV) base in patients with mitral valve prolapse (MVP), and to assess the association between severity of interstitial fibrosis and the occurrence of ventricular arrhythmic events.

Background: In MVP, MAD has been associated with myocardial replacement fibrosis and arrhythmia, but the importance of interstitial fibrosis remains unknown.

Methods: In this retrospective study, 30 patients with MVP and MAD (MVP-MAD) underwent cardiovascular magnetic resonance (CMR) with assessment of MAD length, late gadolinium enhancement (LGE), and basal segments myocardial extracellular volume (ECVsyn). The control group included 14 patients with mitral regurgitation (MR) but no MAD (MR-NoMAD) and 10 patients with normal CMR (NoMR-NoMAD). Fifteen MVP-MAD patients underwent 24 h-Holter monitoring.

Results: LGE was observed in 47% of MVP-MAD patients and was absent in all controls. ECVsyn was higher in MVP-MAD (30 ± 3% vs 24 ± 3% MR-NoMAD, p < 0.001 and vs 24 ± 2% NoMR-NoMAD, p < 0.001), even in MVP-MAD patients without LGE (29 ± 3% vs 24 ± 3%, p < 0.001 and vs 24 ± 2%, p < 0.001, respectively). MAD length correlated with ECVsyn (rho = 0.61, p < 0.001), but not with LGE extent. Four patients had history of out-of-hospital cardiac arrest; LGE and ECVsyn were equally performant to identify those high-risk patients, area under the receiver operating characteristic (ROC) curve 0.81 vs 0.83, p = 0.84). Among patients with Holter, 87% had complex ventricular arrhythmia. ECVsyn was above the cut-off value in all while only 53% had LGE.

Conclusion: Increase in ECVsyn, a marker of interstitial fibrosis, occurs in MVP-MAD even in the absence of LGE, and was correlated with MAD length and increased risk of out-of-hospital cardiac arrest. ECV should be includedin the CMR examination of MVP patients in an effort to better assess fibrous remodelling as it may provide additional value beyond the assessment of LGE in the arrhythmic risk stratification.

Keywords: Cardiovascular magnetic resonance; Interstitial fibrosis; Mitral annular disjunction; Mitral valve prolapse.

PubMed Disclaimer

Conflict of interest statement

Beyond the study’s interests, Dr. Le Bloa received a training scholarship from the SIPCA Foundation, Prilly, Switzerland. Prof Schwitter received research grants from Bayer Healthcare, Switzerland. Other authors have nothing to disclose.

Figures

Fig. 1
Fig. 1
A Cardiovascular magnetic resonance (CMR) 3 chambers cine image at end-systole for measurement of mitral annular disjunction (MAD) length. B, C Semi-automatic measurement of segmental pre-contrast (B) and post-contrast (C) T1 relaxation time of the basal left ventricular myocardium
Fig. 2
Fig. 2
Distribution of late gadolinium enhancement (LGE) positivity in patients with mitral valve prolapse (MVP) and MAD (n = 30). A anterior, AL anterolateral, IL inferolateral, I inferior, IS inferoseptal, AS anteroseptal
Fig. 3
Fig. 3
Pre-contrast T1 relaxation time measured in the six basal myocardial segments. The average T1 relaxation time is indicated in the center of each plot. Abbreviations: see Fig. 2
Fig. 4
Fig. 4
Extracellular volume (ECV) calculated in the six basal myocardial segments. The average ECV is indicated in the center of each plot. Abbreviations: see Fig. 2
Fig. 5
Fig. 5
Relation between MAD distance and parameters of myocardial fibrosis
Fig. 6
Fig. 6
Comparison of fibrosis parameters in patients with and without out-of-hospital cardiac arrest
Fig. 7
Fig. 7
Intra-observer reproducibility of pre-contrast T1 relaxation time (left hand panels) and extracellular volume (right hand panels) measurements
Fig. 8
Fig. 8
Inter-observer reproducibility of pre-contrast T1 relaxation time (left hand panels) and extracellular volume (right hand panels) measurements

References

    1. Nordhues BD, Siontis KC, Scott CG, et al. Bileaflet mitral valve prolapse and risk of ventricular dysrhythmias and death. J Cardiovasc Electrophysiol. 2016;27:463–468. doi: 10.1111/jce.12914. - DOI - PubMed
    1. Narayanan K, Uy-Evanado A, Teodorescu C, et al. Mitral valve prolapse and sudden cardiac arrest in the community. Heart Rhythm. 2016;13:498–503. doi: 10.1016/j.hrthm.2015.09.026. - DOI - PMC - PubMed
    1. Freed LA, Levy D, Levine RA, et al. Prevalence and clinical outcome of mitral-valve prolapse. N Engl J Med. 1999;341:1–7. doi: 10.1056/NEJM199907013410101. - DOI - PubMed
    1. Sriram CS, Syed FF, Ferguson ME, et al. Malignant bileaflet mitral valve prolapse syndrome in patients with otherwise idiopathic out-of-hospital cardiac arrest. J Am Coll Cardiol. 2013;62:222–230. doi: 10.1016/j.jacc.2013.02.060. - DOI - PubMed
    1. PerazzoloMarra M, Basso C, De Lazzari M, et al. Morphofunctional abnormalities of mitral annulus and arrhythmic mitral valve prolapse. Circ Cardiovasc Imaging. 2016;9:e005030. - PMC - PubMed

MeSH terms