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      Diffuse myocardial fibrosis in patients with mitral valve prolapse and ventricular arrhythmia

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          Abstract

          Objective

          We aimed to investigate the association of diffuse myocardial fibrosis by cardiac magnetic resonance (CMR) T 1 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 T 1 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 T 1 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 T 1 times, with LVEF and LV end-diastolic volume being the strongest (p=0.005, p=0.008 and p=0.045, respectively; model adjusted R 2=0.30). Patients with MVP with ComVA had significantly shorter postcontrast T 1 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 T 1 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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          Author and article information

          Journal
          9602087
          20297
          Heart
          Heart
          Heart (British Cardiac Society)
          1355-6037
          1468-201X
          2 November 2016
          11 August 2016
          February 2017
          01 February 2018
          : 103
          : 3
          : 204-209
          Affiliations
          [1 ]Cardiovascular Division, Department of Medicine, Harvard-Thorndike Electrophysiology Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
          [2 ]Department of Medicine, Cardiovascular Division, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
          [3 ]Division of Cardiology, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Brazil
          [4 ]Department of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
          [5 ]Department of Medicine, Division of Cardiology, University of California, San Francisco, California, USA
          Author notes
          Correspondence to Dr Francesca N Delling, University of California, San Francisco, 555 Mission Bay Blvd South, Room S352C, San Francisco, CA 94158, USA; Francesca.Delling@ 123456ucsf.edu
          Article
          PMC5237392 PMC5237392 5237392 nihpa826855
          10.1136/heartjnl-2016-309303
          5237392
          27515954
          38220a86-c582-4a72-9e2c-1dbdaedc1bc9
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