Literature DB >> 28479515

Phase-contrast magnet resonance imaging reveals regional, transmural, and base-to-apex dispersion of mechanical dysfunction in patients with long QT syndrome.

Johannes Brado1, Markus J Dechant2, Marius Menza3, Adriana Komancsek3, Corinna N Lang1, Heiko Bugger1, Daniela Foell1, Bernd A Jung4, Brigitte Stiller2, Christoph Bode1, Katja E Odening5.   

Abstract

BACKGROUND: Regional dispersion of prolonged repolarization is a hallmark of long QT syndrome (LQTS). We have also revealed regional heterogeneities in mechanical dysfunction in transgenic rabbit models of LQTS.
OBJECTIVE: In this clinical pilot study, we investigated whether patients with LQTS exhibit dispersion of mechanical/diastolic dysfunction.
METHODS: Nine pediatric patients with genotyped LQTS (12.2 ± 3.3 years) and 9 age- and sex-matched healthy controls (10.6 ± 1.5 years) were subjected to phase-contrast magnetic resonance imaging to analyze radial (Vr) and longitudinal (Vz) myocardial velocities during systole and diastole in the left ventricle (LV) base, mid, and apex. Twelve-lead electrocardiograms were recorded to assess the heart rate-corrected QT (QTc) interval.
RESULTS: The QTc interval was longer in patients with LQTS than in controls (469.1 ± 39.4 ms vs 417.8 ± 24.4 ms; P < .01). Patients with LQTS demonstrated prolonged radial and longitudinal time-to-diastolic peak velocities (TTP), a marker for prolonged contraction duration, in the LV base, mid, and apex. The longer QTc interval positively correlated with longer time-to-diastolic peak velocities (correlation coefficient 0.63; P < .01). Peak diastolic velocities were reduced in LQTS in the LV mid and apex, indicating impaired diastolic relaxation. In patients with LQTS, regional (TTPmax-min) and transmural (TTPVz-Vr) dispersion of contraction duration was increased in the LV apex (TTPVz_max-min: 38.9 ± 25.5 ms vs 20.2 ± 14.7 ms; P = .07; TTPVz-Vr: -21.7 ± 14.5 ms vs -8.7 ± 11.3 ms; P < .05). The base-to-apex longitudinal relaxation sequence was reversed in patients with LQTS compared with controls (TTPVz_base-apex: 14.4 ± 14.9 ms vs -10.1 ± 12.7 ms; P < .01).
CONCLUSION: Patients with LQTS exhibit diastolic dysfunction with reduced diastolic velocities and prolonged contraction duration. Mechanical dispersion is increased in LQTS with an increased regional and transmural dispersion of contraction duration and altered apicobasal longitudinal relaxation sequence. LQTS is an electromechanical disorder, and phase-contrast magnetic resonance imaging Heterogeneity in mechanical dysfunction enables a detailed assessment of mechanical consequences of LQTS.
Copyright © 2017 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Diastolic dysfunction; Dispersion of contraction duration; Heterogeneity in mechanical dysfunction; LQTS; Magnet resonance imaging

Mesh:

Substances:

Year:  2017        PMID: 28479515     DOI: 10.1016/j.hrthm.2017.04.045

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  9 in total

Review 1.  Report on the Ion Channel Symposium : Organized by the German Cardiac Society Working Group on Cellular Electrophysiology (AG 18).

Authors:  Niels Voigt; Fleur Mason; Dierk Thomas
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2018-01-08

2.  Impact of age and cardiac disease on regional left and right ventricular myocardial motion in healthy controls and patients with repaired tetralogy of fallot.

Authors:  Alexander Ruh; Roberto Sarnari; Haben Berhane; Kenny Sidoryk; Kai Lin; Ryan Dolan; Arleen Li; Michael J Rose; Joshua D Robinson; James C Carr; Cynthia K Rigsby; Michael Markl
Journal:  Int J Cardiovasc Imaging       Date:  2019-02-04       Impact factor: 2.357

Review 3.  Electromechanical heterogeneity in the heart : A key to long QT syndrome?

Authors:  F F Dressler; J Brado; K E Odening
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2017-12-12

Review 4.  Role of ion channels in heart failure and channelopathies.

Authors:  Ann-Kathrin Rahm; Patrick Lugenbiel; Patrick A Schweizer; Hugo A Katus; Dierk Thomas
Journal:  Biophys Rev       Date:  2018-07-17

5.  A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children.

Authors:  Arja Suzanne Vink; Irene M Kuipers; Rianne H A C M De Bruin-Bon; Arthur A M Wilde; Nico A Blom; Sally-Ann B Clur
Journal:  Pediatr Cardiol       Date:  2018-05-22       Impact factor: 1.655

6.  Exercise worsening of electromechanical disturbances: A predictor of arrhythmia in long QT syndrome.

Authors:  Dafni Charisopoulou; George Koulaouzidis; Annika Rydberg; Henein Y Michael
Journal:  Clin Cardiol       Date:  2018-12-22       Impact factor: 2.882

7.  Reversed Apico-Basal Myocardial Relaxation Sequence During Exercise in Long QT Syndrome Mutations Carriers With History of Previous Cardiac Events.

Authors:  Dafni Charisopoulou; George Koulaouzidis; Annika Rydberg; Michael Y Henein
Journal:  Front Physiol       Date:  2022-02-07       Impact factor: 4.566

8.  Genotype-Specific ECG-Based Risk Stratification Approaches in Patients With Long-QT Syndrome.

Authors:  Marina Rieder; Paul Kreifels; Judith Stuplich; David Ziupa; Helge Servatius; Luisa Nicolai; Alessandro Castiglione; Christiane Zweier; Babken Asatryan; Katja E Odening
Journal:  Front Cardiovasc Med       Date:  2022-07-14

Review 9.  Electromechanical reciprocity and arrhythmogenesis in long-QT syndrome and beyond.

Authors:  Katja E Odening; Henk J van der Linde; Michael J Ackerman; Paul G A Volders; Rachel M A Ter Bekke
Journal:  Eur Heart J       Date:  2022-08-21       Impact factor: 35.855

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.