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

Herzschrittmacherther Elektrophysiol. 2018 Mar;29(1):43-47. doi: 10.1007/s00399-017-0544-9. Epub 2017 Dec 12.


In the healthy heart, physiological heterogeneities in structure and in electrical and mechanical activity are crucial for normal, efficient excitation and pumping. Alterations of heterogeneity have been linked to arrhythmogenesis in various cardiac disorders such as long QT syndrome (LQTS). This inherited arrhythmia disorder is caused by mutations in different ion channel genes and is characterized by (heterogeneously) prolonged cardiac repolarization and increased risk for ventricular tachycardia, syncope and sudden cardiac death. Cardiac electrical and mechanical function are not independent of each other but interact in a bidirectional manner by electromechanical and mechano-electrical coupling. Therefore, changes in either process will affect the other. Recent experimental and clinical evidence suggests that LQTS, which is primarily considered an "electrical" disorder, also exhibits features of disturbed mechanical function and heterogeneity, which in turn appears to correlate with the risk of arrhythmia in the individual patient. In this review, we give a short overview of the current knowledge about physiological and pathological, long QT-related electrical and mechanical heterogeneity in the heart. Also, their respective roles for future risk prediction approaches in LQTS are discussed.

Keywords: Arrhythmogenesis; Electromechanical interaction; Heart diseases; Ion channels; Risk stratification.

Publication types

  • Review

MeSH terms

  • Biomechanical Phenomena / genetics
  • Biomechanical Phenomena / physiology
  • DNA Mutational Analysis
  • Death, Sudden, Cardiac / etiology
  • Electrocardiography*
  • Electrophysiological Phenomena / genetics
  • Electrophysiological Phenomena / physiology
  • Humans
  • Ion Channels / genetics
  • Ion Channels / physiology
  • Long QT Syndrome / genetics
  • Long QT Syndrome / physiopathology*
  • Myocardial Contraction / genetics
  • Myocardial Contraction / physiology
  • Risk Assessment
  • Syncope / genetics
  • Syncope / physiopathology
  • Tachycardia, Ventricular / genetics
  • Tachycardia, Ventricular / physiopathology


  • Ion Channels