Reduced global longitudinal strain as a marker for early detection of Fabry cardiomyopathy

Dai-Yin Lu1,2,3,4, Wei-Ming Huang2,3,4, Wei-Ting Wang2,3

  • 1Division of General Medicine, Department of Medicine, Taipei Veterans General Hospital, 201, Section 2, Shipai Road, Taipei 11217, Taiwan.

Insights

Myocardial deformation analysis, specifically global longitudinal strain (GLS), can detect early Fabry cardiomyopathy (FC) before left ventricular hypertrophy (LVH) develops. This technique offers a sensitive marker for preclinical FC.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Genetics

Background:

  • Fabry cardiomyopathy (FC) is a progressive condition characterized by left ventricular hypertrophy (LVH).
  • Conventional echocardiography often fails to detect preclinical FC before LVH onset.
  • Early detection of FC is crucial for timely intervention and management.

Purpose of the Study:

  • To evaluate the utility of myocardial deformation analysis in detecting preclinical Fabry cardiomyopathy.
  • To determine if reduced global longitudinal strain (GLS) can serve as an early marker for FC before LVH development.

Main Methods:

  • Prospective enrollment of 160 patients with mutated genes (86 without LVH, 74 with LVH) and 33 healthy controls.
  • Performance of standard echocardiography, Doppler, tissue Doppler, and deformation analysis.
  • Comparison of cardiac parameters, including GLS, between groups.

Main Results:

  • Global longitudinal strain (GLS) significantly deteriorated with the progression of LVH.
  • Patients with Fabry cardiomyopathy but without LVH showed reduced GLS compared to healthy subjects.
  • Reduced GLS and regional longitudinal strains were observed even before overt LVH in FC patients.

Conclusions:

  • Reduced global longitudinal strain (GLS) is a potential early indicator of Fabry cardiomyopathy.
  • Myocardial deformation analysis can identify preclinical FC, preceding the development of left ventricular hypertrophy (LVH).
  • This imaging technique may aid in earlier diagnosis and management of Fabry cardiomyopathy.
Abstract

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