Cardiac involvement in genotype-positive Fabry disease patients assessed by cardiovascular MR

Rebecca Kozor1, Stuart M Grieve2, Michel C Tchan3

  • 1North Shore Heart Research Group, Kolling Institute of Medical Research, University of Sydney, Sydney, New South Wales, Australia Sydney Translational Imaging Laboratory, Sydney Medical School and Charles Perkins Centre, University of Sydney, Sydney, New South Wales, Australia Department of Cardiology, Royal North Shore Hospital, Sydney, New South Wales, Australia.

Insights

Cardiac magnetic resonance (CMR) detects cardiac involvement in Fabry disease, even with mild symptoms. This imaging can reclassify patients, improving risk assessment and treatment targeting for Fabry disease.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Genetics

Background:

  • Fabry disease is a rare genetic disorder that can affect the heart.
  • Early detection of cardiac involvement is crucial for managing Fabry disease.
  • Cardiac magnetic resonance (CMR) shows promise for identifying cardiac issues in Fabry patients.

Purpose of the Study:

  • To assess the utility of CMR in detecting cardiac involvement in a cohort of Fabry disease patients.
  • To investigate cardiac structural and functional changes in Fabry disease using CMR.
  • To evaluate the impact of CMR findings on risk stratification and treatment decisions.

Main Methods:

  • Recruited 50 genotype-positive Fabry subjects and 39 matched controls for CMR.
  • Assessed left ventricular mass (LVM) index and papillary muscle contribution to LVM.
  • Utilized late gadolinium enhancement (LGE) to detect myocardial fibrosis.

Main Results:

  • Fabry subjects showed significantly greater LVM index and papillary muscle contribution compared to controls.
  • Late gadolinium enhancement (LGE) was observed in 15 Fabry subjects, predominantly in the basal inferolateral wall.
  • A positive association was found between LVM index and LGE, with some patients showing LGE without left ventricular hypertrophy (LVH).

Conclusions:

  • CMR detected cardiac involvement in 48% of the Fabry cohort, including those with mild disease phenotypes.
  • In patients not on enzyme replacement therapy (ERT), 21% were reclassified as having cardiac involvement based on CMR findings.
  • CMR findings aid in improved risk stratification and targeted therapy for Fabry disease patients.
Abstract

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