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Published on: June 20, 2014
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.
Objective:
Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac involvement in Fabry disease. We aimed to gain further insight into this by assessing a cohort of Fabry patients using CMR.
Methods/Results:
Fifty genotype-positive Fabry subjects (age 45±2 years; 50% male) referred for CMR and 39 matched controls (age 40±2 years; 59% male) were recruited. Patients had a mean Mainz severity score index of 15±2 (range 0-46), reflecting an overall mild degree of disease severity. Compared with controls, Fabry subjects had a 34% greater left ventricular mass (LVM) index (82±5 vs 61±2 g/m(2), p=0.001) and had a significantly greater papillary muscle contribution to total LVM (13±1 vs 6±0.5%, p<0.001), even in the absence of left ventricular hypertrophy (LVH). Late gadolinium enhancement (LGE) was present in 15 Fabry subjects (9/21 males and 6/23 females). The most common site for LGE was the basal inferolateral wall (93%, 14/15). There was a positive association between LVM index and LGE. Despite this, there were two males and three females with no LVH that displayed LGE. Of Fabry subjects who were not on enzyme replacement therapy at enrolment (n=28), six were reclassified as having cardiac involvement (four LVH-negative/LGE-positive, one LVH-positive/LGE-positive and one LVH-positive/LGE-negative).
Conclusions:
CMR was able to detect cardiac involvement in 48% of this Fabry cohort, despite the overall mild disease phenotype of the cohort. Of those not on ERT, 21% were reclassified as having cardiac involvement allowing improved risk stratification and targeting of therapy.
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