Abstract

BackgroundVarious electrocardiographic (ECG) indices have been shown to be useful for early recognition and staging of cardiac involvement in Fabry Disease (FD). However, many of them lack acceptable sensitivity and specificity. We assessed the value of automated ECG measures to discriminate between pre-hypertrophic FD and healthy individuals. Methods and resultsNormal ECGs from 1496 healthy individuals (57.4% male, age 37.4 ± 13 years) were compared to those of 142 FD patients without LVH (37.3% male, age 41.5 ± 18 years). All ECGs were analyzed centrally and a total of 429 automated ECG measures per individual were included for step-wise analysis. The Cramer V statistic was first used to pick out those parameters which were helpful in discriminating between the two groups and a final selection was made by using two models, namely the FLD (Fisher Linear Discrimination) and the Logistic model, to optimise diagnostic performance for the detection of cardiac involvement in FD patients vs. specificity in healthy individuals.The three-step statistical analysis identified 9 ECG parameters as most significant for the discrimination between the groups. The combined discriminant score yielded 64% sensitivity and 97% specificity for correct classification of FD patients in the test sample with a logistic area under curve of the ROC analysis of 0.97. ConclusionThe combination of automated ECG measures identified via a stepwise statistical approach may be useful for detection of FD patients in the pre-hypertrophic stage. These data are promising for screening purposes in the very early stages of FD cardiomyopathy and warrant prospective confirmation.

Highlights

  • Fabry Disease (FD) is an inherited X-linked, recessive lysosomal storage disease caused by deficient activity of the lysosomal enzyme α-galactosidase A [1]

  • Organ involvement at the time of diagnosis may already be characterized by extensive left ventricular hypertrophy (LVH) and myocardial fibrosis, i.e. fully-fledged FD cardiomyopathy, which is irreversible and unresponsive to enzyme replacement therapy (ERT) [2,5]

  • The 4/8 QRS spatial velocity was lower in the FD group (93.2 μV/ms vs. 130.1 μV/ms, p = 0.0001)

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Summary

Introduction

Fabry Disease (FD) is an inherited X-linked, recessive lysosomal storage disease caused by deficient activity of the lysosomal enzyme α-galactosidase A [1]. The Cramer V statistic was first used to pick out those parameters which were helpful in discriminating between the two groups and a final selection was made by using two models, namely the FLD (Fisher Linear Discrimination) and the Logistic model, to optimise diagnostic performance for the detection of cardiac involvement in FD patients vs specificity in healthy individuals. Conclusion: The combination of automated ECG measures identified via a stepwise statistical approach may be useful for detection of FD patients in the pre-hypertrophic stage. These data are promising for screening purposes in the very early stages of FD cardiomyopathy and warrant prospective confirmation

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