Key result
Model with age, native T1 dispersion, and LV mass predicts 5-year cardiac events with ~0.77 c-statistic.
Why the study?
Risk stratification for adverse cardiac outcomes in patients with Fabry disease remains inadequate despite the leading cardiac manifestations causing death.
Cohort (n=200)
A parsimonious prognostic model using age, native myocardial T1 dispersion, and indexed left ventricular mass accurately predicts the 5-year risk of adverse cardiac outcomes in patients with Fabry disease.
BACKGROUND The cardiac manifestations of Fabry disease are the leading cause of death, but risk stratification remains inadequate. Identifying patients who are at risk of adverse cardiac outcome may facilitate more evidence-based treatment guidance. Contemporary cardiovascular cardiac magnetic resonance biomarkers have become widely adopted, but their prognostic value remains unclear. OBJECTIVES The objective of this study was to develop, internally validate, and evaluate the performance of, a prognostic model, including contemporary deep phenotyping, which can be used to generate individual risk estimates for adverse cardiac outcome in patients with Fabry disease. METHODS This longitudinal prospective cohort study consisted of 200 consecutive patients with Fabry disease undergoing clinical cardiac magnetic resonance. Median follow-up was 4.5 years (IQR: 2.7-6.3 years). Prognostic models were developed using Cox proportional hazards modeling. Outcome was a composite of adverse cardiac events. Model performance was evaluated. A risk calculator, which provides 5-year estimated risk of adverse cardiac outcome for individual patients, including men and women, was generated. RESULTS The highest performing, internally validated, parsimonious multivariable model included age, native myocardial T1 dispersion (SD of per voxel myocardial T1 relaxation times), and indexed left ventricular mass. Median optimism-adjusted c-statistic across 5 imputed model development data sets was 0.77 (95% CI: 0.70-0.84). Model calibration was excellent across the full risk profile. CONCLUSIONS This study developed and internally validated a risk prediction model that accurately predicts 5-year risk of adverse cardiac outcome for individual patients with Fabry disease, including men and women, which could easily be integrated into clinical care. External validation is warranted.
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Orsborne et al. (2022) conducted a cohort in Fabry disease (n=200). Prognostic model including age, native myocardial T1 dispersion, and indexed left ventricular mass was evaluated on Composite of adverse cardiac events (c-statistic 0.77, 95% CI 0.70-0.84). A parsimonious multivariable model including age, native myocardial T1 dispersion, and indexed left ventricular mass accurately predicted 5-year risk of adverse cardiac outcomes with a c-statistic of 0.77.
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