Unveiling Functional Impairment in Fabry Disease: The Role of Peripheral vs. Cardiac Mechanisms
Geza Halasz, Chiara Lanzillo, Raffaella Mistrulli, Emanuele Canali, Elisa Fedele, Paolo Ciacci, Federica Onorato, Guido Giacalone, Giovanni Nardecchia, Domenico Gabrielli, Federica Re

TL;DR
This study finds that Fabry disease patients show early functional impairments not fully captured by standard heart imaging, suggesting broader systemic issues.
Contribution
The study introduces CPET as a novel tool to detect early systemic limitations in Fabry disease beyond cardiac imaging.
Findings
CPET revealed reduced peak VO2 and early anaerobic threshold in AFD patients despite normal diastolic indices.
Impaired global longitudinal strain and mildly reduced VO2/watt ratio suggest peripheral limitations in AFD.
Functional impairment in AFD is common even with mild cardiac involvement.
Abstract
Background: Anderson–Fabry disease (AFD) is a progressive lysosomal storage disorder characterized by systemic glycosphingolipid accumulation. While cardiac imaging plays a central role in disease monitoring, the relationship between structural myocardial changes and exercise capacity remains incompletely defined. This study aimed to evaluate functional impairment in AFD patients using cardiopulmonary exercise testing (CPET) and to determine whether limitations are primarily cardiac or extracardiac in origin. Methods: Thirty-one patients with genetically confirmed AFD were retrospectively enrolled from two tertiary centers. All underwent baseline clinical assessment, resting transthoracic echocardiography (TTE), spirometry, and symptom-limited CPET using a cycle ergometer and a 10 W/min ramp protocol. Echocardiographic parameters included the LVEF, global longitudinal strain (GLS), E/e′…
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Taxonomy
TopicsLysosomal Storage Disorders Research · Mitochondrial Function and Pathology · Trypanosoma species research and implications
