Abstract

Previous cross-sectional studies reported a high prevalence of ascending aorta dilations/aneurysms in male adults with Fabry disease, independently of cardiovascular risk factors. To characterise the remodelling of the ascending aorta in classic Fabry disease under long-term enzyme replacement therapy. Diameter of the ascending aorta was measured with magnetic resonance imaging at the sino-tubular junction (STJ), and proximal (pAsAo), and distal ascending aorta (dAsAo) at baseline, and after 5 and 10 years of enzyme replacement therapy in 15 adult Fabry patients (10 males; 5 females). Over a mean follow-up of 9.5 years, the annual expansion rates measured in 10 males with Fabry disease were 0.41 ± 0.16, 0.36 ± 0.25 and 0.41 ± 0.26 mm/y at the STJ, pAsAo and dAsAo, respectively. Expansion rate at the pAsAo level in male patients was significantly higher than the expected expansion projected from theoretical normal values: 0.36 ± 0.25 vs 0.13 ± 0.05, p = 0.017. In 5 females, the annual expansion rates at the STJ, pAsAo and dAsAo were 0.14 ± 0.11, 0.21 ± 0.18 and 0.26 ± 0.24 mm/y, respectively. There was no significant difference from the projected normal expansion rate at the level of the pAsAo: 0.21 ± 0.18 vs 0.13 ± 0.04, p = 0.39. Our data suggest that the remodelling of the ascending aorta is more pronounced in male patients with Fabry disease under long-term enzyme replacement therapy compared with the progression observed in a large population study.

Highlights

  • Fabry disease is a rare X-linked disorder caused by deficiency of the lysosomal enzyme alpha-galactosidase A (α-Gal A)

  • Over a mean follow-up of 9.5 years, the annual expansion rates measured in 10 males with Fabry disease were 0.41 ± 0.16, 0.36 ± 0.25 and 0.41 ± 0.26 mm/y at the sino-tubular junction (STJ), proximal ascending aorta (pAsAo) and distal ascending aorta (dAsAo), respectively

  • Our data suggest that the remodelling of the ascending aorta is more pronounced in male patients with Fabry disease under long-term enzyme replacement therapy compared with the progression observed in a large population study

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Summary

Introduction

Fabry disease is a rare X-linked disorder caused by deficiency of the lysosomal enzyme alpha-galactosidase A (α-Gal A) This defect leads to progressive accumulation of glycosphingolipids (GSL) in many tissues and organs, and in particular in endothelial and vascular smooth muscle cells (VSMC) of the arterial tree [1]. A high prevalence of asymptomatic dilation and aneurysms of the proximal ascending aorta (pAsAo), which occurred at a younger age compared with the general population, was previously reported in male patients with the classic form of Fabry disease [7]. The aim of the present study was to compare the remodelling of the ascending aorta in adult patients with Fabry disease under long-term ERT with the normal aortic remodelling computed from large population data

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