Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy Cycles

Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the <i>GLA</i> gene encoding the α-galactosidase A enzyme. This enzyme cleaves the last sugar unit of glycosphingolipids, including globotriaosylceramide (Gb<sub>3</sub>), globotriaosylsphingosine...

Full description

Bibliographic Details
Main Authors: Michel Boutin, Pamela Lavoie, Iskren Menkovic, Amanda Toupin, Mona Abaoui, Maha Elidrissi-Elawad, Marie-Françoise Arthus, Carole Fortier, Claudia Ménard, Bruno Maranda, Daniel G. Bichet, Christiane Auray-Blais
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/17/6114
Description
Summary:Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the <i>GLA</i> gene encoding the α-galactosidase A enzyme. This enzyme cleaves the last sugar unit of glycosphingolipids, including globotriaosylceramide (Gb<sub>3</sub>), globotriaosylsphingosine (lyso-Gb<sub>3</sub>), and galabiosylceramide (Ga<sub>2</sub>). Enzyme impairment leads to substrate accumulation in different organs, vascular endothelia, and biological fluids. Enzyme replacement therapy (ERT) is a commonly used treatment. Urinary analysis of Gb<sub>3</sub> isoforms (different fatty acid moieties), as well as lyso-Gb<sub>3</sub> and its analogues, is a reliable way to monitor treatment. These analogues correspond to lyso-Gb<sub>3</sub> with chemical modifications on the sphingosine moiety (−C<sub>2</sub>H<sub>4</sub>, −C<sub>2</sub>H<sub>4</sub>+O, −H<sub>2</sub>, −H<sub>2</sub>+O, +O, +H<sub>2</sub>O<sub>2</sub>, and +H<sub>2</sub>O<sub>3</sub>). The effects of sample collection time on urinary biomarker levels between ERT cycles were not previously documented. The main objective of this project was to analyze the aforementioned biomarkers in urine samples from seven Fabry disease patients (three treated males, three treated females, and one ERT-naïve male) collected twice a day (morning and evening) for 42 days (three ERT cycles). Except for one participant, our results show that the biomarker levels were generally more elevated in the evening. However, there was less variability in samples collected in the morning. No cyclic variations in biomarker levels were observed between ERT infusions.
ISSN:1661-6596
1422-0067