Untargeted Lipidomics in Fabry Disease of Urine Samples by Low-Resolution Flow Injection Mass Spectrometry (ESI(±)-LTQ MS)
Rafael Arruda Foletto, Augusto Santos Borges, LarissaCampos Motta, Marcos Valério Vieira Lyrio, Carolina Teles Baretto, Luciene Cristina Gastalho Campos, Paulo Roberto Filgueiras, Valério Garrone Barauna, Wanderson Romão

TL;DR
This study explores using urine samples and lipidomics with mass spectrometry to diagnose Fabry disease, a genetic disorder, with high accuracy.
Contribution
The novel use of urine samples and multivariate analysis in lipidomics for early diagnosis of Fabry disease is proposed.
Findings
Combining positive and negative ionization modes in PLS-DA achieved 92% accuracy in differentiating Fabry disease cases from controls.
Urine-based lipidomics combined with multivariate analysis is a promising tool for early diagnosis of Fabry disease.
The method enables improved healthcare outcomes through early detection of the disease.
Abstract
Background: Fabry disease (FD) is a lysosomal storage disease caused by genetic mutations related to the coding of the enzyme α-galactosidase A, which is responsible for the metabolism of glycosphingolipids such as globotriaosylceramide and globotriaosylsphingosine. The accumulation of these and other metabolites can occur in various types of cells and impair the functioning of multiple organs and systems, such as the heart, brain, and kidneys. However, with early diagnosis and appropriate therapeutic intervention, the clinical outcome can be significantly improved. This study aimed to analyze the performance of new diagnostic methods for FD using the broad field of lipidomics combined with multivariate analyses, proposing the use of urine as a specimen. Materials and Methods: urine samples were collected from patients with both confirmed (Case) and negative (Control) diagnoses of FD,…
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Taxonomy
TopicsLysosomal Storage Disorders Research · Metabolomics and Mass Spectrometry Studies · Metabolism and Genetic Disorders
