Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7

• Published in: Biomolecules (Basel, Switzerland) Vol. 10; no. 3; p. 390
• Main Authors: Nambo-Venegas, Rafael, Valdez-Vargas, Claudia, Cisneros, Bulmaro, Palacios-González, Berenice, Vela-Amieva, Marcela, Ibarra-González, Isabel, Cerecedo-Zapata, César M, Martínez-Cruz, Emilio, Cortés, Hernán, Reyes-Grajeda, Juan P, Magaña, Jonathan J
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 03.03.2020; MDPI
• Subjects: Adult; Amino acids; Amino Acids - blood; biomarkers; Biomarkers - blood; cag repeats; Carnitine - analogs & derivatives; Carnitine - blood; Cerebellar ataxia; Female; Health aspects; Humans; Male; metabolic pathways; metabolomics; Middle Aged; mitochondrial disease; Physiological aspects; polyglutamine disease; spinocerebellar ataxia 7; Spinocerebellar Ataxias - blood; Mexico; spinocerebellar ataxia 7; metabolomics; biomarkers; CAG repeats; metabolic pathways; mitochondrial disease; polyglutamine disease
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom10030390

Spinocerebellar ataxia type 7 (SCA7), a neurodegenerative disease characterized by cerebellar ataxia and retinal degeneration, is caused by an abnormal CAG repeat expansion in the gene coding region. The onset and severity of SCA7 are highly variable between patients, thus identification of sensitive biomarkers that accurately diagnose the disease and monitoring its progression are needed. With the aim of identified SCA7-specific metabolites with clinical relevance, we report for the first time, to the best of our knowledge, a metabolomics profiling of circulating acylcarnitines and amino acids in SCA7 patients. We identified 21 metabolites with altered levels in SCA7 patients and determined two different sets of metabolites with diagnostic power. The first signature of metabolites (Valine, Leucine, and Tyrosine) has the ability to discriminate between SCA7 patients and healthy controls, while the second one (Methionine, 3-hydroxytetradecanoyl-carnitine, and 3-hydroxyoctadecanoyl-carnitine) possess the capability to differentiate between early-onset and adult-onset patients, as shown by the multivariate model and ROC analyses. Furthermore, enrichment analyses of metabolic pathways suggest alterations in mitochondrial function, energy metabolism, and fatty acid beta-oxidation in SCA7 patients. In summary, circulating SCA7-specific metabolites identified in this study could serve as effective predictors of SCA7 progression in the clinics, as they are sampled in accessible biofluid and assessed by a relatively simple biochemical assay.