TY - JOUR A1 - García-Consuegra, Inés AU - Asensio Peña, Sara AU - Garrido Moraga, Rocío AU - Pinós, Tomás AU - Domínguez González, Cristina AU - Santalla Hernández, Alfredo AU - Nogales-Gadea, Gisela AU - Serrano Lorenzo, Pablo AU - Lucía Mulas, Alejandro AU - Martín Casanueva, Miguel Ángel AU - Et al. T1 - Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis Y1 - 2022 SN - 1422-0067 UR - http://hdl.handle.net/11268/11291 AB - Glycogen storage disease type V (GSDV, McArdle disease) is a rare genetic myopathy caused by deficiency of the muscle isoform of glycogen phosphorylase (PYGM). This results in a block in the use of muscle glycogen as an energetic substrate, with subsequent exercise intolerance. The pathobiology of GSDV is still not fully understood, especially with regard to some features such as persistent muscle damage (i.e., even without prior exercise). We aimed at identifying potential muscle protein biomarkers of GSDV by analyzing the muscle proteome and the molecular networks associated with muscle dysfunction in these patients. Muscle biopsies from eight patients and eight healthy controls showing none of the features of McArdle disease, such as frequent contractures and persistent muscle damage, were studied by quantitative protein expression using isobaric tags for relative and absolute quantitation (iTRAQ) followed by artificial neuronal networks (ANNs) and topology analysis. Protein candidate validation was performed by Western blot. Several proteins predominantly involved in the process of muscle contraction and/or calcium homeostasis, such as myosin, sarcoplasmic/endoplasmic reticulum calcium ATPase 1, tropomyosin alpha-1 chain, troponin isoforms, and alpha-actinin-3, showed significantly lower expression levels in the muscle of GSDV patients. These proteins could be potential biomarkers of the persistent muscle damage in the absence of prior exertion reported in GSDV patients. Further studies are needed to elucidate the molecular mechanisms by which PYGM controls the expression of these proteins. KW - Enfermedad del almacenamiento de glucógeno tipo V KW - Metabolismo KW - Enfermedad cardiovascular KW - Genética humana LA - eng ER -