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dc.creatorMartínez-Lara, Antonioes
dc.creatorMoreno-Fernández, Ana Maríaes
dc.creatorJiménez-Guerrero, Maripazes
dc.creatorDíaz-López, Claudiaes
dc.creatorMiguel Rodríguez, Manuel dees
dc.creatorCotán, Davides
dc.creatorSánchez-Alcázar, José Antonioes
dc.date.accessioned2023-02-06T14:55:48Z
dc.date.available2023-02-06T14:55:48Z
dc.date.issued2020
dc.identifier.citationMartínez-Lara, A., Moreno-Fernández, A.M., Jiménez-Guerrero, M., Díaz-López, C., Miguel Rodríguez, M.d., Cotán, D. y Sánchez-Alcázar, J.A. (2020). Mitochondrial imbalance as a new approach to the study of fibromyalgia. Open Access Rheumatology: Research and Reviews, 12, 175-185. https://doi.org/10.2147/OARRR.S257470.
dc.identifier.issn1179-156Xes
dc.identifier.urihttps://hdl.handle.net/11441/142478
dc.description.abstractBackground: Fibromyalgia (FM) is a common chronic pain disease, whose pathogenic mechanism still remains elusive. Oxidative stress markers and impaired bioenergetics homeostasis have been proposed as relevant events in the pathogenesis of the disease. Hence, the aim of the study is to analyse the potential biomarkers of mitochondrial imbalance in FM patients along with coenzyme Q10 (CoQ10) as a possible treatment. Methods: The symptomatology of patients was recorded with an adaption of the Fibromyalgia Impact Questionnaire (FIQ). Mitochondrial imbalance was tested from blood extraction and serum isolation in 33 patients diagnosed with FM and 30 healthy controls. Western blot and HPLC techniques were performed to study the different parameters. Finally, bioinformatic analysis of machine learning was performed to predict possible associations of results. Results: CoQ10 parameter did not show evidence to be a good marker of the disease, as the values are not significantly different between control and patient groups (Student’s t-test, CI 95%). For this reason, the focus of the study changed into the ratio between mitochondrial mass and autophagy levels. The bioinformatics analysis showed a possible association between this ratio and patients’ symptomatology. Finally, the effects of coenzyme Q10 as a potential treatment for the disease were different within patients, and its efficacy may be related to the initial mitochondrial status. However, there is no statistical significance due to limitations within the sample size. Conclusion: Our study supports the hypothesis that an imbalance in mitochondrial homeostasis is involved in the FM pathogenesis. However, whether the increase in oxidative stress is the result of mitochondrial imbalance or the cause of this disease remains an open question. The measurement of this imbalance might be used as a preliminary biomarker for the diagnosis and follow-up of patients with FM, and even for the evaluation of the effects of the different antioxidants therapies.es
dc.formatapplication/pdfes
dc.format.extent11 p.es
dc.language.isoenges
dc.publisherDovepresses
dc.relation.ispartofOpen Access Rheumatology: Research and Reviews, 12, 175-185.
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectFibromyalgiaes
dc.subjectDiagnosises
dc.subjectMitochondriaes
dc.subjectChronic paines
dc.titleMitochondrial imbalance as a new approach to the study of fibromyalgiaes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Citología e Histología Normal y Patológicaes
dc.relation.publisherversionhttps://www.dovepress.com/mitochondrial-imbalance-as-a-new-approach-to-the-study-of-fibromyalgia-peer-reviewed-fulltext-article-OARRRes
dc.identifier.doi10.2147/OARRR.S257470es
dc.journaltitleOpen Access Rheumatology: Research and Reviewses
dc.publication.volumen12es
dc.publication.initialPage175es
dc.publication.endPage185es

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