Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia

Antonio Martínez-Lara,1 Ana María Moreno-Fernández,2 Maripaz Jiménez-Guerrero,1 Claudia Díaz-López,1 Manuel De-Miguel,2 David Cotán,1,3 José Antonio Sánchez-Alcázar3 1Pronacera Therapeutics...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Martínez-Lara A, Moreno-Fernández AM, Jiménez-Guerrero M, Díaz-López C, De-Miguel M, Cotán D, Sánchez-Alcázar JA
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2020
Materias:
Acceso en línea:https://doaj.org/article/7cc2bd216bfc4c9a97c04e55bf15a11c
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:7cc2bd216bfc4c9a97c04e55bf15a11c
record_format dspace
spelling oai:doaj.org-article:7cc2bd216bfc4c9a97c04e55bf15a11c2021-12-02T13:07:23ZMitochondrial Imbalance as a New Approach to the Study of Fibromyalgia1179-156Xhttps://doaj.org/article/7cc2bd216bfc4c9a97c04e55bf15a11c2020-08-01T00:00:00Zhttps://www.dovepress.com/mitochondrial-imbalance-as-a-new-approach-to-the-study-of-fibromyalgia-peer-reviewed-article-OARRRhttps://doaj.org/toc/1179-156XAntonio Martínez-Lara,1 Ana María Moreno-Fernández,2 Maripaz Jiménez-Guerrero,1 Claudia Díaz-López,1 Manuel De-Miguel,2 David Cotán,1,3 José Antonio Sánchez-Alcázar3 1Pronacera Therapeutics S.L., Seville, Spain; 2Departamento de Citología e Histología Normal y Patológica, Facultad de Medicina, Universidad de Sevilla, Seville, Spain; 3Centro Andaluz de Biología del Desarrollo (CABD-CSIC-Universidad Pablo de Olavide), Seville 41013, SpainCorrespondence: David Cotán Tel +34 615 41 26 42Email david.cotan@hotmail.comBackground: 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.Keywords: fibromyalgia, diagnosis, mitochondria, chronic painMartínez-Lara AMoreno-Fernández AMJiménez-Guerrero MDíaz-López CDe-Miguel MCotán DSánchez-Alcázar JADove Medical Pressarticlefibromyalgiadiagnosismitochondriachronic pain.Diseases of the musculoskeletal systemRC925-935ENOpen Access Rheumatology: Research and Reviews, Vol Volume 12, Pp 175-185 (2020)
institution DOAJ
collection DOAJ
language EN
topic fibromyalgia
diagnosis
mitochondria
chronic pain.
Diseases of the musculoskeletal system
RC925-935
spellingShingle fibromyalgia
diagnosis
mitochondria
chronic pain.
Diseases of the musculoskeletal system
RC925-935
Martínez-Lara A
Moreno-Fernández AM
Jiménez-Guerrero M
Díaz-López C
De-Miguel M
Cotán D
Sánchez-Alcázar JA
Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
description Antonio Martínez-Lara,1 Ana María Moreno-Fernández,2 Maripaz Jiménez-Guerrero,1 Claudia Díaz-López,1 Manuel De-Miguel,2 David Cotán,1,3 José Antonio Sánchez-Alcázar3 1Pronacera Therapeutics S.L., Seville, Spain; 2Departamento de Citología e Histología Normal y Patológica, Facultad de Medicina, Universidad de Sevilla, Seville, Spain; 3Centro Andaluz de Biología del Desarrollo (CABD-CSIC-Universidad Pablo de Olavide), Seville 41013, SpainCorrespondence: David Cotán Tel +34 615 41 26 42Email david.cotan@hotmail.comBackground: 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.Keywords: fibromyalgia, diagnosis, mitochondria, chronic pain
format article
author Martínez-Lara A
Moreno-Fernández AM
Jiménez-Guerrero M
Díaz-López C
De-Miguel M
Cotán D
Sánchez-Alcázar JA
author_facet Martínez-Lara A
Moreno-Fernández AM
Jiménez-Guerrero M
Díaz-López C
De-Miguel M
Cotán D
Sánchez-Alcázar JA
author_sort Martínez-Lara A
title Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_short Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_full Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_fullStr Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_full_unstemmed Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_sort mitochondrial imbalance as a new approach to the study of fibromyalgia
publisher Dove Medical Press
publishDate 2020
url https://doaj.org/article/7cc2bd216bfc4c9a97c04e55bf15a11c
work_keys_str_mv AT martinezlaraa mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT morenofernandezam mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT jimenezguerrerom mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT diazlopezc mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT demiguelm mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT cotand mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
AT sanchezalcazarja mitochondrialimbalanceasanewapproachtothestudyoffibromyalgia
_version_ 1718393456657694720