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Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia

BACKGROUND: 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 po...

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Autores principales: Martínez-Lara, Antonio, Moreno-Fernández, Ana María, Jiménez-Guerrero, Maripaz, Díaz-López, Claudia, De-Miguel, Manuel, Cotán, David, Sánchez-Alcázar, José Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455536/
https://www.ncbi.nlm.nih.gov/pubmed/32922097
http://dx.doi.org/10.2147/OARRR.S257470
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author Martínez-Lara, Antonio
Moreno-Fernández, Ana María
Jiménez-Guerrero, Maripaz
Díaz-López, Claudia
De-Miguel, Manuel
Cotán, David
Sánchez-Alcázar, José Antonio
author_facet Martínez-Lara, Antonio
Moreno-Fernández, Ana María
Jiménez-Guerrero, Maripaz
Díaz-López, Claudia
De-Miguel, Manuel
Cotán, David
Sánchez-Alcázar, José Antonio
author_sort Martínez-Lara, Antonio
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-74555362020-09-11 Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia Martínez-Lara, Antonio Moreno-Fernández, Ana María Jiménez-Guerrero, Maripaz Díaz-López, Claudia De-Miguel, Manuel Cotán, David Sánchez-Alcázar, José Antonio Open Access Rheumatol Original Research BACKGROUND: 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. Dove 2020-08-24 /pmc/articles/PMC7455536/ /pubmed/32922097 http://dx.doi.org/10.2147/OARRR.S257470 Text en © 2020 Martínez-Lara et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Martínez-Lara, Antonio
Moreno-Fernández, Ana María
Jiménez-Guerrero, Maripaz
Díaz-López, Claudia
De-Miguel, Manuel
Cotán, David
Sánchez-Alcázar, José Antonio
Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title 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_short Mitochondrial Imbalance as a New Approach to the Study of Fibromyalgia
title_sort mitochondrial imbalance as a new approach to the study of fibromyalgia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455536/
https://www.ncbi.nlm.nih.gov/pubmed/32922097
http://dx.doi.org/10.2147/OARRR.S257470
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