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The Value of Coenzyme Q(10) Determination in Mitochondrial Patients

Coenzyme Q(10) (CoQ) is a lipid that is ubiquitously synthesized in tissues and has a key role in mitochondrial oxidative phosphorylation. Its biochemical determination provides insight into the CoQ status of tissues and may detect CoQ deficiency that can result from either an inherited primary defi...

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Detalles Bibliográficos
Autores principales: Yubero, Delia, Allen, George, Artuch, Rafael, Montero, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406769/
https://www.ncbi.nlm.nih.gov/pubmed/28338638
http://dx.doi.org/10.3390/jcm6040037
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author Yubero, Delia
Allen, George
Artuch, Rafael
Montero, Raquel
author_facet Yubero, Delia
Allen, George
Artuch, Rafael
Montero, Raquel
author_sort Yubero, Delia
collection PubMed
description Coenzyme Q(10) (CoQ) is a lipid that is ubiquitously synthesized in tissues and has a key role in mitochondrial oxidative phosphorylation. Its biochemical determination provides insight into the CoQ status of tissues and may detect CoQ deficiency that can result from either an inherited primary deficiency of CoQ metabolism or may be secondary to different genetic and environmental conditions. Rapid identification of CoQ deficiency can also allow potentially beneficial treatment to be initiated as early as possible. CoQ may be measured in different specimens, including plasma, blood mononuclear cells, platelets, urine, muscle, and cultured skin fibroblasts. Blood and urinary CoQ also have good utility for CoQ treatment monitoring.
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spelling pubmed-54067692017-04-27 The Value of Coenzyme Q(10) Determination in Mitochondrial Patients Yubero, Delia Allen, George Artuch, Rafael Montero, Raquel J Clin Med Review Coenzyme Q(10) (CoQ) is a lipid that is ubiquitously synthesized in tissues and has a key role in mitochondrial oxidative phosphorylation. Its biochemical determination provides insight into the CoQ status of tissues and may detect CoQ deficiency that can result from either an inherited primary deficiency of CoQ metabolism or may be secondary to different genetic and environmental conditions. Rapid identification of CoQ deficiency can also allow potentially beneficial treatment to be initiated as early as possible. CoQ may be measured in different specimens, including plasma, blood mononuclear cells, platelets, urine, muscle, and cultured skin fibroblasts. Blood and urinary CoQ also have good utility for CoQ treatment monitoring. MDPI 2017-03-24 /pmc/articles/PMC5406769/ /pubmed/28338638 http://dx.doi.org/10.3390/jcm6040037 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yubero, Delia
Allen, George
Artuch, Rafael
Montero, Raquel
The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title_full The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title_fullStr The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title_full_unstemmed The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title_short The Value of Coenzyme Q(10) Determination in Mitochondrial Patients
title_sort value of coenzyme q(10) determination in mitochondrial patients
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406769/
https://www.ncbi.nlm.nih.gov/pubmed/28338638
http://dx.doi.org/10.3390/jcm6040037
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