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Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes.
- Source :
-
Mitochondrion [Mitochondrion] 2013 Jul; Vol. 13 (4), pp. 337-41. Date of Electronic Publication: 2013 Apr 11. - Publication Year :
- 2013
-
Abstract
- We evaluated coenzyme Q₁₀ (CoQ) levels in patients studied under suspicion of mitochondrial DNA depletion syndromes (MDS) (n=39). CoQ levels were quantified by HPLC, and the percentage of mtDNA depletion by quantitative real-time PCR. A high percentage of MDS patients presented with CoQ deficiency as compared to other mitochondrial patients (Mann-Whitney-U test: p=0.001). Our findings suggest that MDS are frequently associated with CoQ deficiency, as a possible secondary consequence of disease pathophysiology. Assessment of muscle CoQ status seems advisable in MDS patients since the possibility of CoQ supplementation may then be considered as a candidate therapy.<br /> (Copyright © 2013 Elsevier B.V. and Mitochondria Research Society. All rights reserved. All rights reserved.)
- Subjects :
- Adolescent
Ataxia diagnosis
Child
Child, Preschool
Chromatography, High Pressure Liquid
DNA, Mitochondrial analysis
Female
Humans
Infant
Infant, Newborn
Male
Mitochondrial Diseases diagnosis
Muscle Weakness diagnosis
Real-Time Polymerase Chain Reaction
Ubiquinone analogs & derivatives
Ubiquinone analysis
Young Adult
Ataxia epidemiology
Metabolism, Inborn Errors complications
Mitochondrial Diseases complications
Mitochondrial Diseases epidemiology
Mitochondrial Myopathies complications
Muscle Weakness epidemiology
Muscular Diseases complications
Ubiquinone deficiency
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8278
- Volume :
- 13
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Mitochondrion
- Publication Type :
- Academic Journal
- Accession number :
- 23583954
- Full Text :
- https://doi.org/10.1016/j.mito.2013.04.001