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.
Copyright © 2013 Elsevier B.V. and Mitochondria Research Society. All rights reserved. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Ataxia / diagnosis
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Ataxia / epidemiology*
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Child
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Child, Preschool
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Chromatography, High Pressure Liquid
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DNA, Mitochondrial / analysis
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Female
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Humans
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Infant
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Infant, Newborn
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Male
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Metabolism, Inborn Errors / complications*
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Mitochondrial Diseases / complications*
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Mitochondrial Diseases / diagnosis
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Mitochondrial Diseases / epidemiology*
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Mitochondrial Myopathies / complications*
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Muscle Weakness / diagnosis
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Muscle Weakness / epidemiology*
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Muscular Diseases / complications*
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Real-Time Polymerase Chain Reaction
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Ubiquinone / analogs & derivatives
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Ubiquinone / analysis
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Ubiquinone / deficiency*
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Young Adult
Substances
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DNA, Mitochondrial
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Ubiquinone
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coenzyme Q10
Supplementary concepts
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Coenzyme Q10 Deficiency
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Deoxyguanosine Kinase Deficiency
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Mitochondrial DNA Depletion Syndrome, Myopathic Form
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Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive