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Mitochondrion ; 13(4): 337-41, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23583954

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.


Subject(s)
Ataxia/epidemiology , Metabolism, Inborn Errors/complications , Mitochondrial Diseases/complications , Mitochondrial Diseases/epidemiology , Mitochondrial Myopathies/complications , Muscle Weakness/epidemiology , Muscular Diseases/complications , Ubiquinone/deficiency , 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
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