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Title: Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum.

Authors: Barca, Emanuele; Kleiner, Giulio; Tang, Guomei; Ziosi, Marcello; Tadesse, Saba; Masliah, Eliezer; Louis, Elan D; Faust, Phyllis; Kang, Un J; Torres, Jose; Cortes, Etty P; Vonsattel, Jean-Paul G; Kuo, Sheng-Han; Quinzii, Catarina M

Published In J Neuropathol Exp Neurol, (2016 07)

Abstract: In familial and sporadic multiple system atrophy (MSA) patients, deficiency of coenzyme Q10 (CoQ10) has been associated with mutations in COQ2, which encodes the second enzyme in the CoQ10 biosynthetic pathway. Cerebellar ataxia is the most common presentation of CoQ10 deficiency, suggesting that the cerebellum might be selectively vulnerable to low levels of CoQ10 To investigate whether CoQ10 deficiency represents a common feature in the brains of MSA patients independent of the presence of COQ2 mutations, we studied CoQ10 levels in postmortem brains of 12 MSA, 9 Parkinson disease (PD), 9 essential tremor (ET) patients, and 12 controls. We also assessed mitochondrial respiratory chain enzyme activities, oxidative stress, mitochondrial mass, and levels of enzymes involved in CoQ biosynthesis. Our studies revealed CoQ10 deficiency in MSA cerebellum, which was associated with impaired CoQ biosynthesis and increased oxidative stress in the absence of COQ2 mutations. The levels of CoQ10 in the cerebella of ET and PD patients were comparable or higher than in controls. These findings suggest that CoQ10 deficiency may contribute to the pathogenesis of MSA. Because no disease modifying therapies are currently available, increasing CoQ10 levels by supplementation or upregulation of its biosynthesis may represent a novel treatment strategy for MSA patients.

PubMed ID: 27235405 Exiting the NIEHS site

MeSH Terms: Aged; Aged, 80 and over; Ataxia/complications; Ataxia/metabolism*; Ataxia/pathology; Case-Control Studies; Cerebellum/metabolism*; Cerebellum/pathology; Female; Humans; Male; Middle Aged; Mitochondrial Diseases/complications; Mitochondrial Diseases/metabolism*; Mitochondrial Diseases/pathology; Multiple System Atrophy/complications; Multiple System Atrophy/metabolism*; Multiple System Atrophy/pathology; Muscle Weakness/complications; Muscle Weakness/metabolism*; Muscle Weakness/pathology; Oxidative Stress/physiology; Ubiquinone/analogs & derivatives*; Ubiquinone/deficiency*; Ubiquinone/metabolism

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