Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

Autor: Patrick Edery, Dominique Chretien, Vanna Geromel, Pierre Rustin, Noman Kadhom, Arnold Munnich, Eeva-Liisa Appelkvist, Agnès Rötig, Lars Ernster, Gustav Dallner, Marc Lebideau
Rok vydání: 2000
Předmět:
Zdroj: Lancet (London, England). 356(9227)
ISSN: 0140-6736
Popis: Summary Background The respiratory-chain deficiencies are a broad group of largely untreatable diseases. Among them, coenzyme Q 10 (ubiquinone) deficiency constitutes a subclass that deserves early and accurate diagnosis. Methods We assessed respiratory-chain function in two siblings with severe encephalomyopathy and renal failure. We used high-performance liquid chromatography analyses, combined with radiolabelling experiments, to quantify cellular coenzyme Q 10 content. Clinical follow-up and detailed biochemical investigations of respiratory chain activity were carried out over the 3 years of oral quinone administration. Findings Deficiency of coenzyme Q 10 -dependent respiratory-chain activities was identified in muscle biopsy, circulating lymphocytes, and cultured skin fibroblasts. Undetectable coenzyme Q 10 and results of radiolabelling experiments in cultured fibroblasts supported the diagnosis of widespread coenzyme Q 10 deficiency. Stimulation of respiration and fibroblast enzyme activities by exogenous quinones in vitro prompted us to treat the patients with oral ubidecarenone (5 mg/kg daily), which resulted in a substantial improvement of their condition over 3 years of therapy. Interpretation Particular attention should be paid to multiple quinone-responsive respiratory-chain enzyme deficiency because this rare disorder can be successfully treated by oral ubidecarenone.
Databáze: OpenAIRE
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