• Home
  • Articles & Books
3/4/2007

Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders

By: R. Montero, R. Artuch, P. Briones, A. Nascimento, A. García-Cazorla, M.A. Vilaseca, J.A. Sánchez-Alcázar, P. Navas, J. Montoya, M. Pineda

Coenzyme Q_{10} (CoQ) deficiency syndrome is a disorder of unknown ethiology that may cause different forms of mitochondrial encephalomyopathy. In the present study our aim was to analyse CoQ concentration and mitochondrial respiratory chain (MRC) enzyme activities in muscle biopsies of patients with clinical suspicion and/or biochemical-molecular diagnosis of a mitochondrial disorder. We studied 36 patients classified into 3 groups: 1) 14 patients without a definitive diagnosis of mitochondrial disease, 2) 13 patients with decreased CI+III and II+III activities of the MRC, and 3) 9 patients with definitive diagnosis of mitochondrial disease. Only 1 of the 14 patients of group 1 showed slightly reduced CoQ values in muscle. Six of the 13 patients from group 2 showed partial CoQ deficiency in muscle and 1 of the 9 cases from group 3 presented a slight CoQ deficiency. Significantly positive correlation was observed between CI+III and CII+III activities with CoQ concentrations in the 36 muscle homogenates from patients (r=0.555; p=0.001; and r=0.460; p=0.005, respectively). In conclusion, measurement of MRC enzyme activities is a useful tool for the detection of CoQ deficiency, which should be confirmed by CoQ quantification. PMID: 16873935 [PubMed - indexed for MEDLINE]

 
Ubigenes :: Genetics of coenzyme Q deficiency in humans