Journal of Inborn Errors of Metabolism and Screening (May 2017)

Coenzyme Q in the Treatment of Mitochondrial Disease

  • Viruna Neergheen MSc,
  • Annapurna Chalasani MSc,
  • Luke Wainwright MSci, MRes,
  • Delia Yubero PhD,
  • Raquel Montero PhD,
  • Rafael Artuch MD, PhD,
  • Iain Hargreaves PhD

DOI
https://doi.org/10.1177/2326409817707771
Journal volume & issue
Vol. 5

Abstract

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Currently, there is a paucity of available treatment strategies for oxidative phosphorylation disorders. Coenzyme Q 10 (CoQ 10 ) and related synthetic quinones are the only agents to date that have proven to be beneficial in the treatment of these heterogeneous disorders. The therapeutic efficacy of CoQ 10 is not restricted to patients with an underlying CoQ 10 deficiency and is thought to result from its ability to restore electron flow in the mitochondrial respiratory chain (MRC) as well as to increase the cellular antioxidant capacity. At present, however, there is no consensus on the appropriate dosage or therapeutic plasma level of CoQ 10 , and this information will be required before CoQ 10 can be utilized effectively in the treatment of mitochondrial disease. The following review will outline our current knowledge on the use of CoQ 10 in the treatment of MRC disorders and primary CoQ 10 deficiencies.