CINRG pilot trial of coenzyme Q10 in Steroid-Treated duchenne muscular dystrophy

  • Christopher F. Spurney
  • , Tesi Rocha Carolina
  • , Erik Henricson
  • , Julaine Florence
  • , Jill Mayhew
  • , Ksenija Gorni
  • , Livia Pasquali
  • , Alan Pestronk
  • , Gerard R. Martin
  • , Fengming Hu
  • , Lei Nie
  • , Anne M. Connolly
  • , Diana M. Escolar

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

Introduction: Corticosteroid treatment slows disease progression and is the standard of care for Duchenne muscular dystrophy (DMD). Coenzyme Q10 (CoQ10) is a potent antioxidant that may improve function in dystrophin-deficient muscle. Methods: We performed an open-label, 'add-on' pilot study of CoQ10 in thirteen 5-10-year-old DMD patients on steroids. The primary outcome measure was the total quantitative muscle testing (QMT) score. Results: Twelve of 16 children (mean age 8.03 ± 1.64 years) completed the trial. Target serum levels of CoQ10 (≥2.5 μg/ml) were shown to be subjectand administration-dependent. Nine of 12 subjects showed an increase in total QMT score. Overall, CoQ10 treatment resulted in an 8.5% increase in muscle strength (P = 0.03). Conclusions: Addition of CoQ10 to prednisone therapy in DMD patients resulted in an increase in muscle strength. These results warrant a larger, controlled trial of CoQ10 in DMD

Original languageEnglish
Pages (from-to)174-178
Number of pages5
JournalMuscle and Nerve
Volume44
Issue number2
DOIs
StatePublished - Aug 2011

Keywords

  • Clinical trial
  • CoQ10
  • Duchenne muscular dystrophy
  • Muscle strength testing
  • Steroids

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