Literature DB >> 23022402

Design and implementation of the first randomized controlled trial of coenzyme CoQ₁₀ in children with primary mitochondrial diseases.

Peter W Stacpoole1, Ton J deGrauw, Annette S Feigenbaum, Charles Hoppel, Douglas S Kerr, Shawn E McCandless, Michael V Miles, Brian H Robinson, Peter H Tang.   

Abstract

We report the design and implementation of the first phase 3 trial of CoenzymeQ₁₀ (CoQ₁₀) in children with genetic mitochondrial diseases. A novel, rigorous set of eligibility criteria was established. The trial, which remains open to recruitment, continues to address multiple challenges to the recruitment of patients, including widely condoned empiric use of CoQ₁₀ by individuals with proven or suspected mitochondrial disease and skepticism among professional and lay mitochondrial disease communities about participating in placebo-controlled trials. These attitudes represent significant barriers to the ethical and scientific evaluation--and ultimate approval--of nutritional and pharmacological therapies for patients with life-threatening inborn errors of energy metabolism.
Copyright © 2012 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

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Year:  2012        PMID: 23022402      PMCID: PMC3975832          DOI: 10.1016/j.mito.2012.09.005

Source DB:  PubMed          Journal:  Mitochondrion        ISSN: 1567-7249            Impact factor:   4.160


  31 in total

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3.  Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.

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Journal:  Neurology       Date:  2001-04-10       Impact factor: 9.910

4.  Neonatal presentation of coenzyme Q10 deficiency.

Authors:  S Rahman; I Hargreaves; P Clayton; S Heales
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5.  Effects of coenzyme Q10 in early Parkinson disease: evidence of slowing of the functional decline.

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Review 9.  Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits.

Authors:  Vanna Geromel; Niklas Darin; Dominique Chrétien; Paule Bénit; Pascale DeLonlay; Agnès Rötig; Arnold Munnich; Pierre Rustin
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  12 in total

Review 1.  Maternally inherited mitochondrial respiratory disorders: from pathogenetic principles to therapeutic implications.

Authors:  Martine Uittenbogaard; Anne Chiaramello
Journal:  Mol Genet Metab       Date:  2020-06-27       Impact factor: 4.797

Review 2.  Drug development for rare mitochondrial disorders.

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Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 3.  Therapeutic Approaches to Treat Mitochondrial Diseases: "One-Size-Fits-All" and "Precision Medicine" Strategies.

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Review 5.  Mitochondrial dysfunction in cardiac aging.

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6.  Succinyl-CoA synthetase (SUCLA2) deficiency in two siblings with impaired activity of other mitochondrial oxidative enzymes in skeletal muscle without mitochondrial DNA depletion.

Authors:  Xiaoping Huang; Jirair K Bedoyan; Didem Demirbas; David J Harris; Alexander Miron; Simone Edelheit; George Grahame; Suzanne D DeBrosse; Lee-Jun Wong; Charles L Hoppel; Douglas S Kerr; Irina Anselm; Gerard T Berry
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7.  Risk factors for poor bone health in primary mitochondrial disease.

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Review 8.  Sleep disorders associated with primary mitochondrial diseases.

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Review 9.  Review of clinical trials for mitochondrial disorders: 1997-2012.

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Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 10.  Development of pharmacological strategies for mitochondrial disorders.

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