Literature DB >> 23361264

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

Douglas S Kerr1.   

Abstract

Over the last 15 years, some 16 open and controlled clinical trials for potential treatments of mitochondrial diseases have been reported or are in progress, and are summarized and reviewed herein. These include trials of administering dichloroacetate (an activator of pyruvate dehydrogenase complex), arginine or citrulline (precursors of nitric oxide), coenzyme Q10 (CoQ10; part of the electron transport chain and an antioxidant), idebenone (a synthetic analogue of CoQ10), EPI-743 (a novel oral potent 2-electron redox cycling agent), creatine (a precursor of phosphocreatine), combined administration (of creatine, α-lipoate, and CoQ10), and exercise training (to increase muscle mitochondria). These trials have included patients with various mitochondrial disorders, a selected subcategory of mitochondrial disorders, or specific mitochondrial disorders (Leber hereditary optic neuropathy or mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes). The trial designs have varied from open-label/uncontrolled, open-label/controlled, or double-blind/placebo-controlled/crossover. Primary outcomes have ranged from single, clinically-relevant scores to multiple measures. Eight of these trials have been well-controlled, completed trials. Of these only 1 (treatment with creatine) showed a significant change in primary outcomes, but this was not reproduced in 2 subsequent trials with creatine with different patients. One trial (idebenone treatment of Leber hereditary optic neuropathy) did not show significant improvement in the primary outcome, but there was significant improvement in a subgroup of patients. Despite the paucity of benefits found so far, well-controlled clinical trials are essential building blocks in the continuing search for more effective treatment of mitochondrial disease, and current trials based on information gained from these prior experiences are in progress. Because of difficulties in recruiting sufficient mitochondrial disease patients and the relatively large expense of conducting such trials, advantageous strategies include crossover designs (where possible), multicenter collaboration, and the selection of very few, clinically relevant, primary outcomes.

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Year:  2013        PMID: 23361264      PMCID: PMC3625388          DOI: 10.1007/s13311-013-0176-7

Source DB:  PubMed          Journal:  Neurotherapeutics        ISSN: 1878-7479            Impact factor:   7.620


  46 in total

1.  MELAS and L-arginine therapy.

Authors:  Yasutoshi Koga; Yukihiro Akita; Junko Nishioka; Shuichi Yatsuga; Nataliya Povalko; Koujyu Katayama; Toyojiro Matsuishi
Journal:  Mitochondrion       Date:  2006-12-05       Impact factor: 4.160

Review 2.  A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases.

Authors:  Salvatore Dimauro; Pierre Rustin
Journal:  Biochim Biophys Acta       Date:  2008-11-05

Review 3.  Leigh and Leigh-like syndrome in children and adults.

Authors:  Josef Finsterer
Journal:  Pediatr Neurol       Date:  2008-10       Impact factor: 3.372

Review 4.  Idebenone: an emerging therapy for Friedreich ataxia.

Authors:  Thomas Meier; Gunnar Buyse
Journal:  J Neurol       Date:  2009-03       Impact factor: 4.849

5.  Human CoQ10 deficiencies.

Authors:  C M Quinzii; L C López; A Naini; S DiMauro; M Hirano
Journal:  Biofactors       Date:  2008       Impact factor: 6.113

Review 6.  Treatment of mitochondrial electron transport chain disorders: a review of clinical trials over the past decade.

Authors:  Douglas S Kerr
Journal:  Mol Genet Metab       Date:  2009-11-26       Impact factor: 4.797

Review 7.  How can we treat mitochondrial encephalomyopathies? Approaches to therapy.

Authors:  Rita Horvath; Grainne Gorman; Patrick F Chinnery
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

Review 8.  New indications and controversies in arginine therapy.

Authors:  David Coman; Joy Yaplito-Lee; Avihu Boneh
Journal:  Clin Nutr       Date:  2008-07-21       Impact factor: 7.324

9.  Randomized, double-blind, placebo-controlled trial on symptomatic effects of coenzyme Q(10) in Parkinson disease.

Authors:  Alexander Storch; Wolfgang H Jost; Peter Vieregge; Jörg Spiegel; Wolfgang Greulich; Joachim Durner; Thomas Müller; Andreas Kupsch; Henning Henningsen; Wolfgang H Oertel; Gerd Fuchs; Wilfried Kuhn; Petra Niklowitz; Rainer Koch; Birgit Herting; Heinz Reichmann
Journal:  Arch Neurol       Date:  2007-05-14

10.  Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

Authors:  Julie L Murphy; Emma L Blakely; Andrew M Schaefer; Langping He; Phil Wyrick; Ronald G Haller; Robert W Taylor; Douglass M Turnbull; Tanja Taivassalo
Journal:  Brain       Date:  2008-11       Impact factor: 13.501

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  38 in total

1.  Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease.

Authors:  Min Peng; Julian Ostrovsky; Young Joon Kwon; Erzsebet Polyak; Joseph Licata; Mai Tsukikawa; Eric Marty; Jeffrey Thomas; Carolyn A Felix; Rui Xiao; Zhe Zhang; David L Gasser; Yair Argon; Marni J Falk
Journal:  Hum Mol Genet       Date:  2015-06-03       Impact factor: 6.150

2.  Regulation of substrate utilization by the mitochondrial pyruvate carrier.

Authors:  Nathaniel M Vacanti; Ajit S Divakaruni; Courtney R Green; Seth J Parker; Robert R Henry; Theodore P Ciaraldi; Anne N Murphy; Christian M Metallo
Journal:  Mol Cell       Date:  2014-10-30       Impact factor: 17.970

3.  Therapeutic strategies for Leber's hereditary optic neuropathy: A current update.

Authors:  Nuri Gueven; Dharmesh Faldu
Journal:  Intractable Rare Dis Res       Date:  2013-11

Review 4.  Otoprotectants: From Research to Clinical Application.

Authors:  Colleen G Le Prell
Journal:  Semin Hear       Date:  2019-04-26

Review 5.  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 6.  Inherited mitochondrial genomic instability and chemical exposures.

Authors:  Sherine S L Chan
Journal:  Toxicology       Date:  2017-07-26       Impact factor: 4.221

Review 7.  Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment.

Authors:  Dmitriy M Niyazov; Stephan G Kahler; Richard E Frye
Journal:  Mol Syndromol       Date:  2016-06-03

Review 8.  Emerging aspects of treatment in mitochondrial disorders.

Authors:  Shamima Rahman
Journal:  J Inherit Metab Dis       Date:  2015-05-12       Impact factor: 4.982

Review 9.  Nutritional interventions in primary mitochondrial disorders: Developing an evidence base.

Authors:  Kathryn M Camp; Danuta Krotoski; Melissa A Parisi; Katrina A Gwinn; Bruce H Cohen; Christine S Cox; Gregory M Enns; Marni J Falk; Amy C Goldstein; Rashmi Gopal-Srivastava; Gráinne S Gorman; Stephen P Hersh; Michio Hirano; Freddie Ann Hoffman; Amel Karaa; Erin L MacLeod; Robert McFarland; Charles Mohan; Andrew E Mulberg; Joanne C Odenkirchen; Sumit Parikh; Patricia J Rutherford; Shawne K Suggs-Anderson; W H Wilson Tang; Jerry Vockley; Lynne A Wolfe; Steven Yannicelli; Philip E Yeske; Paul M Coates
Journal:  Mol Genet Metab       Date:  2016-09-20       Impact factor: 4.797

Review 10.  Recent topics: the diagnosis, molecular genesis, and treatment of mitochondrial diseases.

Authors:  Kei Murayama; Masaru Shimura; Zhimei Liu; Yasushi Okazaki; Akira Ohtake
Journal:  J Hum Genet       Date:  2018-11-21       Impact factor: 3.172

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