Literature DB >> 30637285

ADCK3-related Coenzyme Q10 Deficiency: A Potentially Treatable Genetic Disease.

Anna Chang1,2, Marta Ruiz-Lopez1, Elizabeth Slow1, Mark Tarnopolsky3, Anthony E Lang1, Renato P Munhoz1.   

Abstract

BACKGROUND: Disorders related to dysfunction of coenzyme (CoQ10) metabolism, including AarF domain containing kinase 3 gene (ADCK3) mutations, have received attention due to the potential for response to CoQ10 supplementation.
METHODS: We describe two new cases of neurological syndromes due to ADCK3 mutations that obtained striking benefit from CoQ10, and a third who did not. We also review 20 cases from the literature in which responses to CoQ10 were documented out of all 38 previously reported cases.
RESULTS: Despite the remarkable responses in some cases with ataxia and movement disorders (myoclonus, dystonia, tremor), overall, we were not able to identify variables that predicted response to CoQ10 supplementation.
CONCLUSIONS: Based on our experience and data from the literature, we recommend a minimum of 10 mg/kg/day of ubiquinone with titration up to 15 mg/kg/day, maintained at least for 6 months in order to obtain or exclude potential benefit from therapy.

Entities:  

Keywords:  autosomal recessive cerebellar ataxia; coenzyme Q10 deficiency; kinase 3 gene mutation

Year:  2018        PMID: 30637285      PMCID: PMC6277365          DOI: 10.1002/mdc3.12667

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


  10 in total

1.  ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?

Authors:  O Hikmat; C Tzoulis; P M Knappskog; S Johansson; H Boman; P Sztromwasser; E Lien; E Brodtkorb; D Ghezzi; L A Bindoff
Journal:  Eur J Neurol       Date:  2016-04-23       Impact factor: 6.089

2.  Coenzyme Q(10)-responsive ataxia: 2-year-treatment follow-up.

Authors:  Merce Pineda; Raquel Montero; Asuncion Aracil; Mar M O'Callaghan; Ana Mas; Carmen Espinos; Dolores Martinez-Rubio; Francesc Palau; Placido Navas; Paz Briones; Rafael Artuch
Journal:  Mov Disord       Date:  2010-07-15       Impact factor: 10.338

3.  Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3.

Authors:  Rita Horvath; Birgit Czermin; Sweena Gulati; Stephanie Demuth; Gunnar Houge; Angela Pyle; Christine Dineiger; Emma L Blakely; Adam Hassani; Charlotte Foley; Michael Brodhun; Karin Storm; Janbernd Kirschner; Grainne S Gorman; Hanns Lochmüller; Elke Holinski-Feder; Robert W Taylor; Patrick F Chinnery
Journal:  J Neurol Neurosurg Psychiatry       Date:  2011-10-29       Impact factor: 10.154

4.  Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability.

Authors:  Lubov Blumkin; Esther Leshinsky-Silver; Ayelet Zerem; Keren Yosovich; Tally Lerman-Sagie; Dorit Lev
Journal:  JIMD Rep       Date:  2013-09-19

Review 5.  Primary and secondary coenzyme Q10 deficiency: the role of therapeutic supplementation.

Authors:  Marnie Potgieter; Etheresia Pretorius; Michael S Pepper
Journal:  Nutr Rev       Date:  2013-01-30       Impact factor: 7.110

6.  CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures.

Authors:  Julie Mollet; Agnès Delahodde; Valérie Serre; Dominique Chretien; Dimitri Schlemmer; Anne Lombes; Nathalie Boddaert; Isabelle Desguerre; Pascale de Lonlay; Hélène Ogier de Baulny; Arnold Munnich; Agnès Rötig
Journal:  Am J Hum Genet       Date:  2008-03       Impact factor: 11.025

7.  Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3.

Authors:  E Barca; O Musumeci; F Montagnese; S Marino; F Granata; D Nunnari; L Peverelli; S DiMauro; C M Quinzii; A Toscano
Journal:  Clin Genet       Date:  2016-02-16       Impact factor: 4.438

8.  The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children.

Authors:  Alessandra Terracciano; Florence Renaldo; Ginevra Zanni; Adele D'Amico; Anna Pastore; Sabina Barresi; Enza Maria Valente; Fiorella Piemonte; Giulia Tozzi; Rosalba Carrozzo; Massimiliano Valeriani; Renata Boldrini; Eugenio Mercuri; Filippo Maria Santorelli; Enrico Bertini
Journal:  Eur J Paediatr Neurol       Date:  2011-08-27       Impact factor: 3.140

9.  Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation.

Authors:  Yo-Tsen Liu; Joshua Hersheson; Vincent Plagnol; Katherine Fawcett; Kate E C Duberley; Elisavet Preza; Iain P Hargreaves; Annapurna Chalasani; Matilde Laurá; Nick W Wood; Mary M Reilly; Henry Houlden
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-11-11       Impact factor: 10.154

10.  Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression.

Authors:  Cyril Mignot; Emmanuelle Apartis; Alexandra Durr; Charles Marques Lourenço; Perrine Charles; David Devos; Caroline Moreau; Pascale de Lonlay; Nathalie Drouot; Lydie Burglen; Nadine Kempf; Elsa Nourisson; Sandra Chantot-Bastaraud; Anne-Sophie Lebre; Marlène Rio; Yves Chaix; Eric Bieth; Emmanuel Roze; Isabelle Bonnet; Sandrine Canaple; Coralie Rastel; Alexis Brice; Agnès Rötig; Isabelle Desguerre; Christine Tranchant; Michel Koenig; Mathieu Anheim
Journal:  Orphanet J Rare Dis       Date:  2013-10-28       Impact factor: 4.123

  10 in total
  10 in total

1.  A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options.

Authors:  Ying Wang; Evren Gumus; Siegfried Hekimi
Journal:  Mol Genet Metab Rep       Date:  2022-05-05

2.  COQ2 mutation associated isolated nephropathy in two siblings from a Chinese pedigree.

Authors:  Min Li; Zhihui Yue; Hongrong Lin; Haiyan Wang; Huamu Chen; Liangzhong Sun
Journal:  Ren Fail       Date:  2021-12       Impact factor: 2.606

3.  Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.

Authors:  Hao-Ling Cheng; Ya-Ru Shao; Yi Dong; Hai-Lin Dong; Lu Yang; Yin Ma; Ying Shen; Zhi-Ying Wu
Journal:  Transl Neurodegener       Date:  2021-10-18       Impact factor: 8.014

Review 4.  Treatable Hyperkinetic Movement Disorders Not to Be Missed.

Authors:  Aurélie Méneret; Béatrice Garcin; Solène Frismand; Annie Lannuzel; Louise-Laure Mariani; Emmanuel Roze
Journal:  Front Neurol       Date:  2021-12-01       Impact factor: 4.003

Review 5.  Movement Disorders in Genetic Pediatric Ataxias.

Authors:  Simone Gana; Enza Maria Valente
Journal:  Mov Disord Clin Pract       Date:  2020-04-06

6.  One-year outcome of coenzyme Q10 supplementation in ADCK3 ataxia (ARCA2).

Authors:  Tommaso Schirinzi; Martina Favetta; Alberto Romano; Andrea Sancesario; Susanna Summa; Silvia Minosse; Ginevra Zanni; Enrico Castelli; Enrico Bertini; Maurizio Petrarca; Gessica Vasco
Journal:  Cerebellum Ataxias       Date:  2019-12-16

Review 7.  Disorders of Human Coenzyme Q10 Metabolism: An Overview.

Authors:  Iain Hargreaves; Robert A Heaton; David Mantle
Journal:  Int J Mol Sci       Date:  2020-09-13       Impact factor: 5.923

8.  Primary coenzyme Q10 deficiency due to COQ8A gene mutations.

Authors:  Linwei Zhang; Tetsuo Ashizawa; Dantao Peng
Journal:  Mol Genet Genomic Med       Date:  2020-08-02       Impact factor: 2.183

9.  Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy.

Authors:  Mahmoud Reza Ashrafi; Roya Haghighi; Reza Shervin Badv; Homa Ghabeli; Ali Reza Tavasoli; Elham Pourbakhtyaran; Zahra Rezaei; Nejat Mahdieh; Pouria Mohammadi; Morteza Heidari
Journal:  J Mol Neurosci       Date:  2022-03-11       Impact factor: 2.866

10.  Clinico-Genetic, Imaging and Molecular Delineation of COQ8A-Ataxia: A Multicenter Study of 59 Patients.

Authors:  Andreas Traschütz; Tommaso Schirinzi; Lucia Laugwitz; Nathan H Murray; Craig A Bingman; Selina Reich; Jan Kern; Anna Heinzmann; Gessica Vasco; Enrico Bertini; Ginevra Zanni; Alexandra Durr; Stefania Magri; Franco Taroni; Alessandro Malandrini; Jonathan Baets; Peter de Jonghe; Willem de Ridder; Matthieu Bereau; Stephanie Demuth; Christos Ganos; A Nazli Basak; Hasmet Hanagasi; Semra Hiz Kurul; Benjamin Bender; Ludger Schöls; Ute Grasshoff; Thomas Klopstock; Rita Horvath; Bart van de Warrenburg; Lydie Burglen; Christelle Rougeot; Claire Ewenczyk; Michel Koenig; Filippo M Santorelli; Mathieu Anheim; Renato P Munhoz; Tobias Haack; Felix Distelmaier; David J Pagliarini; Hélène Puccio; Matthis Synofzik
Journal:  Ann Neurol       Date:  2020-06-10       Impact factor: 11.274

  10 in total

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