Literature DB >> 3941783

Treatment of Kearns-Sayre syndrome with coenzyme Q10.

S Ogasahara, Y Nishikawa, S Yorifuji, F Soga, Y Nakamura, M Takahashi, S Hashimoto, N Kono, S Tarui.   

Abstract

We studied the metabolism of coenzyme Q10 (CoQ) and the effects of CoQ therapy in five patients with Kearns-Sayre syndrome (KSS). Although the mitochondrial fraction was increased in muscles from KSS patients, CoQ content was slightly low. CoQ synthesis was normal in fibroblasts from KSS patients. Administration of 120 to 150 mg/d of CoQ improved abnormal metabolism of pyruvate and NADH oxidation in skeletal muscle. CoQ therapy decreased CSF protein concentration and CSF lactate/pyruvate ratio. ECG abnormalities and neurologic symptoms also improved.

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Year:  1986        PMID: 3941783     DOI: 10.1212/wnl.36.1.45

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  24 in total

1.  Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.

Authors:  H R Scholte; H F Busch; I E Luyt-Houwen; M H Vaandrager-Verduin; H Przyrembel; W F Arts
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study.

Authors:  C Doriguzzi; L Palmucci; B Pollo; T Mongini; M Maniscalco; L Chiadò-Piat; D Schiffer
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

3.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.

Authors:  M Yamamoto; T Sato; M Anno; H Ujike; M Takemoto
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-11       Impact factor: 10.154

4.  Adult-onset mitochondrial myopathy.

Authors:  J Fernandez-Sola; J Casademont; J M Grau; F Graus; F Cardellach; E Pedrol; A Urbano-Marquez
Journal:  Postgrad Med J       Date:  1992-03       Impact factor: 2.401

Review 5.  Therapeutic Approaches to Treat Mitochondrial Diseases: "One-Size-Fits-All" and "Precision Medicine" Strategies.

Authors:  Emanuela Bottani; Costanza Lamperti; Alessandro Prigione; Valeria Tiranti; Nicola Persico; Dario Brunetti
Journal:  Pharmaceutics       Date:  2020-11-11       Impact factor: 6.321

Review 6.  Mitochondrial encephalomyopathies: what next?

Authors:  S DiMauro
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

7.  Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Authors:  J M Shoffner; M T Lott; A S Voljavec; S A Soueidan; D A Costigan; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

8.  Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus.

Authors:  S Zierz; G Jahns; F Jerusalem
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

9.  De Toni-Debré-Fanconi syndrome in a patient with Kearns-Sayre syndrome: a case report.

Authors:  Cristina Maria Mihai; Doina Catrinoiu; Marius Toringhibel; Ramona Mihaela Stoicescu; Anca Hancu
Journal:  J Med Case Rep       Date:  2009-11-03

10.  Alzheimer's disease: A hypothesis on pathogenesis.

Authors:  D Harman
Journal:  J Am Aging Assoc       Date:  2000-07
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