Literature DB >> 8582409

Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapy.

G Kurlemann1, I Paetzke, H Möller, H Masur, G Schuierer, J Weglage, H G Koch.   

Abstract

A therapeutic trial with polyvitamins and dichloroacetate (DCA) in combination with thiamine in a 13-year-old girl with complex I deficiency is reported. The polyvitamin therapy included thiamine, riboflavin, ascorbate, coenzyme Q 10 and carnitine. This therapeutic regine was used over a period of 17 months without any effect. Although DCA lowered the lactate concentration in blood and CNS--measured by magnetic resonance spectroscopy--no clinical benefit was achieved. After 20 weeks of DCA therapy a distal polyneuropathy with areflexia developed although 100 mg thiamine daily as comedication was given from the beginning of DCA therapy. Nerve conduction velocity of the peroneal nerve was not detectable, sensible evoked potentials of the tibialis posterious nerve were normal. This side-effect resolved completely within 6 months after omission of DCA. Our observation suggests a direct toxic effect of DCA only on the peripheral nervous system in our patient since several cerebral MRI and magnetic resonance spectroscopy studies showed no abnormalities. CONCLUSION. DCA lowers the lactate concentration in children with complex I deficiency of the respiratory chain in a dose of 100 mg/kg body weight without clinical benefit. Reversible peripheral polyneuropathy may develop under DCA therapy despite thiamine medication.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8582409     DOI: 10.1007/bf01957508

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  17 in total

1.  Treatment of chronic congenital lactic acidosis by oral administration of dichloroacetate.

Authors:  Y Kuroda; M Ito; K Toshima; E Takeda; E Naito; T J Hwang; T Hashimoto; M Miyao; M Masuda; K Yamashita
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

Review 2.  Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach.

Authors:  J M Trijbels; R C Sengers; W Ruitenbeek; J C Fischer; J A Bakkeren; A J Janssen
Journal:  Eur J Pediatr       Date:  1988-11       Impact factor: 3.183

Review 3.  Therapy of mitochondrial disorders.

Authors:  H Przyrembel
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

Review 4.  The pharmacology of dichloroacetate.

Authors:  P W Stacpoole
Journal:  Metabolism       Date:  1989-11       Impact factor: 8.694

5.  Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation.

Authors:  J B Clark; D J Hayes; J A Morgan-Hughes; E Byrne
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.

Authors:  T Ichiki; M Tanaka; M Nishikimi; H Suzuki; T Ozawa; M Kobayashi; Y Wada
Journal:  Ann Neurol       Date:  1988-03       Impact factor: 10.422

7.  Congenital lactic acidosis.

Authors:  Y Kuroda; E Naito; E Takeda; I Yokota; M Miyao
Journal:  Enzyme       Date:  1987

8.  Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine.

Authors:  P L Bernsen; F J Gabreëls; W Ruitenbeek; R C Sengers; A M Stadhouders; W O Renier
Journal:  Arch Neurol       Date:  1991-03

9.  Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.

Authors:  Y Koga; I Nonaka; M Kobayashi; M Tojyo; K Nihei
Journal:  Ann Neurol       Date:  1988-12       Impact factor: 10.422

Review 10.  Lactic acidosis in childhood: Part I.

Authors:  O B Evans
Journal:  Pediatr Neurol       Date:  1985 Nov-Dec       Impact factor: 3.372

View more
  7 in total

Review 1.  Treatment options for lactic acidosis and metabolic crisis in children with mitochondrial disease.

Authors:  Katharina Danhauser; Jan A M Smeitink; Peter Freisinger; Wolfgang Sperl; Hemmen Sabir; Berit Hadzik; Ertan Mayatepek; Eva Morava; Felix Distelmaier
Journal:  J Inherit Metab Dis       Date:  2015-02-17       Impact factor: 4.982

Review 2.  Targeting Myocardial Substrate Metabolism in the Failing Heart: Ready for Prime Time?

Authors:  Salva R Yurista; Shi Chen; Aidan Welsh; W H Wilson Tang; Christopher T Nguyen
Journal:  Curr Heart Fail Rep       Date:  2022-05-14

3.  Pyruvate Dehydrogenase Kinase-mediated Glycolytic Metabolic Shift in the Dorsal Root Ganglion Drives Painful Diabetic Neuropathy.

Authors:  Md Habibur Rahman; Mithilesh Kumar Jha; Jong-Heon Kim; Youngpyo Nam; Maan Gee Lee; Younghoon Go; Robert A Harris; Dong Ho Park; Hyun Kook; In-Kyu Lee; Kyoungho Suk
Journal:  J Biol Chem       Date:  2016-01-14       Impact factor: 5.157

Review 4.  Cardiac metabolism and its interactions with contraction, growth, and survival of cardiomyocytes.

Authors:  Stephen C Kolwicz; Suneet Purohit; Rong Tian
Journal:  Circ Res       Date:  2013-08-16       Impact factor: 17.367

Review 5.  Treatment for mitochondrial disorders.

Authors:  Gerald Pfeffer; Kari Majamaa; Douglass M Turnbull; David Thorburn; Patrick F Chinnery
Journal:  Cochrane Database Syst Rev       Date:  2012-04-18

6.  Metabolic Connection of Inflammatory Pain: Pivotal Role of a Pyruvate Dehydrogenase Kinase-Pyruvate Dehydrogenase-Lactic Acid Axis.

Authors:  Mithilesh Kumar Jha; Gyun Jee Song; Maan Gee Lee; Nam Ho Jeoung; Younghoon Go; Robert A Harris; Dong Ho Park; Hyun Kook; In-Kyu Lee; Kyoungho Suk
Journal:  J Neurosci       Date:  2015-10-21       Impact factor: 6.167

7.  Pharmacological activation of the pyruvate dehydrogenase complex reduces statin-mediated upregulation of FOXO gene targets and protects against statin myopathy in rodents.

Authors:  Joanne E Mallinson; Dumitru Constantin-Teodosiu; Philip D Glaves; Elizabeth A Martin; Wendy J Davies; F Russell Westwood; James E Sidaway; Paul L Greenhaff
Journal:  J Physiol       Date:  2012-10-08       Impact factor: 5.182

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.