The treatment of mitochondrial myopathies and encephalomyopathies

Biochim Biophys Acta. 1995 May 24;1271(1):275-80. doi: 10.1016/0925-4439(95)00039-7.

Abstract

This paper briefly summarizes the results of a long-term, open pharmacotherapy trial in 16 patients with well-characterized mitochondrial disease. Outcome measures included repeated clinical evaluation, 31P-NMR spectroscopy and near-infrared spectroscopy. Treated patients appeared to survive longer with less functional disability and medical complications than typically seen in clinical practice.

Publication types

  • Clinical Trial
  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Antioxidants / therapeutic use*
  • Ascorbic Acid / therapeutic use
  • Child
  • Coenzymes
  • Female
  • Humans
  • Kearns-Sayre Syndrome / drug therapy*
  • Kearns-Sayre Syndrome / metabolism
  • MELAS Syndrome / drug therapy*
  • MELAS Syndrome / metabolism
  • MERRF Syndrome / drug therapy*
  • MERRF Syndrome / metabolism
  • Male
  • Methylprednisolone / therapeutic use*
  • Middle Aged
  • Mitochondrial Myopathies / drug therapy*
  • Mitochondrial Myopathies / metabolism
  • Oxidative Phosphorylation
  • Oxygen Consumption
  • Treatment Outcome
  • Ubiquinone / analogs & derivatives
  • Ubiquinone / therapeutic use
  • Vitamin E / therapeutic use
  • Vitamin K / therapeutic use
  • Vitamins / therapeutic use*

Substances

  • Antioxidants
  • Coenzymes
  • Vitamins
  • Vitamin K
  • Ubiquinone
  • Vitamin E
  • coenzyme Q10
  • Ascorbic Acid
  • Methylprednisolone