Diagnosis of muscular glycogenosis by in vivo natural abundance 13C NMR spectroscopy

Neuromuscul Disord. 1991;1(2):99-101. doi: 10.1016/0960-8966(91)90056-x.

Abstract

Natural abundance 13C NMR (nuclear magnetic resonance) spectroscopy was used to distinguish patients suffering from muscle glycogenosis type V (McArdle's disease) from normal subjects by measuring their muscle glycogen content at rest. Proton-decoupled 13C spectra were obtained in 10-15 min from calf muscles at rest. The ratio of the glycogen/creatine signal areas was 12.9 +/- 1.7 in four McArdle's disease patients and 2.0 +/- 0.7 in seven normal subjects. This technique thus allows the non-invasive diagnosis of muscle glycogenosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Creatine / chemistry
  • Glycogen / chemistry
  • Glycogen Storage Disease Type V / diagnosis*
  • Humans
  • Magnetic Resonance Spectroscopy
  • Middle Aged
  • Muscles / chemistry

Substances

  • Glycogen
  • Creatine