Skip to main content
Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1987 Jun;50(6):743–746. doi: 10.1136/jnnp.50.6.743

Chronic fatigue and myalgia syndrome: mitochondrial and glycolytic studies in skeletal muscle.

E Byrne, I Trounce
PMCID: PMC1032081  PMID: 3039060

Abstract

Clinical and biochemical findings in skeletal muscle in 11 patients with chronic fatigue myalgia syndromes of unknown aetiology are reported. All patients had severe asthenia for from one to 10 years with greatly limited exercise capacity and protracted exhaustion after minor exercise. Diffuse myalgia was prominent and was exacerbated for hours to days after exercise. Assay of skeletal muscle carnitine, phosphorylase, all glycolytic enzymes and the mitochondrial marker enzymes monoamine oxidase, isocitrate dehydrogenase and cytochrome oxidase were normal. These findings lend no support to the presence of a major defect in muscle intermediary energy pathways in this syndrome.

Full text

PDF
745

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnold D. L., Bore P. J., Radda G. K., Styles P., Taylor D. J. Excessive intracellular acidosis of skeletal muscle on exercise in a patient with a post-viral exhaustion/fatigue syndrome. A 31P nuclear magnetic resonance study. Lancet. 1984 Jun 23;1(8391):1367–1369. doi: 10.1016/s0140-6736(84)91871-3. [DOI] [PubMed] [Google Scholar]
  2. Behan P. O., Behan W. M., Bell E. J. The postviral fatigue syndrome--an analysis of the findings in 50 cases. J Infect. 1985 May;10(3):211–222. doi: 10.1016/s0163-4453(85)92488-0. [DOI] [PubMed] [Google Scholar]
  3. Byrne E., Blumbergs P. C., Hallpike J. F., Mukherjee T. M. Clinical features of mitochondrial myopathy. Aust N Z J Med. 1983 Aug;13(4):353–358. doi: 10.1111/j.1445-5994.1983.tb04480.x. [DOI] [PubMed] [Google Scholar]
  4. Byrne E., Dennett X., Trounce I., Henderson R. Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia. Histochemical and biochemical studies. J Neurol Sci. 1985 Dec;71(2-3):257–271. doi: 10.1016/0022-510x(85)90064-4. [DOI] [PubMed] [Google Scholar]
  5. Byrne E. Historical and current concepts in mitochondrial myopathies. Aust N Z J Med. 1983 Jun;13(3):299–305. doi: 10.1111/j.1445-5994.1983.tb04671.x. [DOI] [PubMed] [Google Scholar]
  6. Doery J. C., Hirsh J., De Gruchy G. C. Platelet glycolytic enzymes: effect of cellular disruption procedures on activity. Br J Haematol. 1970 Aug;19(2):145–157. doi: 10.1111/j.1365-2141.1970.tb01613.x. [DOI] [PubMed] [Google Scholar]
  7. Epidemic malaise. Br Med J. 1970 Jan 3;1(5687):1–2. [PMC free article] [PubMed] [Google Scholar]
  8. HENDERSON D. A., SHELOKOV A. Epidemic neuromyasthenia; clinical syndrome. N Engl J Med. 1959 Apr 9;260(15):757–contd. doi: 10.1056/NEJM195904092601506. [DOI] [PubMed] [Google Scholar]
  9. Kanno T., Sudo K., Takeuchi I., Kanda S., Honda N., Nishimura Y., Oyama K. Hereditary deficiency of lactate dehydrogenase M-subunit. Clin Chim Acta. 1980 Dec 8;108(2):267–276. doi: 10.1016/0009-8981(80)90013-3. [DOI] [PubMed] [Google Scholar]
  10. Layzer R. B., Rowland L. P., Ranney H. M. Muscle phosphofructokinase deficiency. Arch Neurol. 1967 Nov;17(5):512–523. doi: 10.1001/archneur.1967.00470290066009. [DOI] [PubMed] [Google Scholar]
  11. Rowland L. P., Lovelace R. E., Schotland D. L., Araki S., Carmel P. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase. Neurology. 1966 Jan;16(1):93–100. doi: 10.1212/wnl.16.1.93. [DOI] [PubMed] [Google Scholar]
  12. WOLFSON S. K., Jr, WILLIAMS-ASHMAN H. G. Isocitric and 6-phosphogluconic dehydrogenases in human blood serum. Proc Soc Exp Biol Med. 1957 Oct;96(1):231–234. doi: 10.3181/00379727-96-23439. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Neurology, Neurosurgery, and Psychiatry are provided here courtesy of BMJ Publishing Group

RESOURCES