Voluntary Muscle Involvement in Hypertrophic Cardiomyopathy

A Study of Eleven Patients

  1. ELDON R. SMITH, M.D., F.R.C.P.(C);
  2. LeROY P. HEFFERNAN, M.D., F.R.CP.(C);
  3. VIRGILIO E. SANGALANG, M.D.;
  4. LYNDA M. VAUGHAN, M.SC.; and
  5. C. SUSAN FLEMINGTON, B.SC.
  1. Halifax, Nova Scotia
    , Canada

    Abstract

    Hypertrophic cardiomyopathy is generally considered to be a primary disease of cardiac muscle, although several clinical observations suggest that the pathologic process might be more diffuse. To further examine this possibility, electromyography and voluntary muscle biopsies were done on 11 patients with hypertrophic cardiomyopathy. In 10 of 10 patients electromyography showed reductions in mean potential amplitude and duration, with an increased incidence of short-duration polyphasic deflections (findings traditionally accepted as indicative of a myopathic process). Light and electron microscopic studies of the biopsy material showed abnormalities in eight of 11 patients: four had central core or target fibers, or both, and two of these, plus four others, had subsarcolemmal mitochondrial proliferation with or without abnormal ultrastructure. These findings indicate that hypertrophic cardiomyopathy is only one aspect of a larger disease spectrum, with abnormalities in both voluntary and cardiac muscle.

    Article and Author Information

    • ▸From the Departments of Medicine and Pathology, Dalhousie University and the Victoria General Hospital; Halifax, Nova Scotia, Canada.

    • Grant support: by a grant from the Nova Scotia Division of the Canadian Heart Foundations; and grants MA-5175 and MA-5145 from the Medical Research Council of Canada.

    • ▸Requests for reprints should be addressed to Eldon R. Smith, M.D.; Department of Medicine, Victoria General Hospital; Halifax, NS B3H 2Y9, Canada.

      • Received April 13, 1976.
      • Accepted July 30, 1976.
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