Exercise capacity in a child with McArdle disease

J Child Neurol. 2007 Jul;22(7):880-2. doi: 10.1177/0883073807304206.

Abstract

We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and genetic evidence of McArdle disease. The patient presented with severe myalgia, proteinuria, hematuria, pyrexia, and elevated creatine kinase after swimming. After pre-exercise ingestion of sucrose, he performed treadmill exercise to symptom limitation. His peak oxygen uptake (18.8 mL/kg/min) and ventilatory threshold (16.0 mL/kg/min) were reduced by 40% and 20% compared with healthy age-matched and gender-matched controls. The results suggest that exercise capacity is reduced early in life in patients with McArdle disease and suggest the need for prophylactic exercise training (following pre-exercise feeding to prevent rhabdomyolysis) to minimize deconditioning.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Child
  • Creatine Kinase / metabolism
  • Exercise Test
  • Exercise Therapy
  • Exercise Tolerance / physiology*
  • Glycogen Storage Disease Type V / enzymology
  • Glycogen Storage Disease Type V / physiopathology*
  • Glycogen Storage Disease Type V / therapy
  • Humans
  • Male
  • Matched-Pair Analysis
  • Oxygen Consumption / physiology*
  • Reference Values

Substances

  • Creatine Kinase