Muscle ultrasound measurements and functional muscle parameters in non-dystrophic myotonias suggest structural muscle changes

J. Trip*, S. Pillen, C. G. Faber, B. G. M. van Engelen, M. J. Zwarts, G. Drost

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

39 Citations (Scopus)

Abstract

Patients with non-dystrophic myotonias, including chloride (myotonia congenita) and sodium channelopathies (paramyotonia congenita/potassium aggravated myotonias), may show muscular hypertrophy in combination with some histopathological abnormalities. However, the extent of muscle changes has never been assessed objectively in a large group genetically confirmed patients. This study quantitatively determines echo intensities, thicknesses, ranges-of-motion and force of four skeletal muscles in 63 genetically confirmed patients. The main findings revealed elevated echo intensities in all Muscles except the rectus femoris (+1.3-2.2 SID, p <0.0001), and hypertrophy in the arms (+0.5-0.9 SD, p <0.01). Muscle echo intensities were inversely correlated to the corresponding ranges-of-motion (biceps brachii: r=-0.43; p <0.001, forearm flexors: r = -0.47: p <0.001, rectus femoris: r = -0.40; p = 0.001, and tibial anterior: r = -0.27; p = 0.04) and correlated positively to age (r = 0.22; p = 0.05). The echo intensity of the forearm flexors was inversely correlated to their muscles' force (r = -0.30; p = 0.02). Together, these data suggest that non-dystrophic myotonias may lead to structural muscle changes. (C) 2009 Elsevier B.V. All rights reserved.

Original languageEnglish
Pages (from-to)462-467
Number of pages6
JournalNeuromuscular disorders
Volume19
Issue number7
DOIs
Publication statusPublished - Jul-2009
Externally publishedYes

Keywords

  • Non-dystrophic myotonias
  • Chloride channelopathies
  • Sodium channelopathies
  • Muscle ultrasound
  • Structural muscle changes
  • HYPERKALEMIC PERIODIC PARALYSIS
  • SKELETAL-MUSCLE
  • PARAMYOTONIA-CONGENITA
  • NEUROMUSCULAR DISEASE
  • REFERENCE VALUES
  • CHILDREN
  • MUTATION
  • BIOPSY
  • ULTRASONOGRAPHY
  • MYOPATHIES

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