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 language | English |
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Pages (from-to) | 462-467 |
Number of pages | 6 |
Journal | Neuromuscular disorders |
Volume | 19 |
Issue number | 7 |
DOIs | |
Publication status | Published - Jul-2009 |
Externally published | Yes |
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