Document Detail


Electromyography guides toward subgroups of mutations in muscle channelopathies.
MedLine Citation:
PMID:  15389891     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Myotonic syndromes and periodic paralyses are rare disorders of skeletal muscle characterized mainly by muscle stiffness or episodic attacks of weakness. Familial forms are caused by mutations in genes coding for skeletal muscle voltage-gated ion channels. Exercise is known to trigger, aggravate, or relieve the symptoms. Therefore, exercise can be used as a functional test in electromyography to improve the diagnosis of these muscle disorders. Abnormal changes in the compound muscle action potential can be disclosed using different exercise tests. We report the outcome of an inclusive electromyographic survey of a large population of patients with identified ion channel gene defects. Standardized protocols comprising short and long exercise tests were applied on 41 unaffected control subjects and on 51 case patients with chloride, sodium, or calcium channel mutations known to cause myotonia or periodic paralysis. These tests disclosed significant changes of compound muscle action potential, which generally matched the clinical symptoms. Combining the responses to the different tests defined five electromyographic patterns (I-V) that correlated with subgroups of mutations and may be used in clinical practice as guides for molecular diagnosis. We hypothesize that mutations are segregated into the different electromyographic patterns according to the underlying pathophysiological mechanisms.
Authors:
Emmanuel Fournier; Marianne Arzel; Damien Sternberg; Savine Vicart; Pascal Laforet; Bruno Eymard; Jean-Claude Willer; Nacira Tabti; Bertrand Fontaine
Publication Detail:
Type:  Clinical Trial; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Annals of neurology     Volume:  56     ISSN:  0364-5134     ISO Abbreviation:  Ann. Neurol.     Publication Date:  2004 Nov 
Date Detail:
Created Date:  2004-11-01     Completed Date:  2005-01-10     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7707449     Medline TA:  Ann Neurol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  650-61     Citation Subset:  IM    
Affiliation:
Department of Physiology, Groupe Hospitalier Pitié-Salpêtrière and Université Pierre et Marie Curie, Paris, France. emfou@ccr.jussieu.fr
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MeSH Terms
Descriptor/Qualifier:
Action Potentials / physiology
Adolescent
Adult
Aged
Calcium Channels / genetics,  physiology
Child
Electric Stimulation / methods
Electromyography / methods*
Exercise / physiology
Exercise Test / methods
Female
Humans
Ion Channels / classification,  genetics*
Male
Middle Aged
Muscular Diseases / classification,  genetics*,  rehabilitation
Mutation*
Potassium Channels / genetics,  physiology
Sodium Channels / genetics,  physiology
Treatment Outcome
Chemical
Reg. No./Substance:
0/Calcium Channels; 0/Ion Channels; 0/Potassium Channels; 0/Sodium Channels

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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