Literature DB >> 22987687

A quantitative measure of handgrip myotonia in non-dystrophic myotonia.

Jeffrey M Statland1, Brian N Bundy, Yunxia Wang, Jaya R Trivedi, Dipa Raja Rayan, Laura Herbelin, Merideth Donlan, Rhonda McLin, Katy J Eichinger, Karen Findlater, Liz Dewar, Shree Pandya, William B Martens, Shannon L Venance, Emma Matthews, Anthony A Amato, Michael G Hanna, Robert C Griggs, Richard J Barohn.   

Abstract

INTRODUCTION: Non-dystrophic myotonia (NDM) is characterized by myotonia without muscle wasting. A standardized quantitative myotonia assessment (QMA) is important for clinical trials.
METHODS: Myotonia was assessed in 91 individuals enrolled in a natural history study using a commercially available computerized handgrip myometer and automated software. Average peak force and 90% to 5% relaxation times were compared with historical normal controls studied with identical methods.
RESULTS: Thirty subjects had chloride channel mutations, 31 had sodium channel mutations, 6 had DM2 mutations, and 24 had no identified mutation. Chloride channel mutations were associated with prolonged first handgrip relaxation times and warm-up on subsequent handgrips. Sodium channel mutations were associated with prolonged first handgrip relaxation times and paradoxical myotonia or warm-up, depending on underlying mutations. DM2 subjects had normal relaxation times but decreased peak force. Sample size estimates are provided for clinical trial planning.
CONCLUSION: QMA is an automated, non-invasive technique for evaluating myotonia in NDM.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22987687      PMCID: PMC3564214          DOI: 10.1002/mus.23402

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


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4.  Transient paresis in myotonic syndromes. A surface EMG study.

Authors:  M J Zwarts; T W van Weerden
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