ELECTRICAL IMPEDANCE MYOGRAPHY DISCRIMINATES CONGENITAL MUSCULAR DYSTROPHY FROM CONTROLS

被引:10
|
作者
Schwartz, Daniel P. [1 ]
Dastgir, Jahannaz [2 ,3 ]
Salman, Anam [1 ]
Lear, Barbara [1 ]
Boennemann, Carsten G. [2 ]
Lehky, Tanya J. [1 ]
机构
[1] NINDS, Electromyog Sect, NIH, Bldg 10,CRC Room 7SW-5680,10 Ctr Dr MSC 1404, Bethesda, MD 20892 USA
[2] NINDS, Neuromuscular & Neurogenet Disorders Childhood Se, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[3] Columbia Univ, Med Ctr, Dept Neurol, Div Pediat Neurol Neuromuscular Med, New York, NY USA
关键词
congenital muscular dystrophy; electrical impedance myography; handheld array; pediatric; subcutaneous fat; HELD ELECTRODE ARRAY; DISEASE; ATROPHY;
D O I
10.1002/mus.24770
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Electrical impedance myography (EIM) is an emerging non-invasive, highly reproducible electrophysiological technique that objectively characterizes muscle structure and composition by measuring bioimpedance. We assessed the ability of EIM ability to discriminate 2 forms of congenital muscular dystrophy (CMD), laminin alpha 2 (LAMA2)-deficient CMD and collagen VI-deficient (COL6) CMD, from a group of healthy children. We also investigated correlations between subcutaneous fat thickness and EIM parameters. Methods: Twenty-eight children with LAMA2 CMD (n=12) or COL6 (n=16) CMD and 18 normal children underwent EIM testing. Results: The EIM 50-kHZ phase was decreased in LAMA2 and COL6 CMD when compared with controls (P<0.001). Reactance, however, was decreased in COL6 but not LAMA2 CMD compared with controls (P<0.001). Conclusions: Our findings suggest that EIM may be useful in discriminating CMD from controls and may serve as a useful biomarker to follow disease progression in clinical trials.
引用
收藏
页码:402 / 406
页数:5
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