Abstract
Introduction: Electrical impedance myography (EIM) is a non-invasive, painless, objective technique to quantify muscle pathology. Methods: We measured EIM in 8 arm and leg muscles in 61 boys with Duchenne muscular dystrophy (DMD) and 31 healthy boys, ages 3-12 years, at 5 centers. We determined the reliability of EIM and compared results in boys with DMD to controls and to 6-minute walk distance (6MWD), North Star Ambulatory Assessment (NSAA), timed functional tests (TFTs), and strength (hand-held dynamometry). Results: EIM was well tolerated and had good inter- and intrarater reliability (intraclass correlation coefficient 0.81-0.96). The averaged EIM phase value from all muscles was higher (P<0.001) in controls (10.45±2.29) than boys with DMD (7.31±2.23), and correlated (P≤0.001) with 6MWD (r=0.55), NSAA (r=0.66), TFTs (r=-0.56), and strength (r=0.44). Conclusion: EIM is a reliable and valid measure of disease severity in DMD. Longitudinal studies comparing EIM with other assessments over time in DMD are warranted.
Original language | English |
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Pages (from-to) | 592-597 |
Number of pages | 6 |
Journal | Muscle and Nerve |
Volume | 52 |
Issue number | 4 |
DOIs | |
State | Published - Oct 1 2015 |
Keywords
- Biomarker
- Children
- Duchenne muscular dystrophy
- Electrical impedance myography
- Myopathy