Volume 45, Issue 5 pp. 642-647
Research Article

Electrical impedance myography in spinal muscular atrophy: A longitudinal study

Seward B. Rutkove MD

Corresponding Author

Seward B. Rutkove MD

Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215, USA

Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215, USASearch for more papers by this author
Matt C. Gregas PhD

Matt C. Gregas PhD

Clinical Research Program, Children's Hospital Boston, Boston, Massachusetts, USA

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Basil T. Darras MD

Basil T. Darras MD

Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts, USA

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First published: 18 November 2011
Citations: 56

Abstract

Introduction: New approaches for assessing disease progression in spinal muscular atrophy (SMA) are needed. In this study, we evaluate whether electrical impedance myography (EIM) can detect disease progression in SMA compared with a group of healthy children of similar age. Methods: Twenty-eight children with SMA and 20 normal children underwent repeated EIM testing in four muscles at regular intervals for up to 3 years. An average rate of change of EIM was calculated for each subject and normalized to subcutaneous fat thickness and muscle girth. Results: Multiple EIM parameters showed a change in normal subjects over a mean of 16.7 months; however, no change was found in SMA patients over this period. Conclusions: EIM could detect non–mass-dependent muscle maturation in healthy children. In contrast, the muscle in children with SMA, as measured by EIM, was virtually static, showing no evidence of growth or active deterioration. Muscle Nerve, 2012

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