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Electrical impedance myography in Duchenne muscular dystrophy and healthy controls: A multicenter study of reliability and validity.
Zaidman, Craig M; Wang, Lucy L; Connolly, Anne M; Florence, Julaine; Wong, Brenda L; Parsons, Julie A; Apkon, Susan; Goyal, Namita; Williams, Eugene; Escolar, Diana; Rutkove, Seward B; Bohorquez, Jose L.
  • Zaidman CM; Department of Neurology, Washington University School of Medicine, 660 South Euclid Avenue, Box 8111, St. Louis, Missouri, 63110, USA.
  • Wang LL; Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Connolly AM; Skulpt, Inc, Boston, Massachusetts, USA.
  • Florence J; Department of Neurology, Washington University School of Medicine, 660 South Euclid Avenue, Box 8111, St. Louis, Missouri, 63110, USA.
  • Wong BL; Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Parsons JA; Department of Neurology, Washington University School of Medicine, 660 South Euclid Avenue, Box 8111, St. Louis, Missouri, 63110, USA.
  • Apkon S; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Goyal N; Department of Pediatrics and Neurology, University of Colorado, Denver, Colorado, USA.
  • Williams E; Department of Rehabilitation Medicine, University of Washington, Seattle, Washington, USA.
  • Escolar D; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rutkove SB; DART Therapeutics, Inc, Stockbridge, Massachusetts, USA.
  • Bohorquez JL; DART Therapeutics, Inc, Stockbridge, Massachusetts, USA.
Muscle Nerve ; 52(4): 592-7, 2015 Oct.
Article en En | MEDLINE | ID: mdl-25702806
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Impedancia Eléctrica / Músculo Esquelético / Distrofia Muscular de Duchenne / Fuerza Muscular Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Impedancia Eléctrica / Músculo Esquelético / Distrofia Muscular de Duchenne / Fuerza Muscular Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article