Literature DB >> 20817454

Quantitative ultrasound using backscatter analysis in Duchenne and Becker muscular dystrophy.

Craig M Zaidman1, Anne M Connolly, Elizabeth C Malkus, Julaine M Florence, Alan Pestronk.   

Abstract

Evaluation of ultrasound images of muscle with calibrated muscle backscatter (cMB) provides reproducible quantitative measurements of muscle pathology. Increased cMB is associated with greater muscle pathology. We used cMB to evaluate the severity of muscle pathology in 55 patients with Duchenne and Becker Muscular Dystrophy (D/BMD) compared to 77 controls. cMB was also compared to measurements of strength and function. cMB in DMD and BMD increased linearly with age and was higher than in controls when groups are compared. cMB increased twice as fast with age in DMD than in BMD. In DMD, cMB was higher with reduced function and strength. Ultrasound measurement of muscle pathology using cMB is a sensitive and objective quantitative technique for determining the severity of muscle pathology in dystrophinopathies. Longitudinal studies are required to determine the sensitivity of this measure to changes in pathology over time.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20817454      PMCID: PMC2991397          DOI: 10.1016/j.nmd.2010.06.019

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  19 in total

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2.  Quantitative sonography of muscle.

Authors:  J Heckmatt; E Rodillo; M Doherty; K Willson; S Leeman
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4.  Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging.

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5.  Intrarater reliability of manual muscle test (Medical Research Council scale) grades in Duchenne's muscular dystrophy.

Authors:  J M Florence; S Pandya; W M King; J D Robison; J Baty; J P Miller; J Schierbecker; L C Signore
Journal:  Phys Ther       Date:  1992-02

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Authors:  J Jeppesen; A Green; B F Steffensen; J Rahbek
Journal:  Neuromuscul Disord       Date:  2003-12       Impact factor: 4.296

7.  Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy.

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Authors:  J Z Heckmatt; V Dubowitz; S Leeman
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Authors:  J Z Heckmatt; S Leeman; V Dubowitz
Journal:  J Pediatr       Date:  1982-11       Impact factor: 4.406

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  16 in total

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Review 6.  Neuromuscular ultrasonography: quantifying muscle and nerve measurements.

Authors:  David Mayans; Michael S Cartwright; Francis O Walker
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7.  Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy.

Authors:  Craig M Zaidman; Elizabeth C Malkus; Anne M Connolly
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8.  Quantitative ultrasound of skeletal muscle: reliable measurements of calibrated muscle backscatter from different ultrasound systems.

Authors:  Craig M Zaidman; Mark R Holland; Michael S Hughes
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9.  Minimal training is required to reliably perform quantitative ultrasound of muscle.

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10.  Cross-sectional evaluation of electrical impedance myography and quantitative ultrasound for the assessment of Duchenne muscular dystrophy in a clinical trial setting.

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