Literature DB >> 32737968

Magnetic Resonance Imaging Studies in Duchenne Muscular Dystrophy: Linking Findings to the Physical Therapy Clinic.

Claudia R Senesac1, Alison M Barnard2, Donovan J Lott3, Kavya S Nair3, Ann T Harrington4, Rebecca J Willcocks3, Kirsten L Zilke5, William D Rooney6, Glenn A Walter2, Krista Vandenborne3.   

Abstract

Duchenne muscular dystrophy (DMD) is a muscle degenerative disorder that manifests in early childhood and results in progressive muscle weakness. Physical therapists have long been an important component of the multidisciplinary team caring for people with DMD, providing expertise in areas of disease assessment, contracture management, assistive device prescription, and exercise prescription. Over the last decade, magnetic resonance imaging of muscles in people with DMD has led to an improved understanding of the muscle pathology underlying the clinical manifestations of DMD. Findings from magnetic resonance imaging (MRI) studies in DMD, paired with the clinical expertise of physical therapists, can help guide research that leads to improved physical therapist care for this unique patient population. The 2 main goals of this perspective article are to (1) summarize muscle pathology and disease progression findings from qualitative and quantitative muscle MRI studies in DMD and (2) link MRI findings of muscle pathology to the clinical manifestations observed by physical therapists with discussion of any potential implications of MRI findings on physical therapy management.
© The Author(s) 2020. Published by Oxford University Press on behalf of the American Physical Therapy Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Muscle Weakness; Muscular Dystroophies; Neuromuscular Diseases

Mesh:

Year:  2020        PMID: 32737968      PMCID: PMC7596892          DOI: 10.1093/ptj/pzaa140

Source DB:  PubMed          Journal:  Phys Ther        ISSN: 0031-9023


  80 in total

1.  A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy.

Authors:  S A Hyde; I FlŁytrup; S Glent; A K Kroksmark; B Salling; B F Steffensen; U Werlauff; M Erlandsen
Journal:  Neuromuscul Disord       Date:  2000-06       Impact factor: 4.296

2.  Patterns of decline in upper limb function of boys and men with DMD: an international survey.

Authors:  Mariska M H P Janssen; Arjen Bergsma; Alexander C H Geurts; Imelda J M de Groot
Journal:  J Neurol       Date:  2014-04-01       Impact factor: 4.849

Review 3.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; David Brumbaugh; Laura E Case; Paula R Clemens; Stasia Hadjiyannakis; Shree Pandya; Natalie Street; Jean Tomezsko; Kathryn R Wagner; Leanne M Ward; David R Weber
Journal:  Lancet Neurol       Date:  2018-02-03       Impact factor: 44.182

4.  Early signs of gait deviation in Duchenne muscular dystrophy.

Authors:  L Doglio; E Pavan; I Pernigotti; P Petralia; C Frigo; C Minetti
Journal:  Eur J Phys Rehabil Med       Date:  2011-09-13       Impact factor: 2.874

5.  Serial casting for the management of ankle contracture in Duchenne muscular dystrophy.

Authors:  Allan M Glanzman; Jean M Flickinger; Kripa H Dholakia; Carsten G Bönnemann; Richard S Finkel
Journal:  Pediatr Phys Ther       Date:  2011       Impact factor: 3.049

6.  Muscle ultrasound elastography and MRI in preschool children with Duchenne muscular dystrophy.

Authors:  Anna Pichiecchio; Francesco Alessandrino; Chandra Bortolotto; Alessandra Cerica; Cristina Rosti; Maria Vittoria Raciti; Marta Rossi; Angela Berardinelli; Giovanni Baranello; Stefano Bastianello; Fabrizio Calliada
Journal:  Neuromuscul Disord       Date:  2018-04-13       Impact factor: 4.296

7.  Skeletal muscle water T2 as a biomarker of disease status and exercise effects in patients with Duchenne muscular dystrophy.

Authors:  Ami Mankodi; Noura Azzabou; Thomas Bulea; Harmen Reyngoudt; Hirity Shimellis; Yupeng Ren; Eunhee Kim; Kenneth H Fischbeck; Pierre G Carlier
Journal:  Neuromuscul Disord       Date:  2017-04-28       Impact factor: 4.296

8.  Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging.

Authors:  Franklin A Marden; Anne M Connolly; Marilyn J Siegel; David A Rubin
Journal:  Skeletal Radiol       Date:  2004-10-22       Impact factor: 2.199

9.  Longitudinal measurements of MRI-T2 in boys with Duchenne muscular dystrophy: effects of age and disease progression.

Authors:  R J Willcocks; I A Arpan; S C Forbes; D J Lott; C R Senesac; E Senesac; J Deol; W T Triplett; C Baligand; M J Daniels; H L Sweeney; G A Walter; K Vandenborne
Journal:  Neuromuscul Disord       Date:  2014-01-11       Impact factor: 4.296

10.  The effect of wearing night splints for one year on the standing motor function of patients with Duchenne muscular dystrophy.

Authors:  Hitomi Nishizawa; Ayumi Matsukiyo; Naoko Shiba; Masayoshi Koinuma; Akinori Nakamura
Journal:  J Phys Ther Sci       Date:  2018-04-20
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  1 in total

1.  Development of Contractures in DMD in Relation to MRI-Determined Muscle Quality and Ambulatory Function.

Authors:  Rebecca J Willcocks; Alison M Barnard; Ryan J Wortman; Claudia R Senesac; Donovan J Lott; Ann T Harrington; Kirsten L Zilke; Sean C Forbes; William D Rooney; Dah-Jyuu Wang; Erika L Finanger; Gihan I Tennekoon; Michael J Daniels; William T Triplett; Glenn A Walter; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2022
  1 in total

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