Literature DB >> 34536384

Characterizing Expiratory Respiratory Muscle Degeneration in Duchenne Muscular Dystrophy Using MRI.

Alison M Barnard1, Donovan J Lott1, Abhinandan Batra1, William T Triplett1, Rebecca J Willcocks1, Sean C Forbes1, William D Rooney2, Michael J Daniels3, Barbara K Smith1, Krista Vandenborne1, Glenn A Walter4.   

Abstract

BACKGROUND: Expiratory muscle weakness and impaired airway clearance are early signs of respiratory dysfunction in Duchenne muscular dystrophy (DMD), a degenerative muscle disorder in which muscle cells are damaged and replaced by fibrofatty tissue. Little is known about expiratory muscle pathology and its relationship to cough and airway clearance capacity; however, the level of muscle replacement by fat can be estimated using MRI and expressed as a fat fraction (FF). RESEARCH QUESTION: How does abdominal expiratory muscle fatty infiltration change over time in DMD and relate to clinical expiratory function? STUDY DESIGN AND METHODS: Individuals with DMD underwent longitudinal MRI of the abdomen to determine FF in the internal oblique, external oblique, and rectus abdominis expiratory muscles. FF data were used to estimate a model of expiratory muscle degeneration by using nonlinear mixed effects and a cumulative distribution function. FVC, maximal inspiratory and expiratory pressures, and peak cough flow were collected as clinical correlates to MRI.
RESULTS: Forty individuals with DMD (aged 6-18 years at baseline) participated in up to five visits over 36 months. Modeling estimated the internal oblique progresses most quickly and reached 50% replacement by fat at a mean patient age of 13.0 years (external oblique, 14.0 years; rectus abdominis, 16.2 years). Corticosteroid-untreated individuals (n = 4) reached 50% muscle replacement by fat 3 to 4 years prior to treated individuals. Individuals with mild clinical dystrophic phenotypes (n = 3) reached 50% muscle replacement by fat 4 to 5 years later than corticosteroid-treated individuals. Internal and external oblique FFs near 50% were associated with maximal expiratory pressures < 60 cm H2O and peak cough flows < 270 L/min.
INTERPRETATION: These data improve understanding of the early phase of respiratory compromise in DMD, which typically presents as airway clearance dysfunction prior to the onset of hypoventilation, and links expiratory muscle fatty infiltration to pulmonary function measures.
Copyright © 2021 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Duchenne muscular dystrophy; MRI; airway clearance; cough; expiratory muscles

Mesh:

Substances:

Year:  2021        PMID: 34536384      PMCID: PMC9160975          DOI: 10.1016/j.chest.2021.08.078

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   10.262


  34 in total

Review 1.  Pulmonary function and clinical correlation in DMD.

Authors:  Oscar H Mayer
Journal:  Paediatr Respir Rev       Date:  2018-09-13       Impact factor: 2.726

2.  Evidence-based care in Duchenne muscular dystrophy.

Authors:  Craig M McDonald; Eugenio Mercuri
Journal:  Lancet Neurol       Date:  2018-05       Impact factor: 44.182

3.  Imaging respiratory muscle quality and function in Duchenne muscular dystrophy.

Authors:  Alison M Barnard; Donovan J Lott; Abhinandan Batra; William T Triplett; Sean C Forbes; Samuel L Riehl; Rebecca J Willcocks; Barbara K Smith; Krista Vandenborne; Glenn A Walter
Journal:  J Neurol       Date:  2019-07-26       Impact factor: 4.849

Review 4.  Airway clearance techniques in neuromuscular disorders: A state of the art review.

Authors:  Michelle Chatwin; Michel Toussaint; Miguel R Gonçalves; Nicole Sheers; Uwe Mellies; Jesus Gonzales-Bermejo; Jesus Sancho; Brigitte Fauroux; Tiina Andersen; Brit Hov; Malin Nygren-Bonnier; Matthieu Lacombe; Kurt Pernet; Mike Kampelmacher; Christian Devaux; Kathy Kinnett; Daniel Sheehan; Fabrizio Rao; Marcello Villanova; David Berlowitz; Brenda M Morrow
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5.  Respiratory Management of the Patient With Duchenne Muscular Dystrophy.

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8.  Modeling disease trajectory in Duchenne muscular dystrophy.

Authors:  William D Rooney; Yosef A Berlow; William T Triplett; Sean C Forbes; Rebecca J Willcocks; Dah-Jyuu Wang; Ishu Arpan; Harneet Arora; Claudia Senesac; Donovan J Lott; Gihan Tennekoon; Richard Finkel; Barry S Russman; Erika L Finanger; Saptarshi Chakraborty; Elliott O'Brien; Brendan Moloney; Alison Barnard; H Lee Sweeney; Michael J Daniels; Glenn A Walter; Krista Vandenborne
Journal:  Neurology       Date:  2020-03-17       Impact factor: 9.910

9.  Respiratory muscle strength and cough capacity in patients with Duchenne muscular dystrophy.

Authors:  Seong-Woong Kang; Yeoun-Seung Kang; Hong-Seok Sohn; Jung-Hyun Park; Jae-Ho Moon
Journal:  Yonsei Med J       Date:  2006-04-30       Impact factor: 2.759

10.  Very Low Residual Dystrophin Quantity Is Associated with Milder Dystrophinopathy.

Authors:  Yvan de Feraudy; Rabah Ben Yaou; Karim Wahbi; Caroline Stalens; Amalia Stantzou; Vincent Laugel; Isabelle Desguerre; Laurent Servais; France Leturcq; Helge Amthor
Journal:  Ann Neurol       Date:  2020-11-24       Impact factor: 10.422

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Review 1.  Breathing in Duchenne muscular dystrophy: translation to therapy.

Authors:  Doreen Z Mhandire; David P Burns; Angela L Roger; Ken D O'Halloran; Mai K ElMallah
Journal:  J Physiol       Date:  2022-06-24       Impact factor: 6.228

  1 in total

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