Literature DB >> 23836708

Respiratory muscle decline in Duchenne muscular dystrophy.

Sonia Khirani1, Adriana Ramirez, Guillaume Aubertin, Michèle Boulé, Chrystelle Chemouny, Véronique Forin, Brigitte Fauroux.   

Abstract

OBJECTIVES: Duchenne muscular dystrophy (DMD) causes progressive respiratory muscle weakness. The aim of the study was to analyze the trend of a large number of respiratory parameters to gain further information on the course of the disease. STUDY
DESIGN: Retrospective study. SUBJECT SELECTION: 48 boys with DMD, age range between 6 and 19 year old, who were followed in our multidisciplinary neuromuscular clinic between 2001 and 2011.
METHODOLOGY: Lung function, blood gases, respiratory mechanics, and muscle strength were measured during routine follow-up over a 10-year period. Only data from patients with at least two measurements were retained.
RESULTS: The data of 28 patients were considered for analysis. Four parameters showed an important decline with age. Gastric pressure during cough (Pgas cough) was below normal in all patients with a mean decline of 5.7 ± 3.8 cmH2 O/year. Sniff nasal inspiratory pressure (SNIP) tended to increase first followed by a rapid decline (mean decrease 4.8 ± 4.9 cmH2 O; 5.2 ± 4.4% predicted/year). Absolute forced vital capacity (FVC) values peaked around the age of 13-14 years and remained mainly over 1 L but predicted values showed a mean 4.1 ± 4.4% decline/year. Diaphragmatic tension-time index (TTdi) increased above normal values after the age of 14 years with a mean increase of 0.04 ± 0.04 point/year.
CONCLUSIONS: This study confirms the previous findings that FVC and SNIP are among the most important parameters to monitor the evolution of DMD. Expiratory muscle strength, assessed by Pgas cough, and the endurance index, TTdi, which are reported for the first time in a large cohort, appeared to be informative too, even though measured through an invasive method.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  Duchenne muscular dystrophy; longitudinal study; muscles strength; pulmonary function

Mesh:

Year:  2013        PMID: 23836708     DOI: 10.1002/ppul.22847

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  33 in total

1.  Inspiratory pressure-generating capacity is preserved during ventilatory and non-ventilatory behaviours in young dystrophic mdx mice despite profound diaphragm muscle weakness.

Authors:  David P Burns; Kevin H Murphy; Eric F Lucking; Ken D O'Halloran
Journal:  J Physiol       Date:  2019-01-13       Impact factor: 5.182

2.  Sensorimotor control of breathing in the mdx mouse model of Duchenne muscular dystrophy.

Authors:  David P Burns; Arijit Roy; Eric F Lucking; Fiona B McDonald; Sam Gray; Richard J Wilson; Deirdre Edge; Ken D O'Halloran
Journal:  J Physiol       Date:  2017-10-09       Impact factor: 5.182

3.  Proteomic profiling of the mouse diaphragm and refined mass spectrometric analysis of the dystrophic phenotype.

Authors:  Sandra Murphy; Margit Zweyer; Maren Raucamp; Michael Henry; Paula Meleady; Dieter Swandulla; Kay Ohlendieck
Journal:  J Muscle Res Cell Motil       Date:  2019-03-19       Impact factor: 2.698

4.  Systemic AAV-Mediated β-Sarcoglycan Delivery Targeting Cardiac and Skeletal Muscle Ameliorates Histological and Functional Deficits in LGMD2E Mice.

Authors:  Eric R Pozsgai; Danielle A Griffin; Kristin N Heller; Jerry R Mendell; Louise R Rodino-Klapac
Journal:  Mol Ther       Date:  2017-03-09       Impact factor: 11.454

5.  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 6.  Update on muscle disease.

Authors:  J Witherick; S Brady
Journal:  J Neurol       Date:  2018-04-18       Impact factor: 4.849

Review 7.  Sleep Disordered Breathing in Duchenne Muscular Dystrophy.

Authors:  Antonella LoMauro; Maria Grazia D'Angelo; Andrea Aliverti
Journal:  Curr Neurol Neurosci Rep       Date:  2017-05       Impact factor: 5.081

8.  Respiratory functional and motor control deficits in children with spinal cord injury.

Authors:  Goutam Singh; Andrea L Behrman; Sevda C Aslan; Shelley Trimble; Alexander V Ovechkin
Journal:  Respir Physiol Neurobiol       Date:  2017-10-28       Impact factor: 1.931

9.  Recovery of respiratory function in mdx mice co-treated with neutralizing interleukin-6 receptor antibodies and urocortin-2.

Authors:  David P Burns; Leonie Canavan; Jane Rowland; Robin O'Flaherty; Molly Brannock; Sarah E Drummond; Dervla O'Malley; Deirdre Edge; Ken D O'Halloran
Journal:  J Physiol       Date:  2018-10-03       Impact factor: 5.182

Review 10.  Respiratory assessment in centronuclear myopathies.

Authors:  Barbara K Smith; Melissa Goddard; Martin K Childers
Journal:  Muscle Nerve       Date:  2014-08-05       Impact factor: 3.217

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