Analysis of motor and respiratory function in Duchenne muscular dystrophy patients.
Respir Physiol Neurobiol
; 262: 1-11, 2019 04.
Article
in En
| MEDLINE
| ID: mdl-30660861
ABSTRACT
INTRODUCTION:
Duchenne muscular dystrophy(DMD) shows motor and respiratory impairment.METHODS:
19 DMD patients (DMDG) (nine ambulatory and 10 non-ambulatory) were evaluated through motor function measure (MFM), 6-minute walk test (6MWT), respiratory muscle strength, cough peak flow, spirometry and volumetric capnography (VCap) tools. Control group that performed spirometry and VCap (CG1-n = 17) were different from those that performed the 6MWT (CG2-n = 8).RESULTS:
The follow tools were assessed (p < 0.05) (i) MFM Ambulatory patients showed higher values than non-ambulatory patients; (ii) 6MWT DMDG walked a shorter distance and showed higher respiratory rate at rest and heart rate (HR) at rest than CG2; (iii) Spirometry DMDG and non-ambulatory patients had minor values achieved in spirometry when compared with CG1 and ambulatory patients, respectively; (iv) VCap DMDG when compared with CG1 showed (<11 years-old) lower values in VCap parameters; (>11 years-old) higher HR and lower slope 2. There was correlation between spirometry, mainly for zFEV1/FVC, and MFM.CONCLUSION:
DMDG showed motor (MFM/6MWT) and respiratory (spirometry/VCap) deterioration when compared with CG. Non-ambulatory condition was associated with worse MFM and spirometry.Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Respiration
/
Muscular Dystrophy, Duchenne
/
Motor Activity
Type of study:
Etiology_studies
/
Observational_studies
/
Prevalence_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Child
/
Humans
/
Male
Language:
En
Journal:
Respir Physiol Neurobiol
Year:
2019
Document type:
Article