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  3. Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: A cross-sectional analysis.

Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: A cross-sectional analysis.

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DOI
10.7892/boris.111147
Publisher DOI
10.1016/j.nmd.2017.10.003
PubMed ID
29174526
Abstract
The development of new therapeutic agents for the treatment of Duchenne muscular dystrophy has put a focus on defining outcome measures most sensitive to capture treatment effects. This cross-sectional analysis investigates the relation between validated clinical assessments such as the 6-minute walk test, motor function measure and quantitative muscle MRI of thigh muscles in ambulant Duchenne muscular dystrophy patients, aged 6.5 to 10.8 years (mean 8.2, SD 1.1). Quantitative muscle MRI included the mean fat fraction using a 2-point Dixon technique, and transverse relaxation time (T2) measurements. All clinical assessments were highly significantly inter-correlated with p < 0.001. The strongest correlation with the motor function measure and its D1-subscore was shown by the 6-minute walk test. Clinical assessments showed no correlation with age. Importantly, quantitative muscle MRI values significantly correlated with all clinical assessments with the extensors showing the strongest correlation. In contrast to the clinical assessments, quantitative muscle MRI values were highly significantly correlated with age. In conclusion, the motor function measure and timed function tests measure disease severity in a highly comparable fashion and all tests correlated with quantitative muscle MRI values quantifying fatty muscle degeneration.
Date Issued
2018-01
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
6-minute walk distance 6-minute walk test Duchenne muscular dystrophy Imaging biomarkers Motor function measure Quantitative MRI Timed function tests
Language(s)
en
Author(s)
Schmidt, Simone
Hafner, Patricia
Klein, Andrea Katharina  
Universitätsklinik für Kinderheilkunde, Neuropädiatrie  
Rubino-Nacht, Daniela
Gocheva, Vanya
Schroeder, Jonas
Naduvilekoot Devasia, Arjith
Zuesli, Stephanie
Bernert, Guenther
Laugel, Vincent
Bloetzer, Clemens
Steinlin, Maja  
Universitätsklinik für Kinderheilkunde  
Capone, Andrea
Gloor, Monika
Tobler, Patrick
Haas, Tanja
Bieri, Oliver
Zumbrunn, Thomas
Fischer, Dirk
Bonati, Ulrike
Additional Credits
Universitätsklinik für Kinderheilkunde, Neuropädiatrie  
Universitätsklinik für Kinderheilkunde  
Journal
Neuromuscular disorders
Publisher
Elsevier
ISSN
0960-8966
Access(Rights)
restricted
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