Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial

Male info:eu-repo/classification/mesh/Young Adult [SDV]Life Sciences [q-bio] Mesh:Muscular Dystrophy Mesh:Adult Mesh:Adolescent 0302 clinical medicine info:eu-repo/classification/mesh/Female Mesh:Duchenne/drug therapy Muscular Dystrophy Mesh:Muscle Strength*/drug effects info:eu-repo/classification/mesh/Child Child Mesh:Duchenne/physiopathology* info:eu-repo/classification/mesh/Adult info:eu-repo/classification/mesh/Follow-Up Studies info:eu-repo/classification/mesh/Muscle Strength*/drug effects Q R Mesh:Recovery of Function*/drug effects Sciences bio-médicales et agricoles 3. Good health [SDV] Life Sciences [q-bio] info:eu-repo/classification/mesh/Muscular Dystrophy Medicine Female info:eu-repo/classification/mesh/Male Research Article Mesh:Follow-Up Studies Mesh:Female Adult info:eu-repo/classification/mesh/Duchenne/drug therapy Mesh:Child Adolescent Science 610 Mesh:Male Mesh:Young Adult Upper Extremity Young Adult 03 medical and health sciences Upper Extremity -- physiopathology Muscular Dystrophy, Duchenne -- drug therapy -- physiopathology 617 Humans Muscle Strength Recovery of Function -- drug effects info:eu-repo/classification/mesh/Adolescent Recovery of Function Muscular Dystrophy, Duchenne Mesh:Humans info:eu-repo/classification/mesh/Duchenne/physiopathology* Muscle Strength -- drug effects Mesh:Upper Extremity/physiopathology* Duchenne -- drug therapy -- physiopathology info:eu-repo/classification/mesh/Recovery of Function*/drug effects info:eu-repo/classification/mesh/Humans info:eu-repo/classification/mesh/Upper Extremity/physiopathology* Follow-Up Studies
DOI: 10.1371/journal.pone.0113999 Publication Date: 2015-02-02T20:14:09Z
ABSTRACT
Upper limb evaluation of patients with Duchenne Muscular Dystrophy is crucially important to evaluations of efficacy of new treatments in non-ambulant patients. In patients who have lost ambulation, there are few validated and informative outcome measures. In addition, longitudinal data demonstrating sensitivity to clinical evolution of outcome measures over short-term periods are lacking.We report here the results of a one-year multicenter study using specifically designed tools to assess grip, pinch strength, and hand function in wheelchair-bound patients. Our study assessed 53 non-ambulant patients with Duchenne muscular dystrophy aged 17.1 ± 4.8 years (range: 9 - 28.1 years). The average Brooke functional score of these patients was 4.6 ± 1.1. The average forced vital capacity was 44.5% predicted and 19 patients used non-invasive ventilation. Patients were assessed at baseline, 6 months, and one year using the Motor Function Measure and innovative devices (namely the MyoSet composed of MyoGrip, MyoPinch, and MoviPlate).Our study confirmed preliminary data previously reported regarding feasibility of use and of reliability of the MyoSet and the correlation at baseline between distal strength and clinical outcomes such as FVC, Brooke score, age, and duration since loss of ambulation. A significant correlation was observed between the distal upper limb strength and clinical variables. The sensitive dynamometers (MyoGrip and MyoPinch) and MoviPlate captured a 12-month change in non-ambulant Duchenne muscular dystrophy patients of all ages.ClinicalTrials.gov NCT00993161 NCT00993161.
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