Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis
Authors:
- M. O. Harris-LoveMHM. O. Harris-Love
- J. A. ShraderJSJ. A. Shrader
- D. KoziolDKD. Koziol
- N. PahlajaniNPN. Pahlajani
- M. JainMJM. Jain
- M. SmithMSM. Smith
- H. L. CintasHCH. L. Cintas
- C. L. McGarveyCMC. L. McGarvey
- L. James-NewtonLJL. James-Newton
- A. PokrovnichkaAPA. Pokrovnichka
- B. MoiniBMB. Moini
- I. CabalarICI. Cabalar
Open Access
- 11 December 2008
- journal article
- research article
- Published by Oxford University Press (OUP) in Rheumatology
- Vol. 48 (2) , 134-139
Abstract
Objective. To describe the distribution and severity of muscle weakness using manual muscle testing (MMT) in 172 patients with PM, DM and juvenile DM (JDM). The secondary objectives included characterizing individual muscle group weakness and determining associations of weakness with functional status and myositis characteristics in this large cohort of patients with myositis. Methods. Strength was assessed for 13 muscle groups using the 10-point MMT and expressed as a total score, subscores based on functional and anatomical regions, and grades for individual muscle groups. Patient characteristics and secondary outcomes, such as clinical course, muscle enzymes, corticosteroid dosage and functional status were evaluated for association with strength using univariate and multivariate analyses. Results. A gradient of proximal weakness was seen, with PM weakest, DM intermediate and JDM strongest among the three myositis clinical groups (P ≤ 0.05). Hip flexors, hip extensors, hip abductors, neck flexors and shoulder abductors were the muscle groups with the greatest weakness among all three clinical groups. Muscle groups were affected symmetrically. Conclusions. Axial and proximal muscle impairment was reflected in the five weakest muscles shared by our cohort of myositis patients. However, differences in the pattern of weakness were observed among all three clinical groups. Our findings suggest a greater severity of proximal weakness in PM in comparison with DM.Keywords
This publication has 42 references indexed in Scilit:
- Long-term outcome in polymyositis and dermatomyositisAnnals of the Rheumatic Diseases, 2006
- Prognosis and mortality of polymyositis and dermatomyositis patientsClinical Rheumatology, 2006
- Survival, mortality and causes of death in inflammatory myopathiesAutoimmunity, 2006
- Intra-Rater and Inter-Rater Reliability of the 10-Point Manual Muscle Test (MMT) of Strength in Children with Juvenile Idiopathic Inflammatory Myopathies (JIIM)Physical & Occupational Therapy In Pediatrics, 2006
- Retrospective Review of the Clinical Manifestations and Outcomes in Puerto Ricans with Idiopathic Inflammatory MyopathiesJCR: Journal of Clinical Rheumatology, 2005
- Adult‐onset inflammatory myopathy: North Canterbury experience 1989–2001Internal Medicine Journal, 2005
- Functional outcome and quality of life in adult patients with idiopathic inflammatory myositisRheumatology, 2005
- Adult inflammatory myopathiesBest Practice & Research Clinical Rheumatology, 2004
- The Relationship of Strength to Function in the Older AdultThe Journals of Gerontology, Series A: Biological Sciences and Medical Sciences, 1995
- Muscles, Testing and FunctionMedicine & Science in Sports & Exercise, 1994