Outcome in Patients With Recent Onset Polymyositis and Dermatomyositis

Sponsor
Karolinska University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01813617
Collaborator
(none)
72
1

Study Details

Study Description

Brief Summary

Most patients respond to medical treatment with corticosteroids and immunosuppressive treatment, but a majority of patients develop sustained muscle impairment. The aim of this study was to evaluate the outcome of muscle endurance assessed with the Functional Index-2 (FI-2), muscle strength assessed by the MMT-8 and disease activity assessed by the six item core set at 6 and 12 months following diagnosis in patients with polymyositis (PM) and dermatomyositis (DM).

72 patients diagnosed with probable or definite PM or DM 2003-2010 who performed the FI-2 and the MMT at the time of diagnosis were included in this Swedish Myositis Register study. All patients had performed both the Functional Index-2 assessing muscle endurance and the Manual Muscle test (MMT) assessing isometric muscle strength. Physician Global assessment based on the evaluation of the consensus recommended six item core set for disease activity assessment was also included. Data were analysed on group levels as well as with criteria for individual responder criteria. A responder was identified as improving at least 20 % compared to baseline.

Condition or Disease Intervention/Treatment Phase
  • Drug: Immunosuppressive Agents

Detailed Description

The purpose of this study was to investigate the degree of impairment of isometric muscle weakness and dynamic muscle endurance in patients with recent onset PM and DM and to evaluate how muscle impairment and disease activity changes during the first year following diagnosis of PM or DM. A further aim was to investigate the association between muscle impairment, disease activity and autoantibodies in these patients.

All patients diagnosed with definite or probable PM or DM according to Bohan and Peter criteria (Bohan and Peter 1975) 2003-2010, at the Rheumatology clinic at Karolinska University Hospital, also included in the Swedish Rheumatology Register (SweMyoNet) who had performed measures of dynamic muscle endurance by the FI-2 and isometric muscle strength by the MMT-8 were included in this register study (n=71).

Functional Index-2 is a disease specific, valid and reliable instrument assessing muscular endurance in seven muscle groups including seven tasks; shoulder flexion, shoulder abduction, neck flexion, hip flexion, step test and toe lifts and heel lifts. Each muscle group are scored as the number of correctly executed repetitions.

The six-item core set for measures of disease activity include; Physician's and patient's assessment of disease activity on a Visual Analogue Scale (VAS), the Manual Muscle Test (MMT), the Stanford Health Assessment Questionnaire (HAQ), analyses of muscle enzymes and the extra-muscular disease activity scores Myositis Disease Activity Visual Analogue Scales (MYOACT) or the Myositis Intention to Treat Index (MITAX). The 8-muscle group MMT was performed on the dominant body side including muscle groups; neck flexors, deltoids, biceps brachia, dorsi flexors of the wrist, gluteus maximus and medius, quadriceps and dorsi flexors of the ankle. Total score varies between 0 and 80, where 80 indicate normal muscular strength.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
72 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Outcome of Muscle Function and Disease Activity in Patients With Recent Onset Polymyositis and Dermatomyositis - a 1-year Follow-up Register Study
Study Start Date :
Sep 1, 2010
Actual Primary Completion Date :
Jun 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Recent onset polymyositis and dermatomyositis

Patients in this cohort was diagnosed with polymyositis or dermatomyositis during 2003-2010 and was treated with corticosteroids and other immunosuppressive agents according to standard care. They were all diagnosed and treated at the Rheumatology Clinic, Karolinska University Hospital.

Drug: Immunosuppressive Agents
Patients in the cohort received medical treatment according to standard care.
Other Names:
  • Prednisone
  • Methotrexate
  • Azathioprine
  • Outcome Measures

    Primary Outcome Measures

    1. Functional Index 2 assessing change in muscle function over time. [0, 6 and 12 months]

      The FI-2 is a disease-specific assessment of dynamic muscle endurance in 7 muscle groups and records the number of correct performed repetitions for each muscle group.

    Secondary Outcome Measures

    1. Manual Muscle test, MMT-8, assessing change in muscle function over time. [0, 6 and 12 months]

      Measure isometric muscle strength in 8 muscle groups and is scored between 0-10 for each muscle group with a total score of 80 indicating godd muscle strength.

    Other Outcome Measures

    1. Physicians global assessment of disease activity assessing change over time. [0, 6 and 12 months]

      Physician's global assessment is included in the consensus proposed six item core set of disease activity measures also including patient's global assessment, the MMT, Health Assessment Questionnaire (HAQ), analysis of muscle enzymes and the extra-muscular disease activity tools MITAX or MYOACT.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Probable or definite polymyositis and dermatomyositis

    • Performed both the FI-2 and the MMT at time of diagnosis

    Exclusion Criteria:
    • Patients with diagnosis inclusions body myositis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Karolinska University Hospital, Solna Stockholm Sweden 171 76

    Sponsors and Collaborators

    • Karolinska University Hospital

    Investigators

    • Principal Investigator: Helene Alexanderson, PhD, RPT, Karolinska University Hospital / Karolinska Institutet

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Helene Alexanderson, PhD, RPT, Karolinska University Hospital
    ClinicalTrials.gov Identifier:
    NCT01813617
    Other Study ID Numbers:
    • SweMyoNet 1
    • Centre of Care Science
    First Posted:
    Mar 19, 2013
    Last Update Posted:
    Mar 19, 2013
    Last Verified:
    Mar 1, 2013
    Keywords provided by Helene Alexanderson, PhD, RPT, Karolinska University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 19, 2013