Short Form-36 psychometric properties in idiopathic inflammatory myopathies: Reliability, validity and responsiveness
Issued Date
2025-08-01
Resource Type
ISSN
14620324
eISSN
14620332
Scopus ID
2-s2.0-105012363154
Pubmed ID
40279268
Journal Title
Rheumatology
Volume
64
Issue
8
Start Page
4695
End Page
4702
Rights Holder(s)
SCOPUS
Bibliographic Citation
Rheumatology Vol.64 No.8 (2025) , 4695-4702
Suggested Citation
Keret S., Aggarwal A., Almackenzie M., Bijoy George T., Sriram S., Chandra T., Lomanto Silva R., Gkiaouraki E., Pongtarakulpanit N., Moghadam-Kia S., Oddis C.V., Aggarwal R. Short Form-36 psychometric properties in idiopathic inflammatory myopathies: Reliability, validity and responsiveness. Rheumatology Vol.64 No.8 (2025) , 4695-4702. 4702. doi:10.1093/rheumatology/keaf219 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/111681
Title
Short Form-36 psychometric properties in idiopathic inflammatory myopathies: Reliability, validity and responsiveness
Corresponding Author(s)
Other Contributor(s)
Abstract
Objective To evaluate the psychometric properties of Short Form-36 (SF-36) as a health-related quality of life (HRQoL) measure in idiopathic inflammatory myopathies (IIMs). Methods Patients fulfilling the EULAR/ACR classification criteria or with myositis-specific antibodies were enrolled from two clinical trials (Tocilizumab in Myositis and Abatacept in Myositis) and one prospective observational study. Data collection at 0, 3 and 6 months included all myositis core set measures (CSMs) including manual muscle testing-8 (MMT-8), and SF-36 summary scores and all eight subdomains including physical component summary score (PCS) and physical function. Test-retest reliability (Pearson correlation), validity (association with other valid measures) and responsiveness using clinically important difference (CID) and effect size were calculated. Results The study included 105 IIM patients (44% DM, 30% anti-synthetase syndrome, 18% PM, 8% necrotizing myopathy), with mean age: 52.3 years, 64% females and 85% White. HRQoL scores were significantly lower in IIM compared with the general population. All SF-36 domain scores were significantly lower in patients with active disease and muscle weakness. All SF-36 components demonstrated good test-retest reliability at 1 month (P < 0.001), with significant baseline and longitudinal associations with most myositis CSMs. Changes in MMT-8 strongly correlated with changes in PCS and physical domains. PCS illustrated significant and concordant change with 2016 ACR/EULAR myositis response criteria and physician/patient assessments of change, showing a large effect size. We present preliminary CIDs based on a cohort with minimal clinical change. Conclusion SF-36 demonstrates good reliability, validity and responsiveness in IIM and should be utilized for assessing HRQoL in clinical practice and myositis trials.