Systemic sclerosis & Raynaud's

Evaluation of a screening algorithm to detect systemic sclerosis-related myopathy

Rheumatology (Oxford)Published Cohort study

Authors' conclusion

Biopsy-proven muscle involvement was identified in 9.9% of screened SSc patients, and detection of IM increased by ∼4.5-fold compared with routine care

Study context

Population
Consecutive Systemic Sclerosis (SSc) patients in the Australian Scleroderma Cohort Studymedian follow-up 5.19 years
Participants
1,443 patients
Exposure
Proposed screening algorithm vs routine care
Outcome
Biopsy-proven SSc-related myopathy (inflammatory myopathy)
Methodological detailsconsecutive patients, annual assessment, screening algorithm applied in a subset (South Australia)
  • Consecutive patients
  • Annual assessment
  • Screening algorithm applied in a subset (South Australia)

Main finding

As reported in the abstract

Biopsy-proven IM

Observational data: associations, not effects.

Further findings

Biopsy-proven myopathy during routine care, whole cohort · median follow-up 5.19 years

26/1253 had biopsy-proven myopathy
2.1%
Biopsy-proven inflammatory myopathy (IM)
1.4%

Weakness and elevated creatine kinase (CK) at least once during routine care, whole cohort · median follow-up 5.19 years

Weakness, 260/1407
18.5%
Elevated CK, 203/1282
15.8%

South Australia (SA) patients: weakness, elevated CK and muscle biopsy based on a positive screen

Weakness, 117/425
27.5%
Elevated CK, 80/421
19%
Muscle biopsy after positive screen, 42/423
9.9%
Positive screen from weakness and/or elevated CK
n = 48
Positive screen from myositis-specific/myositis-associated autoantibodies
n = 10
Positive screen from MRI abnormalities
n = 8

SA biopsy findings

All 42 biopsies abnormal; IM, 28/42
66.7%
Non-specific myopathic changes, 14/42
33.3%

Original publication

Evaluation of a screening algorithm to detect systemic sclerosis-related myopathy. Rheumatology (Oxford). Published 28 January 2026. doi:10.1093/rheumatology/keaf688

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