Systemic sclerosis & Raynaud's

Late‐Onset Scleroderma Renal Crisis Does Occur—A Multicenter Study

Arthritis Care Res (Hoboken)Published Retrospective cohort study

Authors' conclusion

Late-onset SRC was seen in up to 25% of patients with SRC, with a mean of 12 years after SSc diagnosis. Our findings reveal comparable clinical characteristics and outcomes between early- and late-onset SRC

Study context

Population
Patients diagnosed with scleroderma renal crisis (SRC) in systemic sclerosis (SSc), 1995–2018, three university-affiliated hospitals
Participants
223 patients
Exposure
Late-onset vs early-onset scleroderma renal crisis
  • Late onsetn = 54
  • Early onsetn = 169reference
Outcome
Prevalence, clinical features and outcomes of late-onset SRC vs early-onset SRC
Methodological detailsmulticentre, three university-affiliated hospitals
  • Multicentre
  • Three university-affiliated hospitals

Main finding

As reported in the abstract

Prevalence of late- vs early-onset SRC

Observational data: associations, not effects.

Further findings

Male sex

OutcomeLate onsetEarly onset
Time from SSc diagnosis to SRC onset, late-onset SRCmean 12.2 years— not stated in the abstract

— not stated in the abstract

Steroid exposure, late-onset vs early-onset SRC

Steroid exposure more common in late-onset (late group 56%) than early-onset (early group 29%)

Autoantibody profile and outcomes

No evidence of difference between early- and late-onset groups

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Late‐Onset Scleroderma Renal Crisis Does Occur—A Multicenter Study. Arthritis Care Res (Hoboken). Published 18 November 2025. doi:10.1002/acr.25608

Composed by AI from the published abstract and checked against it. How Briefs are made →

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