Analysis: Systemic Sclerosis and Systemic Lupus Erythematous Overlap

By Kaitlyn D’Onofrio - Last Updated: October 23, 2018

A cohort study published in The Journal of Rheumatology analyzed factors associated with combination systemic sclerosis (SSc) and systemic lupus erythematous (SLE). 

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Participants were included if they met the American College of Rheumatology (ACR)/European League Against Rheumatism classification criteria for SSc and/or the ACR criteria for SLE. A total of 1,252 subjects met the criteria (SSc: n = 1,166), of which 86 (6.8%) had SSc and SLE. Risk factors for SSc-SLE were younger age at diagnosis (37.9 vs 47.9 years, < 0.001); East Asian (5.5% vs 20%) or South Asian (5.1% vs 12%) descent; and presence of lupus anticoagulant (6% vs 0.3%, P < 0.001), anticardiolipin antibody (6% vs 0.9%, P < 0.001), and pulmonary arterial hypertension (52% vs 31%, P < 0.001). 

SSc-SLE combination patients had lower incidences of calcinosis (13% vs 27%, P = 0.007), telangiectasia (49% vs 75%, P < 0.001), and diffuse subtype (12% vs 35%, P < 0.001). Researchers did not observe significant differences between SSc-SLE and SSc patients in occurrence of renal crisis (7% vs 7%), interstitial lung disease (ILD) (41% vs 34%), and digital ulcers (38% vs 32%). Median survival time was greater but not significantly so in SSc-SLE patients (26.1 vs 22.4 years, log-rank P = 0.06). 

In their conclusion the authors recommended that SSc-SLE patients “be monitored for ILD, renal crisis, and digital ulcers.” 

Epidemiology and Survival of Systemic Sclerosis-Systemic Lupus Erythematosus Overlap Syndrome 

Systemic Sclerosis Diagnosis: What Are the Risk Factors for Future Scleroderma Renal Crisis? 

Study: Strong Reproducibility in 6-Minute Walk Test for Systemic Sclerosis

Source: The Journal of Rheumatology

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