Core Concepts
Patients with systemic sclerosis (SSc) and systemic lupus erythematosus (SLE) exhibit overlapping characteristics, emphasizing the need for recognition and monitoring of this syndrome.
Abstract
TOPLINE:
Patients with both SSc and SLE are more likely to be female, Black, and diagnosed with limited cutaneous SSc.
METHODOLOGY:
Used 2019 SLE classification criteria to identify patients with SSc meeting SLE criteria.
Study included 402 adults with SSc.
TAKEAWAY:
10% of SSc patients met 2019 EULAR/ACR Classification Criteria for SLE.
Patients with both conditions more likely to be female, Black, and have limited cutaneous SSc.
Anti-U1-RNP antibody positivity higher in SSc-SLE patients.
IN PRACTICE:
Clinicians should recognize SSc-SLE overlap syndrome and monitor for organ involvement.
SOURCE:
Study published by Ronald D. Bass, MD, MBA, of Georgetown University.
LIMITATIONS:
Study focused on Black vs. non-Black SSc patients, potential selection bias.
Overlapping patients may not represent true overlap of conditions.
DISCLOSURES:
No external funding sources or relevant financial relationships reported.
Stats
Among the 402 patients with SSc analyzed, 10% met the 2019 EULAR/ACR Classification Criteria for SLE.
The prevalence of anti-U1-RNP antibody positivity was 30% in SSc-SLE patients and 6.6% in those with SSc only.
Quotes
"The results highlight the need for clinicians to recognize the SSc-SLE overlap syndrome."
"Patients with both SSc and SLE were significantly more likely to be female and Black."