In diffuse systemic sclerosis, the antibody most associated with pulmonary fibrosis and worst prognosis is:
- A Anti-topoisomerase I (anti-Scl-70) ✓
- B Anti-centromere antibody (ACA)
- C Anti-RNA polymerase III antibody
- D Anti-U1 RNP antibody
Explanation
Anti-topoisomerase I (anti-Scl-70) antibodies are found in 30–40% of diffuse systemic sclerosis patients and are associated with diffuse skin thickening, pulmonary interstitial fibrosis, and overall worse prognosis. Anti-centromere antibodies (ACA) are associated with limited SSc/CREST syndrome and pulmonary arterial hypertension (better prognosis overall). Anti-RNA polymerase III is associated with diffuse skin disease and renal crisis. Anti-U1 RNP is associated with mixed connective tissue disease.
Reference: Neena Khanna Illustrated Synopsis of Dermatology & STD, 6th ed.
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Written and medically reviewed by the StethoPrep medical team.