Table 1

Distribution of ILD in anti-Ro52 positive patients with various underlying diseases

TotalRo52+Ro60Ro52+Ro60+OR95% ClP value
CTD*490 (37.1%)352 (55.4%)138 (20.1%)4.943.88 to 6.31<0.0001
 IIM ‡123 (85.4%)99 (88.4%)24 (75.0%)2.540.93 to 6.77>0.05
DM84 (87.5%)66 (86.8%)18 (90.0%)0.730.15 to 3.22>0.05
PM18 (66.7%)15 (83.3%)3 (33.3%)10.001.42 to 48.96<0.01
ASS21 (100.0%)18 (100.0%)3 (100.0%)
 pSS236 (38.2%)157 (57.3%)79 (23.0%)4.503.17 to 6.31<0.0001
 SLE18 (6.5%)4 (7.4%)14 (6.3%)1.180.41 to 3.64>0.05
 RA36 (43.4%)29 (60.4%)7 (20.0%)6.112.12 to 15.16<0.001
 SSc15 (51.7%)11 (57.9%)4 (40.0%)2.060.44 to 8.04>0.05
 UCTD49 (64.5%)44 (69.8%)5 (38.5%)3.711.16 to 11.61<0.05
 MCTD/overlap syndrome7 (46.7%)3 (30.0%)4 (80.0%)0.110.01 to 1.50>0.05
 Vasculitis6 (35.3%)5 (38.5%)1 (25.0%)1.880.21 to 28.67>0.05
Non-CTD†72 (10.9%)68 (12.2%)4 (3.9%)3.411.25 to 8.95<0.05
  • Data were shown as number (percentage of ILD patients for each disease). Ro52+Ro60: anti-Ro52 positive and anti-Ro60 negative, Ro52+Ro60+: both anti-Ro52 and anti-Ro60 positive.

  • *Diagnosis of CTDs was in accordance with the international criteria for classification.

  • †Patients without a definite CTD during the hospitalisation, of which tumour, infection, ILD and chronic kidney disease were the most common disease types.

  • ‡including DM, PM and ASS.

  • ASS, anti-synthetase syndrome; CTD, connective tissue disease; DM, dermatomyositis; IIM, idiopathic inflammatory myopathy; MCTD, mixed connective tissue disease; PM, polymyositis; pSS, primary Sjögren's syndrome; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; SSc, systemic sclerosis; UCTD, undifferentiated connective tissue disease.