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. 2024 Feb 15;63(11):2981–2988. doi: 10.1093/rheumatology/keae110

Table 1.

Participant characteristics

Variable SSc (n = 407) SSc-ILD (n = 252) SSc No-ILD (n = 155) P-value
Age at biomarker collection 58.81 (50.51–66.40) 58.67 (50.56–66.69) 59.24 (49.46–65.51) 0.719
Disease duration, years 8.29  (3.38–16.98) 6.83 (2.52–15.63) 7.65 (2.43–15.58) 0.742
Follow-up period, years 6.31 (3.11–9.22) 6.50 (2.85–9.16) 6.09 (3.56–9.45) 0.699
Sex, n (%) Male 80 (19.7) 50 (19.8) 30 (19.4) 0.905
Female 327 (80.3) 202 (80.2) 125 (80.6)
Caucasian, n (%) No 45 (11.1) 37 (14.7) 8 (5.2) 0.003
Yes 361 (88.9) 215 (85.3) 146 (94.8)
Disease subtype, n (%) Limited 272 (66.8) 152 (60.3) 120 (77.4) <0.001
Diffuse 135 (33.2) 100 (39.7) 35 (22.6)
Antibody profile, n (%) ANA positive 386 (94.8) 242 (96.0) 144 (92.9) 0.166
Centromere 124 (30.7) 49 (19.6) 75 (48.7) <0.001
Scl-70 105 (26.1) 89 (35.6) 16 (10.5) <0.001
RNA Polymerase III 49 (15.2) 31 (15.3) 18 (15.1) 0.972
FVC% 92.4 (22.60) 87.5 (21.88) 100.4 (21.5) <0.001
PAH, n (%) 70 (17.2) 42 (16.7) 28 (18.1) 0.717
Died during follow-up, n (%) 120 (29.5) 85 (33.7) 35 (22.6) 0.017
FVC% drop >10% during follow-up, n (%) 281 (72.6) 178 (75.4)

Bold typeface used for statistically significant results (P ≤ 0.05).

SSc-ILD: SSc-associated interstitial lung disease; FVC%: forced vital capacity percentage predicted; PAH: pulmonary arterial hypertension.