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. 2023 Apr 7;9(2):e002971. doi: 10.1136/rmdopen-2022-002971

Table 1.

Characteristics of SSc patients categorised on cohort-entry year

2010–2013
N=229
2014–2017
N=207
2018–2021
N=207
P value
Age, mean (SD) 53 (15) 57 (14) 55 (14) 0.004
Female 195 (85) 157 (76) 157 (76) 0.021
RP duration, months, median (IQR) 120 (44–240) 93 (20–202) 68 (21–210) 0.010
Non-RP duration, months, median (IQR) 46 (16–127) 20 (5–112) 17 (6–55) <0.001
Time since diagnosis, months, median (IQR) 22 (5–99) 9 (1–51) 4 (0–18) <0.001
Fulfilling ARA 1980 criteria for SSc 181 (79) 152 (73) 155 (75) 0.360
Anticentromere antibodies 88 (38) 87 (42) 100 (49) 0.091
Antitopoisomerase antibodies 53 (23) 49 (24) 36 (18) 0.248
Disease subset: 0.160
 Non-cutaneous 43 (19) 50 (24) 43 (21)
 Limited cutaneous 144 (62) 109 (53) 130 (63)
 Diffuse cutaneous 42 (18) 48 (23) 34 (16)
Pulmonary arterial hypertension 8 (4) 5 (2) 6 (3) 0.801
Cardiac involvement 11 (5) 12 (6) 25 (12) 0.008
Interstitial lung disease on HRCT 99 (43) 65 (31) 64 (31) 0.033
Interstitial lung disease on HRCT and FVC <80% 27 (12) 20 (10) 12 (6) 0.092
Gastrointestinal involvement 56 (25) 55 (27) 46 (22) 0.588
Renal crisis 5 (2) 3 (1) 5 (3) 0.570
Musculoskeletal involvement 40 (18) 42 (20) 28 (14) 0.185
Digital ulcers 45 (20) 26 (13) 23 (12) 0.036

All binary variables are presented as numbers with percentages.

ARA, American Rheumatism Association; FVC, forced vital capacity; HRCT, high-resolution CT; ILD, interstitial lung disease; N, number; RP, Raynaud’s phenomenon; SSc, systemic sclerosis.