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. 2024 Jul 1;14(3):e2024179. doi: 10.5826/dpc.1403a179

Table 1.

Selected baseline demographic and clinical characteristic of the sample, overall and by type of anti-IL23.

Variables Overall sample (n=427) Guselkumab (n=201) Risankizumab (n=116) Tildrakizumab (n=110) p*
Mean age in years (SD) 54.3 (14.7) 52.8 (14.6) 56.0 (13.6) 55.2 (15.7)
Male gender, % 63.2 60.7 62.9 68.2
Mean BMI (SD) 27.9 (5.2) 27.8 (5.4) 27.9 (5.0) 28.2 (5.0)
Current smoker, % 58.4 49.4 68.5 63.6 a, b
Comorbidities, %
 None 36.1 36.3 31.9 40.0
 One 43.3 38.8 50.9 43.6 a
 Two 17.3 19.4 15.5 15.5
 Three or more 3.3 5.5 1.7 0.9 b, c
Mean length of disease in years (SD) 20.6 (12.4) 20.1 (12.5) 21.7 (12.2) 20.2 (12.6)
Mean age at onset (SD) 33.3 (16.0) 32.3 (16.2) 33.7 (14.4) 34.8 (17.2)
Concomitant arthritis, % 27.3 30.8 28.7 19.3 b
Psoriasis type, %
 Vulgaris 84.0 84.6 80.9 86.4
 Inverse 3.1 2.5 0.8 6.4 a, b, c
 OthersA 4.9 3.4 7.0 5.4
 CompositeB 8.0 9.5 11.3 1.8 b
Psoriasis site, %
 Typical 58.8 58.7 44.8 73.6 a, b, c
 Folds 27.2 28.8 35.3 15.5 b, c
 Hands and feet 11.7 10.0 16.4 10.0
 Others (nails, scalp, genital) 2.3 2.5 3.5 0.9
Number of previous traditional treatments, %
 None 4.2 4.0 1.7 7.3
 One 31.6 28.9 29.3 39.1
 Two 34.2 33.3 33.6 36.4
 Three or more 30.0 33.8 35.3 17.3
Number of previous biologic treatments, % (N=395) (N=189) (N=111) (N=95)
 None 24.8 23.8 26.1 25.3
 One 29.9 23.3 24.3 49.5
 Two 21.3 22.2 25.2 14.7 b
 Three or more 24.0 30.7 24.3 10.5 b
Median duration of previous biologic treatments in months (IQR) 29.0 (69.5) 35.0 (69.0) 40.0 (60.0) 14.5 (24.0)
Mean PASI at baseline (SD) 12.9 (7.3) 13.5 (7.6) 11.9 (7.1) 12.9 (6.8)

SD: Standard deviation; IQR: Interquartile range. PASI: Psoriasis area severity index.

A

Guttate, pustular, or erythrodermic psoriasis;

B

More than one type of psoriasis concomitantly reported.

*

Chi-squared test for categorical variables; one-way ANOVA with Sidak corrections for continuous ones.

a: p<0.05 for the comparison between patients treated with Guselkumab and patients treated with Risankizumab; b: p<0.05 for the comparison between patients treated with Guselkumab and patients treated with Tildrakizumab; c: p<0.05 for the comparison between patients treated with Risankizumab and patients treated with Tildrakizumab. All p-values that are not indicated were ≥0.05.