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. 2023 May 16;24(10):8817. doi: 10.3390/ijms24108817

Table 2.

Variations in IL-36α levels within the BS cohort, according to manifestations in the whole medical history, presence of HLA-B51, active disease at time of enrolment and pharmacological therapies.

With the Considered
Feature
Without the Considered
Feature
p-Value #
IL-36 (pg/mL) IL-36 (pg/mL)
Overall 201.7 (112.7–320.2)
Disease manifestations
Genital aphthosis 269.4 (173.2–384.5) 176.1 (109.2–266.3) 0.015 *
Cutaneous 207.2 (132.9–323.4) 192.2 (94.9–271.2) 0.284
Arthritis 201.7 (120.2–320.2) 194.2 (104.8–344.2) 0.784
Intestinal symptoms 212.2 (104.8–360.4) 200.2 (118.2–316.5) 0.950
Uveitis 243.4 (192.2–345.1) 173.2 (94.9–312.3) 0.029 *
Vascular 269.4 (208.2–351.4) 192.2 (108.1–296.2) 0.072
Neurological 228.3 (171.1–375.2) 194.3 (108.1–318.3) 0.240
HLA-B51 229.7 (152.0–340.8) 193.2 (94.9–312.3) 0.237
Active disease 200.7 (106.5–379.9) 201.7 (133.0–296.2) 0.529
BDCAF Spearman’s rho: 0.492 <0.001 *
Ongoing immunomodulating treatment
Corticosteroids/colchicine 245.7 (160.5–348.3) 0.138
csDMARDs 192.2 (120.2–252.2)
Biologic (±cs) DMARDs 176.1 (82.9–294.4)

# p-value from Mann-Whitney or Krusal–Wallis test for unpaired data, comparing IL-36α levels in patients with vs without a considered feature. * Statistically significant with p-value < 0.05. BDCAF: Behçet’s Disease Current Activity Form; csDMARD: conventional synthetic disease-modifying antirheumatic drugs; HLA: human leukocyte antigen.