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. 2020 Sep 23;11:574992. doi: 10.3389/fimmu.2020.574992

Table 2.

Univariate analysis of initial diagnosis in HA20 patients based on types of A20 disruption.

Initial diagnosis of HA20 Total (n = 89) OTU+ZnF (n = 50) OTU (n = 13) ZnF (n = 26) Fisher P-value
BD 43% (38/89) 48% (24/50) 77% (10/13) 15% (4/26) 15.044 0.001
0.116a
0.006b
<0.001c
iBD 26% (23/89) 28% (14/50) 46% (6/13) 12% (3/26) 5.654 0.068
JIA 12% (11/89) 16% (8/50) 0% (0/13) 12% (3/26) 2.052 0.362
PFAPA 7% (6/89) 4% (2/50) 0% (0/13) 15% (4/26) 3.526 0.172
CD 6% (5/89) 4% (2/50) 0% (0/13) 12% (3/26) 2.087 0.418
RA 4% (4/89) 6% (3/50) 0% (0/13) 4% (1/26) 0.508 1.000
SLE 4% (4/89) 6% (3/50) 0% (0/13) 4% (1/26) 0.508 1.000
PsA 2% (2/89) 2% (1/50) 0% (0/13) 4% (1/26) 0.920 1.000
a

Comparison of the initial diagnosis between OTU+ZnF and OTU groups;

b

Comparison of the initial diagnosis between OTU+ZnF and ZnF groups;

c

Comparison of the initial diagnosis between OTU and ZnF groups. BD, Behcet's disease; iBD, intestinal Behcet's disease; JIA, juvenile idiopathic arthritis; PFAPA, periodic fever with aphthous pharyngitis and adenitis; CD, Crohn's disease; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; PsA, psoriatic arthritis.