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Table 1 Characteristic of patients with Behçet’s disease who were enrolled in the study

From: Changes in the proportion of clinical clusters contribute to the phenotypic evolution of Behçet’s disease in Japan

Characteristics

Yokohama City University registry (n = 657)

Japan national registry (n = 6754)

Sex: female/male, n (%)

372/285 (56.6/43.4)

3990/2764 (59.1/40.9)

Age of diagnosis (mean ± SD)

36.58 ± 12.29

36.68 ± 14.23

Observation period (mean ± SD)

13.72 ± 11.79

4.14 ± 7.62

Disease phenotype

 Oral ulcer, n (%)

653 (99.4)

6336 (93.8)

 Skin involvement, n (%)

585 (89.0)

5483 (81.2)

 Eye involvement, n (%)

392 (59.7)

2344 (34.7)

 Genital ulcer, n (%)

474 (72.1)

4242 (62.8)

 Arthritis, n (%)

346 (52.7)

3311 (49.0)

 Epididymitis, n/available data number (%)

15/285 (5.3)

257/2764 (9.3)

 Gastrointestinal involvement, n (%)

113 (17.2)

906 (13.4)

 Vascular involvement, n (%)

55 (8.4)

148 (2.2)

 Neurological involvement, n (%)

67 (10.2)

350 (5.2)

 Pathergy test, n/available data number (%)

74/170 (43.5)

1361/4225 (32.2)

Other characteristics

 HLA-B51, n/available data number (%)

214/449 (47.7)

1389/3141 (44.2)

 Fulfilling ISG criteria, n (%)

583 (88.7)

4980 (73.7)

 Fulfilling ITR-ICBD criteria, n (%)

645 (98.2)

5586 (82.7)

 Smoking, n/available data number (%)

233/455 (51.2)

N/A

 Hospitalization, n/available data number (%)

239/522 (45.8)

1556/6002 (25.9)

 Blindness, n/available data number (%)

98/582 (16.8)

N/A

 Death caused by BD, n/available data number (%)

3/520 (0.6)

N/A

Treatments

 Colchicine, n (%)

375/522 (71.8)

2942 (43.6)

 Glucocorticoid, n (%)

236/522 (45.2)

2352 (34.8)

 Maximum Prednisolone dose (mg/day, mean ± SD)

11.75 ± 17.76

N/A

 Methylprednisolone pulse therapy, n/available data number (%)

36/522 (6.9)

N/A

 Immunosuppressant therapy, n/available data number (%)

203/522 (38.9)

578 (8.6)

 Biologics, n (%)

95 (14.5)

N/A

  Infliximab, n (%)

86 (13.1)

N/A

  Adalimumab, n (%)

24 (3.7)

N/A

  Others, n (%)*

3 (0.5)

N/A

 Time from diagnosis to biologics (years, mean ± SD)

6.22 ± 8.52

N/A

  1. BDRC Behçet’s Disease Research Committee, ISG International Study Group, ITR-ICBD International Team for the Revision of the International Criteria for Behçet’s Disease, N/A not available
  2. *Others: etanercept 2, tocilizumab 1