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. 2025 Aug 21;55(4):207–214. doi: 10.4274/tjo.galenos.2025.67513

Table 1. Baseline demographic and clinical features .

Number of patients/eyes, N/n

146/289

Age, mean ± SD (range), years

 <18 years, N (%)

         >60 years, N (%)

37.6 ± 14.4 (4-73)

8 (5.5)*

6 (4.1)**

Sex, N (%)

Female

        Male

-

60 (41.1)

86 (58.9)

Localization of uveitis, N (%)

Anterior uveitis

        Intermediate uveitis

        Posterior uveitis

        Panuveitis

-

17 (11.6)

8 (5.5)

26 (17.8)

95 (65.1)

Uveitis etiology, N (%)

Behçet’s uveitis

        Sarcoidosis

        Vogt-Koyanagi-Harada disease

        Spondyloarthropathy-associated uveitis

        Serpiginous choroiditis

        Pars planitis

        Juvenile idiopathic arthritis-associated uveitis

        Ampiginous choroiditis

        Idiopathic uveitis

        Tubulointerstitial nephritis and uveitis syndrome

        Sympathetic ophthalmia

        Tuberculosis-related uveitis

        Posterior scleritis***

-

53 (36.3)

28 (19.2)

18 (12.3)

12 (8.2)

7 (4.8)

6 (4.1)

5 (3.4)

4 (2.7)

4 (2.7)

3 (2.1)

3 (2.1)

2 (1.4)

1 (0.7)

Previous systemic steroid, N (%)

 None

        <10 mg/day

        16 mg/day

        32 mg/day

        48 mg/day

        64 mg/day

-

109 (74.7)

12 (8.3)

5 (3.4)

9 (6.2)

2 (1.4)

9 (6.2)

Previous IST/immunomodulatory/biologics****, N (%)

None

        Azathioprine

        Methotrexate

        Mycophenolate mofetil

        Cyclosporine

        Etanercept

        Certolizumab

        Interferon-α

-

12 (8.2)

57 (39.1)

37 (25.3)

1 (0.7)

51 (34.9)

6 (4.1)

1 (0.7)

18 (12.3)

Line of ADA, N (%)

    First-line therapy

        Second-line therapy

-

12 (8.2)

134 (91.8)

Interval between diagnosis and initiation of ADA treatment, median (IQR), months

13.5 (7-36)

Duration of ADA treatment; median (IQR), months

12 (9-24)

N, Number of patients, n: Number of eyes, SD: Standard deviation, IST: Immunosuppressive treatment, ADA: Adalimumab, IQR: Interquartile range

*Patients started on ADA before the age of 18 years were diagnosed with juvenile idiopathic arthritis-associated uveitis (4 patients), tubulointerstitial nephritis and uveitis syndrome (2 patients), pars planitis (1 patient), and sympathetic ophthalmia (1 patient)

**Among patients over 60 years of age, ADA was initiated in one patient due to Vogt-Koyanagi-Harada and in the remaining five patients due to ocular sarcoidosis

***Posterior scleritis is included under posterior uveitis in the uveitis localization section.

****Some patients received combined ISTs