Table 1 |
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|
Patient characteristics |
|
|
Characteristics |
N = 20 |
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|
|
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Epidemiology |
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Age, y, mean ± SD |
31 ± 8 |
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Female gender, n (%) |
20 (100) |
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Previous SLE manifestations |
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|
Skin, n (%) |
11 (55) |
|
Joints, n (%) |
9 (45) |
|
Serositis, n (%) |
4 (20) |
|
Kidney, n (%) |
11 (55) |
|
Central nervous system, n (%) |
1 (5) |
|
SELENA-SLEDAI at Day 0, mean (range) |
2 (0 to 8) |
|
25-Hydroxyvitamin D levels |
|
|
Mean ± SD, ng/mL |
22 ± 11 |
|
25(OH)D ≤ 10 ng/mL, n (%) |
1 (5) |
|
11 < 25(OH)D ≤ 20 ng/mL, n (%) |
11 (55) |
|
21 < 25(OH)D ≤ 30 ng/mL, n (%) |
8 (40) |
|
Associated treatments* |
|
|
Prednisone, n (%) |
14 (70) |
|
Prednisone, median, mg/day (range) |
5 (0 to 15) |
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Hydroxychloroquine, n (%) |
17 (85) |
|
Azathioprine, n (%) |
2 (10) |
|
Mycophenolate mofetil, n (%) |
1 (5) |
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|
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*At the time of the study. SLE: systemic lupus erythematosus; SELENA-SLEDAI: Safety of Estrogens in Lupus Erythematosus National Assessment-Systemic Lupus Erythematosus Disease Activity Index; 25(OH)D: 25-hydroxyvitamin D. |
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Terrier et al. Arthritis Research & Therapy 2012 14:R221 doi:10.1186/ar4060 |
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