Abstract
A course of treatment with narrow-band ultraviolet B (NB-UVB) improves psoriasis and increases serum 25-hydroxyvitamin D (25(OH)D). In this study 12 patients with psoriasis who were supplemented with oral cholecalciferol, 20 µg daily, were given a course of NB-UVB and their response measured. At baseline, serum 25(OH)D was 74.14 ± 22.9 nmol/l. At the 9th exposure to NB-UVB 25(OH)D had increased by 13.2 nmol/l (95% confidence interval (95% CI) 7.2–18.4) and at the 18th exposure by 49.4 nmol/l (95% CI 35.9–64.6) above baseline. Psoriasis Area Severity Index score improved from 8.7 ± 3.5 to 4.5 ± 2.0 (p < 0.001). At baseline, psoriasis lesions showed low vitamin D metabolizing enzyme (CYP27A1, CYP27B1) and high human β-defensin-2 mRNA expression levels compared with those of the healthy subjects. In conclusion, NB-UVB treatment significantly increases serum 25(OH)D in patients with psoriasis who are taking oral vitamin D supplementation, and the concentrations remain far from the toxicity level. Healing psoriasis lesions show similar mRNA expression of vitamin D metabolizing enzymes, but higher antimicrobial peptide levels than NB-UVB-treated skin in healthy subjects.
Original language | English |
---|---|
Pages (from-to) | 146-151 |
Number of pages | 6 |
Journal | Acta Dermato-Venereologica |
Volume | 94 |
Issue number | 2 |
Early online date | 27 Aug 2013 |
DOIs | |
Publication status | Published - Mar 2014 |
Keywords
- 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
- Administration, Oral
- Adult
- Biopsy
- Cholecalciferol
- Cholestanetriol 26-Monooxygenase
- Female
- Humans
- Male
- Middle Aged
- Psoriasis
- RNA, Messenger
- Real-Time Polymerase Chain Reaction
- Skin
- Ultraviolet Therapy
- Vitamin D
- Vitamin D Deficiency
- Vitamins
- beta-Defensins