Literature DB >> 20331450

Narrowband ultraviolet B treatment improves vitamin D balance and alters antimicrobial peptide expression in skin lesions of psoriasis and atopic dermatitis.

K Vähävihu1, M Ala-Houhala, M Peric, P Karisola, H Kautiainen, T Hasan, E Snellman, H Alenius, J Schauber, T Reunala.   

Abstract

BACKGROUND: Narrowband ultraviolet B (NB-UVB) is a routine treatment for psoriasis and atopic dermatitis (AD) but its effect on vitamin D balance is not well studied.
OBJECTIVES: To examine whether NB-UVB treatment in winter improves vitamin D balance in psoriasis and AD, and to study the effects of NB-UVB on antimicrobial peptide and cytokine expression in the skin.
METHODS: Eighteen adult patients with psoriasis, 18 with AD and 15 healthy subjects received a total of 15 NB-UVB exposures on the whole body, given three times a week. Serum calcidiol (25-hydroxyvitamin D) was measured by radioimmunoassay. Antimicrobial peptide and cytokine expression in skin lesions was examined by real-time quantitative polymerase chain reaction.
RESULTS: At onset 16 (89%) patients with psoriasis, 17 (94%) patients with AD and eight (53%) healthy subjects had vitamin D insufficiency (calcidiol < 50 nmol L(-1)). NB-UVB treatment significantly increased (P < 0.001) serum calcidiol. The increase was 59.9 nmol L(-1) (95% confidence interval, CI 53.5-66.9) in psoriasis, 68.2 nmol L(-1) (95% CI 55.4-80.1) in AD and 90.7 nmol L(-1) (95% CI 63.8-123.4) in healthy subjects. Psoriasis Area and Severity Index and SCORAD improved significantly (P < 0.001) but no correlation to the increase of serum calcidiol was found. Cathelicidin and human beta-defensin 2 (HBD2) expression was high in skin lesions of psoriasis. After six NB-UVB treatments cathelicidin increased further while HBD2 expression decreased. A similar trend was observed in AD lesions. NB-UVB caused a marked but nonsignificant decrease of interleukin (IL)-1beta and IL-17 in psoriasis lesions.
CONCLUSIONS: The present study shows that in addition to a significant improvement of psoriasis and AD, NB-UVB treatment effectively corrects vitamin D insufficiency. It also increases cathelicidin and decreases HBD2 levels in healing skin lesions of psoriasis and AD. This effect might be mediated by improved vitamin D balance and the local cytokine network.

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Year:  2010        PMID: 20331450     DOI: 10.1111/j.1365-2133.2010.09767.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  32 in total

1.  Impact of vitamin D3 on cutaneous immunity and antimicrobial peptide expression.

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Authors:  Keith D Roby; Anna Di Nardo
Journal:  Drug Discov Today Dis Mech       Date:  2013-12-01

7.  Antimicrobial implications of vitamin D.

Authors:  Dima A Youssef; Christopher Wt Miller; Adel M El-Abbassi; Della C Cutchins; Coleman Cutchins; William B Grant; Alan N Peiris
Journal:  Dermatoendocrinol       Date:  2011-10-01

Review 8.  Antimicrobial peptides in the pathogenesis of psoriasis.

Authors:  Shin Morizane; Richard L Gallo
Journal:  J Dermatol       Date:  2012-03       Impact factor: 4.005

9.  A randomized controlled double-blind investigation of the effects of vitamin D dietary supplementation in subjects with atopic dermatitis.

Authors:  T R Hata; D Audish; P Kotol; A Coda; F Kabigting; J Miller; D Alexandrescu; M Boguniewicz; P Taylor; L Aertker; K Kesler; J M Hanifin; D Y M Leung; R L Gallo
Journal:  J Eur Acad Dermatol Venereol       Date:  2013-05-03       Impact factor: 6.166

10.  Pathological role of excessive DNA as a trigger of keratinocyte proliferation in psoriasis.

Authors:  Y Luo; T Hara; A Kawashima; Y Ishido; S Suzuki; N Ishii; T Kambara; K Suzuki
Journal:  Clin Exp Immunol       Date:  2020-06-08       Impact factor: 4.330

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