Journal
BRITISH JOURNAL OF DERMATOLOGY
Volume 171, Issue 6, Pages 1517-1520Publisher
WILEY-BLACKWELL
DOI: 10.1111/bjd.13178
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Funding
- Ingrid Asp foundation
- Welander Foundation
- Swedish Psoriasis Association
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Background NACHT, LRR and PYD domain-containing protein (NLRP) 1 is part of the inflammasome multiprotein complex involved in the production of interleukin (IL)-1 beta and IL-18, two cytokines strongly implicated in psoriasis pathogenesis. Genetic variations in NLRP1 are associated with a predisposition for chronic inflammatory conditions. Objectives The aim of the study was to investigate the role of genetic variation in the NLRP1 inflammasome in psoriasis susceptibility. Material and methods Four haplotype-tagging single-nucleotide polymorphisms (SNPs) (rs6502867, rs8079034, rs878329 and rs12150220) were investigated by TaqMan allelic discrimination in a patient sample comprising 1847 individuals from 478 families and 802 healthy controls. Results Using the transmission disequilibrium test, a significant increase in the transmission of the NLRP1 rs8079034C and rs878329C alleles to patients with psoriasis was demonstrated (P = 0.006 and P = 0.033, respectively). Furthermore, homozygosity for the rs878329C allele correlated with a younger age of onset. We also observed an increase in the expression of NLRP1 mRNA in the peripheral blood cells of patients with psoriasis. This was accompanied by a higher level of circulating IL-18 and appeared to be associated with the rs878329C allele. Conclusions Our data support the involvement of NLRP1 and the NLRP1 inflammasome in psoriasis susceptibility and further support the role of innate immunity in psoriasis.
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