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Assessment of the Genetic Basis of Rosacea by Genome-Wide Association Study.

J Invest Dermatol. 2015 Feb 19;

Authors: Chang AL, Raber I, Xu J, Li R, Spitale R, Chen J, Kiefer AK, Tian C, Eriksson NK, Hinds DA, Tung J

Abstract
Rosacea is a common, chronic skin disease that is currently incurable. Although environmental factors influence rosacea, the genetic basis of rosacea is not established. In this genome-wide association study, a discovery group of 22,952 individuals (2,618 rosacea cases and 20,334 controls) was analyzed, leading to identification of two significant single nucleotide polymorphisms (SNPs) associated with rosacea, one of which replicated in a new group of 29,481 individuals (3,205 rosacea cases and 26,262 controls). The confirmed SNP, rs763035 (p=8.0 × 10(-11) discovery group; p=0.00031 replication group), is inter-genic between HLA-DRA and BTNL2. Exploratory immunohistochemical analysis of HLA-DRA and BTNL2 expression in papulopustular rosacea lesions from six individuals, including one with the rs763035 variant, revealed staining in the peri-follicular inflammatory infiltrate of rosacea for both proteins. In addition, three HLA alleles, all MHC class II proteins, were significantly associated with rosacea in the discovery group and confirmed in the replication group: HLA-DRB1*03:01 (p=1.0 × 10(-8) discovery group; p=4.4 × 10(-6) replication group), HLA-DQB1*02:01 (p=1.3 × 10(-8) discovery group; p=7.2 × 10(-6) replication group), and HLA-DQA1*05:01 (p=1.4 × 10(-8) discovery group; p=7.6 × 10(-6) replication group). Collectively, the gene variants identified in this study support the concept of a genetic component for rosacea, and provide candidate targets for future studies to better understand and treat rosacea.Journal of Investigative Dermatology accepted article preview online, 19 February 2015. doi:10.1038/jid.2015.53.

PMID: 25695682 [PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/25695682?dopt=Abstract = URL to article

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