| Literature DB >> 25705849 |
Leonie C Jacobs1, Merel A Hamer1, David A Gunn2, Joris Deelen3, Jaspal S Lall2, Diana van Heemst4, Hae-Won Uh5, Albert Hofman6, André G Uitterlinden7, Christopher E M Griffiths8, Marian Beekman3, P Eline Slagboom3, Manfred Kayser9, Fan Liu9, Tamar Nijsten10.
Abstract
Facial pigmented spots are a common skin aging feature, but genetic predisposition has yet to be thoroughly investigated. We conducted a genome-wide association study for pigmented spots in 2,844 Dutch Europeans from the Rotterdam Study (mean age: 66.9±8.0 years; 47% male). Using semi-automated image analysis of high-resolution digital facial photographs, facial pigmented spots were quantified as the percentage of affected skin area (mean women: 2.0% ±0.9, men: 0.9% ±0.6). We identified genome-wide significant association with pigmented spots at three genetic loci: IRF4 (rs12203592, P=1.8 × 10(-27)), MC1R (compound heterozygosity score, P=2.3 × 10(-24)), and RALY/ASIP (rs6059655, P=1.9 × 10(-9)). In addition, after adjustment for the other three top-associated loci the BNC2 locus demonstrated significant association (rs62543565, P=2.3 × 10(-8)). The association signals observed at all four loci were successfully replicated (P<0.05) in an independent Dutch cohort (Leiden Longevity Study n=599). Although the four genes have previously been associated with skin color variation and skin cancer risk, all association signals remained highly significant (P<2 × 10(-8)) when conditioning the association analyses on skin color. We conclude that genetic variations in IRF4, MC1R, RALY/ASIP, and BNC2 contribute to the acquired amount of facial pigmented spots during aging, through pathways independent of the basal melanin production.Entities:
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Year: 2015 PMID: 25705849 DOI: 10.1038/jid.2015.62
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551