Title
Genome-wide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2 Genome-wide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
Author
Faculty/Department
Faculty of Medicine and Health Sciences
Publication type
article
Publication
Copenhagen ,
Subject
Human medicine
Source (journal)
Experimental dermatology. - Copenhagen
Volume/pages
(2016) , p. 1-18
ISSN
0906-6705
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Affiliation
University of Antwerp
Abstract
Alopecia areata (AA) is a common hair loss disorder of autoimmune etiology, which often results in pronounced psychological distress. Understanding of the pathophysiology of AA is increasing, due in part to recent genetic findings implicating common variants at several genetic loci. To date, no study has investigated the contribution of copy number variants (CNVs) to AA, a prominent class of genomic variants involved in other autoimmune disorders. Here, we report a genome-wide- and a candidate gene focused CNV analysis performed in a cohort of 585 AA patients and 1,340 controls of Central European origin. A nominally significant association with AA was found for CNVs in the following five chromosomal regions: 4q35.2, 6q16.3, 9p23, 16p12.1, and 20p12.1. The most promising finding was a 342.5 kb associated region in 6q16.3 (duplications in 4/585 patients; 0/1,340 controls). The duplications spanned the genes MCHR2 and MCHR2-AS1, implicated in melanin-concentrating hormone (MCH) signaling. These genes have not been implicated in previous studies of AA pathogenesis. However, previous research has shown that MCHR2 affects the scale color of barfin flounder fish via the induction of melanin aggregation. AA preferentially affects pigmented hairs, and the hair of AA patients frequently shows a change in color when it regrows following an acute episode of AA. This might indicate a relationship between AA, pigmentation, and MCH signaling. In conclusion, the present results provide suggestive evidence for the involvement of duplications in MCHR2 in AA pathogenesis.
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