Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris.


Journal

European journal of human genetics : EJHG
ISSN: 1476-5438
Titre abrégé: Eur J Hum Genet
Pays: England
ID NLM: 9302235

Informations de publication

Date de publication:
16 Mar 2023
Historique:
received: 21 07 2022
accepted: 21 02 2023
revised: 02 02 2023
pubmed: 17 3 2023
medline: 17 3 2023
entrez: 16 3 2023
Statut: aheadofprint

Résumé

Acne vulgaris is a common chronic skin disorder presenting with comedones, cystic structures forming within the distal hair follicle, and in most cases additionally with inflammatory skin lesions on the face and upper torso. We performed a genome-wide association study and meta-analysis of data from 34,422 individuals with acne and 364,991 controls from three independent European-ancestry cohorts. We replicated 19 previously implicated genome-wide significant risk loci and identified four novel loci [11q12.2 (FADS2), 12q21.1 (LGR5), 17q25.3 (FASN), and 22q12.1 (ZNRF3-KREMEN1)], bringing the total number of reported acne risk loci to 50. Our meta-analysis results explain 9.4% of the phenotypic variance of acne. A polygenic model of acne risk variants showed that individuals in the top 5% of the risk percentiles had a 1.62-fold (95% CI 1.47-1.78) increased acne risk relative to individuals with average risk (20-80% on the polygenic risk score distribution). Our findings highlight the Wnt and MAPK pathways as key factors in the genetic predisposition to acne vulgaris, together with the effects of genetic variation on the structure and maintenance of the hair follicle and pilosebaceous unit. Two novel loci, 11q12.2 and 17q25.3, contain genes encoding key enzymes involved in lipid biosynthesis pathways.

Identifiants

pubmed: 36922633
doi: 10.1038/s41431-023-01326-8
pii: 10.1038/s41431-023-01326-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj)
ID : 2014-2020.4.01.15-0012
Organisme : EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj)
ID : 2014-2020.4.01.16012
Organisme : Eesti Teadusagentuur (Estonian Research Council)
ID : PRG1189

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2023. The Author(s).

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Auteurs

Maris Teder-Laving (M)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia. maris.teder-laving@ut.ee.

Mart Kals (M)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.

Anu Reigo (A)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.

Riin Ehin (R)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
Institute of Health Technologies, Tallinn University of Technology, Tallinn, Estonia.
BioCC Ltd, Tartu, Estonia.

Telver Objärtel (T)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.

Mariliis Vaht (M)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.

Tiit Nikopensius (T)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.

Andres Metspalu (A)

Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.

Külli Kingo (K)

Faculty of Medicine, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
Tartu University Hospital, Tartu, Estonia.

Classifications MeSH