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GWAS Study

Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne.

Petridis C, Navarini AA, Dand N et al.

30542056 PubMed ID
GWAS Study Type
26722 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PC
Petridis C
NA
Navarini AA
DN
Dand N
SJ
Saklatvala J
BD
Baudry D
DM
Duckworth M
AM
Allen MH
CC
Curtis CJ
LS
Lee SH
BA
Burden AD
LA
Layton A
BV
Bataille V
PA
Pink AE
CI
Carlavan I
VJ
Voegel JJ
ST
Spector TD
TR
Trembath RC
MJ
McGrath JA
SC
Smith CH
BJ
Barker JN
SM
Simpson MA
Chapter II

Abstract

Summary of the research findings

Acne vulgaris is a highly heritable common, chronic inflammatory disease of the skin for which five genetic risk loci have so far been identified. Here, we perform a genome-wide association study of 3823 cases and 16,144 controls followed by meta-analysis with summary statistics from a previous study, with a total sample size of 26,722. We identify 20 independent association signals at 15 risk loci, 12 of which have not been previously implicated in the disease. Likely causal variants disrupt the coding region of WNT10A and a P63 transcription factor binding site in SEMA4B. Risk alleles at the 1q25 locus are associated with increased expression of LAMC2, in which biallelic loss-of-function mutations cause the blistering skin disease epidermolysis bullosa. These findings indicate that variation affecting the structure and maintenance of the skin, in particular the pilosebaceous unit, is a critical aspect of the genetic predisposition to severe acne.

5,602 European ancestry cases, 21,120 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

26722
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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