Menu
GWAS Study

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci.

Mitchell BL, Saklatvala JR, Dand N et al.

35132056 PubMed ID
GWAS Study Type
615396 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MB
Mitchell BL
SJ
Saklatvala JR
DN
Dand N
HF
Hagenbeek FA
LX
Li X
MJ
Min JL
TL
Thomas L
BM
Bartels M
JH
Jan Hottenga J
LM
Lupton MK
BD
Boomsma DI
DX
Dong X
HK
Hveem K
LM
Løset M
MN
Martin NG
BJ
Barker JN
HJ
Han J
SC
Smith CH
RM
Rentería ME
SM
Simpson MA
Chapter II

Abstract

Summary of the research findings

Acne vulgaris is a highly heritable skin disorder that primarily impacts facial skin. Severely inflamed lesions may leave permanent scars that have been associated with long-term psychosocial consequences. Here, we perform a GWAS meta-analysis comprising 20,165 individuals with acne from nine independent European ancestry cohorts. We identify 29 novel genome-wide significant loci and replicate 14 of the 17 previously identified risk loci, bringing the total number of reported acne risk loci to 46. Using fine-mapping and eQTL colocalisation approaches, we identify putative causal genes at several acne susceptibility loci that have previously been implicated in Mendelian hair and skin disorders, including pustular psoriasis. We identify shared genetic aetiology between acne, hormone levels, hormone-sensitive cancers and psychiatric traits. Finally, we show that a polygenic risk score calculated from our results explains up to 5.6% of the variance in acne liability in an independent cohort.

20,165 European ancestry cases, 595,231 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

615396
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.