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Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02.

Tziotzios C, Petridis C, Dand N et al.

30850646 PubMed ID
GWAS Study Type
5161 Participants
161 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TC
Tziotzios C
PC
Petridis C
DN
Dand N
AC
Ainali C
SJ
Saklatvala JR
PV
Pullabhatla V
OA
Onoufriadis A
PR
Pramanik R
BD
Baudry D
LS
Lee SH
WK
Wood K
LL
Liu L
SS
Seegobin S
MG
Michelotti GA
LS
Lwin SM
CE
Christou EAA
CC
Curtis CJ
DR
de Rinaldis E
SA
Saxena A
HS
Holmes S
HM
Harries M
PI
Palamaras I
CF
Cunningham F
PG
Parkins G
KM
Kaur M
FP
Farrant P
MA
McDonagh A
MA
Messenger A
JJ
Jones J
JV
Jolliffe V
AI
Ali I
AM
Ardern-Jones M
MC
Mitchell C
BN
Burrows N
AR
Atkar R
BC
Banfield C
AA
Alexandroff A
CC
Champagne C
CH
Cooper HL
VS
Vañó-Galván S
MA
Molina-Ruiz AM
PN
Perez NO
PG
Patel GK
MA
Macbeth A
PM
Page M
BA
Bryden A
MM
Mowbray M
WS
Wahie S
AK
Armstrong K
CN
Cooke N
GM
Goodfield M
MI
Man I
DB
de Berker D
DG
Dunnill G
TA
Takwale A
RA
Rao A
ST
Siah TW
SR
Sinclair R
WM
Wade MS
DN
Dlova NC
SJ
Setterfield J
LF
Lewis F
BK
Bhargava K
KN
Kirkpatrick N
EX
Estivill X
SC
Stefanato CM
FC
Flohr C
ST
Spector T
WF
Watt FM
SC
Smith CH
BJ
Barker JN
FD
Fenton DA
SM
Simpson MA
MJ
McGrath JA
Chapter II

Abstract

Summary of the research findings

Frontal fibrosing alopecia (FFA) is a recently described inflammatory and scarring type of hair loss affecting almost exclusively women. Despite a dramatic recent increase in incidence the aetiopathogenesis of FFA remains unknown. We undertake genome-wide association studies in females from a UK cohort, comprising 844 cases and 3,760 controls, a Spanish cohort of 172 cases and 385 controls, and perform statistical meta-analysis. We observe genome-wide significant association with FFA at four genomic loci: 2p22.2, 6p21.1, 8q24.22 and 15q2.1. Within the 6p21.1 locus, fine-mapping indicates that the association is driven by the HLA-B*07:02 allele. At 2p22.1, we implicate a putative causal missense variant in CYP1B1, encoding the homonymous xenobiotic- and hormone-processing enzyme. Transcriptomic analysis of affected scalp tissue highlights overrepresentation of transcripts encoding components of innate and adaptive immune response pathways. These findings provide insight into disease pathogenesis and characterise FFA as a genetically predisposed immuno-inflammatory disorder driven by HLA-B*07:02.

1,016 European ancestry cases, 4,145 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

5161
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K., Spain
Recruitment Country
Chapter IV

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