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GWAS Study

A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis.

Carmona FD, Vaglio A, Mackie SL et al.

28041642 PubMed ID
GWAS Study Type
11259 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CF
Carmona FD
VA
Vaglio A
MS
Mackie SL
HJ
Hernández-Rodríguez J
MP
Monach PA
CS
Castañeda S
SR
Solans R
MI
Morado IC
NJ
Narváez J
RM
Ramentol-Sintas M
PC
Pease CT
DB
Dasgupta B
WR
Watts R
KN
Khalidi N
LC
Langford CA
YS
Ytterberg S
BL
Boiardi L
BL
Beretta L
GM
Govoni M
EG
Emmi G
BF
Bonatti F
CM
Cimmino MA
WT
Witte T
NT
Neumann T
HJ
Holle J
SV
Schönau V
SL
Sailler L
PT
Papo T
HJ
Haroche J
MA
Mahr A
ML
Mouthon L
Molberg Ø
DA
Diamantopoulos AP
VA
Voskuyl A
BE
Brouwer E
DT
Daikeler T
BC
Berger CT
ME
Molloy ES
OL
O'Neill L
BD
Blockmans D
LB
Lie BA
MP
Mclaren P
VT
Vyse TJ
WC
Wijmenga C
AY
Allanore Y
KB
Koeleman BPC
BJ
Barrett JH
CM
Cid MC
SC
Salvarani C
MP
Merkel PA
MA
Morgan AW
GM
González-Gay MA
MJ
Martín J
Chapter II

Abstract

Summary of the research findings

Giant cell arteritis (GCA) is the most common form of vasculitis in individuals older than 50 years in Western countries. To shed light onto the genetic background influencing susceptibility for GCA, we performed a genome-wide association screening in a well-powered study cohort. After imputation, 1,844,133 genetic variants were analyzed in 2,134 case subjects and 9,125 unaffected individuals from ten independent populations of European ancestry. Our data confirmed HLA class II as the strongest associated region (independent signals: rs9268905, p = 1.94 × 10-54, per-allele OR = 1.79; and rs9275592, p = 1.14 × 10-40, OR = 2.08). Additionally, PLG and P4HA2 were identified as GCA risk genes at the genome-wide level of significance (rs4252134, p = 1.23 × 10-10, OR = 1.28; and rs128738, p = 4.60 × 10-9, OR = 1.32, respectively). Interestingly, we observed that the association peaks overlapped with different regulatory elements related to cell types and tissues involved in the pathophysiology of GCA. PLG and P4HA2 are involved in vascular remodelling and angiogenesis, suggesting a high relevance of these processes for the pathogenic mechanisms underlying this type of vasculitis.

2,134 European ancestry cases, 9,125 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

11259
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., Italy, Netherlands, Canada, Germany, U.K., Switzerland, Spain, France, Republic of Ireland, Norway
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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