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GWAS Study

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target.

Roychowdhury T, Klarin D, Levin MG et al.

37845353 PubMed ID
GWAS Study Type
1125328 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RT
Roychowdhury T
KD
Klarin D
LM
Levin MG
SJ
Spin JM
RY
Rhee YH
DA
Deng A
HC
Headley CA
TN
Tsao NL
GC
Gellatly C
ZV
Zuber V
SF
Shen F
HW
Hornsby WE
LI
Laursen IH
VS
Verma SS
LA
Locke AE
EG
Einarsson G
TG
Thorleifsson G
GS
Graham SE
DO
Dikilitas O
PJ
Pattee JW
JR
Judy RL
PF
Pauls-Verges F
NJ
Nielsen JB
WB
Wolford BN
BB
Brumpton BM
DJ
Dilmé J
PO
Peypoch O
JL
Juscafresa LC
ET
Edwards TL
LD
Li D
BK
Banasik K
BS
Brunak S
JR
Jacobsen RL
GM
Garcia-Barrio MT
ZJ
Zhang J
RL
Rasmussen LM
LR
Lee R
HA
Handa A
WA
Wanhainen A
MK
Mani K
LJ
Lindholt JS
OL
Obel LM
SE
Strauss E
OG
Oszkinis G
NC
Nelson CP
SK
Saxby KL
VH
van Herwaarden JA
VD
van der Laan SW
VS
van Setten J
CM
Camacho M
DF
Davis FM
WR
Wasikowski R
TL
Tsoi LC
GJ
Gudjonsson JE
EJ
Eliason JL
CD
Coleman DM
HP
Henke PK
GS
Ganesh SK
CY
Chen YE
GW
Guan W
PJ
Pankow JS
PN
Pankratz N
PO
Pedersen OB
EC
Erikstrup C
TW
Tang W
HK
Hveem K
GD
Gudbjartsson D
GS
Gretarsdottir S
TU
Thorsteinsdottir U
HH
Holm H
SK
Stefansson K
FM
Ferreira MA
BA
Baras A
KI
Kullo IJ
RM
Ritchie MD
CA
Christensen AH
IK
Iversen KK
EN
Eldrup N
SH
Sillesen H
OS
Ostrowski SR
BH
Bundgaard H
UH
Ullum H
BS
Burgess S
GD
Gill D
GK
Gallagher K
SM
Sabater-Lleal M
SI
Surakka I
JG
Jones GT
BM
Bown MJ
TP
Tsao PS
WC
Willer CJ
DS
Damrauer SM
Chapter II

Abstract

Summary of the research findings

Abdominal aortic aneurysm (AAA) is a common disease with substantial heritability. In this study, we performed a genome-wide association meta-analysis from 14 discovery cohorts and uncovered 141 independent associations, including 97 previously unreported loci. A polygenic risk score derived from meta-analysis explained AAA risk beyond clinical risk factors. Genes at AAA risk loci indicate involvement of lipid metabolism, vascular development and remodeling, extracellular matrix dysregulation and inflammation as key mechanisms in AAA pathogenesis. These genes also indicate overlap between the development of AAA and other monogenic aortopathies, particularly via transforming growth factor β signaling. Motivated by the strong evidence for the role of lipid metabolism in AAA, we used Mendelian randomization to establish the central role of nonhigh-density lipoprotein cholesterol in AAA and identified the opportunity for repurposing of proprotein convertase, subtilisin/kexin-type 9 (PCSK9) inhibitors. This was supported by a study demonstrating that PCSK9 loss of function prevented the development of AAA in a preclinical mouse model.

37,214 European ancestry cases, 997,776 European ancestry controls, 2,007 African ancestry cases, 88,331 African ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1125328
Total Participants
GWAS
Study Type
No
Replicated
European, African unspecified
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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