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GWAS Study

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.

Gretarsdottir S, Baas AF, Thorleifsson G et al.

20622881 PubMed ID
GWAS Study Type
42513 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GS
Gretarsdottir S
BA
Baas AF
TG
Thorleifsson G
HH
Holm H
DH
den Heijer M
DV
de Vries JP
KS
Kranendonk SE
ZC
Zeebregts CJ
VS
van Sterkenburg SM
GR
Geelkerken RH
VR
van Rij AM
WM
Williams MJ
BA
Boll AP
KJ
Kostic JP
JA
Jonasdottir A
JA
Jonasdottir A
WG
Walters GB
MG
Masson G
SP
Sulem P
SJ
Saemundsdottir J
MM
Mouy M
MK
Magnusson KP
TG
Tromp G
EJ
Elmore JR
SN
Sakalihasan N
LR
Limet R
DJ
Defraigne JO
FR
Ferrell RE
RA
Ronkainen A
RY
Ruigrok YM
WC
Wijmenga C
GD
Grobbee DE
SS
Shah SH
GC
Granger CB
QA
Quyyumi AA
VV
Vaccarino V
PR
Patel RS
ZA
Zafari AM
LA
Levey AI
AH
Austin H
GD
Girelli D
PP
Pignatti PF
OO
Olivieri O
MN
Martinelli N
MG
Malerba G
TE
Trabetti E
BL
Becker LC
BD
Becker DM
RM
Reilly MP
RD
Rader DJ
MT
Mueller T
DB
Dieplinger B
HM
Haltmayer M
US
Urbonavicius S
LB
Lindblad B
GA
Gottsäter A
GE
Gaetani E
PR
Pola R
WP
Wells P
RM
Rodger M
FM
Forgie M
LN
Langlois N
CJ
Corral J
VV
Vicente V
FJ
Fontcuberta J
EF
España F
GN
Grarup N
JT
Jørgensen T
WD
Witte DR
HT
Hansen T
PO
Pedersen O
AK
Aben KK
DG
de Graaf J
HS
Holewijn S
FL
Folkersen L
FA
Franco-Cereceda A
EP
Eriksson P
CD
Collier DA
SH
Stefansson H
SV
Steinthorsdottir V
RT
Rafnar T
VE
Valdimarsson EM
MH
Magnadottir HB
SS
Sveinbjornsdottir S
OI
Olafsson I
MM
Magnusson MK
PR
Palmason R
HV
Haraldsdottir V
AK
Andersen K
OP
Onundarson PT
TG
Thorgeirsson G
KL
Kiemeney LA
PJ
Powell JT
CD
Carey DJ
KH
Kuivaniemi H
LJ
Lindholt JS
JG
Jones GT
KA
Kong A
BJ
Blankensteijn JD
MS
Matthiasson SE
TU
Thorsteinsdottir U
SK
Stefansson K
Chapter II

Abstract

Summary of the research findings

We performed a genome-wide association study on 1,292 individuals with abdominal aortic aneurysms (AAAs) and 30,503 controls from Iceland and The Netherlands, with a follow-up of top markers in up to 3,267 individuals with AAAs and 7,451 controls. The A allele of rs7025486 on 9q33 was found to associate with AAA, with an odds ratio (OR) of 1.21 and P = 4.6 x 10(-10). In tests for association with other vascular diseases, we found that rs7025486[A] is associated with early onset myocardial infarction (OR = 1.18, P = 3.1 x 10(-5)), peripheral arterial disease (OR = 1.14, P = 3.9 x 10(-5)) and pulmonary embolism (OR = 1.20, P = 0.00030), but not with intracranial aneurysm or ischemic stroke. No association was observed between rs7025486[A] and common risk factors for arterial and venous diseases-that is, smoking, lipid levels, obesity, type 2 diabetes and hypertension. Rs7025486 is located within DAB2IP, which encodes an inhibitor of cell growth and survival.

1,292 European ancestry cases, 30,503 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

42513
Total Participants
GWAS
Study Type
Yes
Replicated
3,267 European ancestry cases, 7,451 European ancestry controls
Replication Participants
European
Ancestry
U.S., Netherlands, Canada, Belgium, U.K., New Zealand, Denmark, Iceland
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.