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GWAS Study

Genome-wide association study of PR interval.

Pfeufer A, van Noord C, Marciante KD et al.

20062060 PubMed ID
GWAS Study Type
28517 Participants
162 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PA
Pfeufer A
VN
van Noord C
MK
Marciante KD
AD
Arking DE
LM
Larson MG
SA
Smith AV
TK
Tarasov KV
MM
Müller M
SN
Sotoodehnia N
SM
Sinner MF
VG
Verwoert GC
LM
Li M
KW
Kao WH
KA
Köttgen A
CJ
Coresh J
BJ
Bis JC
PB
Psaty BM
RK
Rice K
RJ
Rotter JI
RF
Rivadeneira F
HA
Hofman A
KJ
Kors JA
SB
Stricker BH
UA
Uitterlinden AG
VD
van Duijn CM
BB
Beckmann BM
SW
Sauter W
GC
Gieger C
LS
Lubitz SA
NC
Newton-Cheh C
WT
Wang TJ
MJ
Magnani JW
SR
Schnabel RB
CM
Chung MK
BJ
Barnard J
SJ
Smith JD
VW
Van Wagoner DR
VR
Vasan RS
AT
Aspelund T
EG
Eiriksdottir G
HT
Harris TB
LL
Launer LJ
NS
Najjar SS
LE
Lakatta E
SD
Schlessinger D
UM
Uda M
AG
Abecasis GR
MB
Müller-Myhsok B
EG
Ehret GB
BE
Boerwinkle E
CA
Chakravarti A
SE
Soliman EZ
LK
Lunetta KL
PS
Perz S
WH
Wichmann HE
MT
Meitinger T
LD
Levy D
GV
Gudnason V
EP
Ellinor PT
SS
Sanna S
KS
Kääb S
WJ
Witteman JC
AA
Alonso A
BE
Benjamin EJ
HS
Heckbert SR
Chapter II

Abstract

Summary of the research findings

The electrocardiographic PR interval (or PQ interval) reflects atrial and atrioventricular nodal conduction, disturbances of which increase risk of atrial fibrillation. We report a meta-analysis of genome-wide association studies for PR interval from seven population-based European studies in the CHARGE Consortium: AGES, ARIC, CHS, FHS, KORA, Rotterdam Study, and SardiNIA (N = 28,517). We identified nine loci associated with PR interval at P < 5 x 10(-8). At the 3p22.2 locus, we observed two independent associations in voltage-gated sodium channel genes, SCN10A and SCN5A. Six of the loci were near cardiac developmental genes, including CAV1-CAV2, NKX2-5 (CSX1), SOX5, WNT11, MEIS1, and TBX5-TBX3, providing pathophysiologically interesting candidate genes. Five of the loci, SCN5A, SCN10A, NKX2-5, CAV1-CAV2, and SOX5, were also associated with atrial fibrillation (N = 5,741 cases, P < 0.0056). This suggests a role for common variation in ion channel and developmental genes in atrial and atrioventricular conduction as well as in susceptibility to atrial fibrillation.

28,517 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

28517
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

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