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GWAS Study

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.

Liu C, Kraja AT, Smith JA et al.

27618448 PubMed ID
GWAS Study Type
327288 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LC
Liu C
KA
Kraja AT
SJ
Smith JA
BJ
Brody JA
FN
Franceschini N
BJ
Bis JC
RK
Rice K
MA
Morrison AC
LY
Lu Y
WS
Weiss S
GX
Guo X
PW
Palmas W
ML
Martin LW
CY
Chen YD
SP
Surendran P
DF
Drenos F
CJ
Cook JP
AP
Auer PL
CA
Chu AY
GA
Giri A
ZW
Zhao W
JJ
Jakobsdottir J
LL
Lin LA
SJ
Stafford JM
AN
Amin N
MH
Mei H
YJ
Yao J
VA
Voorman A
LM
Larson MG
GM
Grove ML
SA
Smith AV
HS
Hwang SJ
CH
Chen H
HT
Huan T
KG
Kosova G
SN
Stitziel NO
KS
Kathiresan S
SN
Samani N
SH
Schunkert H
DP
Deloukas P
LM
Li M
FC
Fuchsberger C
PC
Pattaro C
GM
Gorski M
KC
Kooperberg C
PG
Papanicolaou GJ
RJ
Rossouw JE
FJ
Faul JD
KS
Kardia SL
BC
Bouchard C
RL
Raffel LJ
UA
Uitterlinden AG
FO
Franco OH
VR
Vasan RS
OC
O'Donnell CJ
TK
Taylor KD
LK
Liu K
BE
Bottinger EP
GO
Gottesman O
DE
Daw EW
GF
Giulianini F
GS
Ganesh S
SE
Salfati E
HT
Harris TB
LL
Launer LJ
DM
Dörr M
FS
Felix SB
RR
Rettig R
VH
Völzke H
KE
Kim E
LW
Lee WJ
LI
Lee IT
SW
Sheu WH
TK
Tsosie KS
ED
Edwards DR
LY
Liu Y
CA
Correa A
WD
Weir DR
VU
Völker U
RP
Ridker PM
BE
Boerwinkle E
GV
Gudnason V
RA
Reiner AP
VD
van Duijn CM
BI
Borecki IB
ET
Edwards TL
CA
Chakravarti A
RJ
Rotter JI
PB
Psaty BM
LR
Loos RJ
FM
Fornage M
EG
Ehret GB
NC
Newton-Cheh C
LD
Levy D
CD
Chasman DI
Chapter II

Abstract

Summary of the research findings

Meta-analyses of association results for blood pressure using exome-centric single-variant and gene-based tests identified 31 new loci in a discovery stage among 146,562 individuals, with follow-up and meta-analysis in 180,726 additional individuals (total n = 327,288). These blood pressure-associated loci are enriched for known variants for cardiometabolic traits. Associations were also observed for the aggregation of rare and low-frequency missense variants in three genes, NPR1, DBH, and PTPMT1. In addition, blood pressure associations at 39 previously reported loci were confirmed. The identified variants implicate biological pathways related to cardiometabolic traits, vascular function, and development. Several new variants are inferred to have roles in transcription or as hubs in protein-protein interaction networks. Genetic risk scores constructed from the identified variants were strongly associated with coronary disease and myocardial infarction. This large collection of blood pressure-associated loci suggests new therapeutic strategies for hypertension, emphasizing a link with cardiometabolic risk.

120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals

Chapter III

Study Statistics

Key metrics and study information

327288
Total Participants
GWAS
Study Type
Yes
Replicated
154,543 European ancestry individuals, 26,183 South Asian ancestry individuals
Replication Participants
South Asian, African American or Afro-Caribbean, Hispanic or Latin American, European
Ancestry
Bangladesh, Pakistan, U.S., France, Germany, Netherlands, Denmark, Finland, Republic of Ireland, Norway, Sweden, U.K., Greece, Italy, Spain, Iceland
Recruitment Country
Chapter IV

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