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GWAS Study

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

Keaton JM, Kamali Z, Xie T et al.

38689001 PubMed ID
GWAS Study Type
1091027 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KJ
Keaton JM
KZ
Kamali Z
XT
Xie T
VA
Vaez A
WA
Williams A
GS
Goleva SB
AA
Ani A
EE
Evangelou E
HJ
Hellwege JN
YL
Yengo L
YW
Young WJ
TM
Traylor M
GA
Giri A
ZZ
Zheng Z
ZJ
Zeng J
CD
Chasman DI
MA
Morris AP
CM
Caulfield MJ
HS
Hwang SJ
KJ
Kooner JS
CD
Conen D
AJ
Attia JR
MA
Morrison AC
LR
Loos RJF
KK
Kristiansson K
SR
Schmidt R
HA
Hicks AA
PP
Pramstaller PP
NC
Nelson CP
SN
Samani NJ
RL
Risch L
GU
Gyllensten U
MO
Melander O
RH
Riese H
WJ
Wilson JF
CH
Campbell H
RS
Rich SS
PB
Psaty BM
LY
Lu Y
RJ
Rotter JI
GX
Guo X
RK
Rice KM
VP
Vollenweider P
SJ
Sundström J
LC
Langenberg C
TM
Tobin MD
GV
Giedraitis V
LJ
Luan J
TJ
Tuomilehto J
KZ
Kutalik Z
RS
Ripatti S
SV
Salomaa V
GG
Girotto G
TS
Trompet S
JJ
Jukema JW
VD
van der Harst P
RP
Ridker PM
GF
Giulianini F
VV
Vitart V
GA
Goel A
WH
Watkins H
HS
Harris SE
DI
Deary IJ
VD
van der Most PJ
OA
Oldehinkel AJ
KB
Keavney BD
HC
Hayward C
CA
Campbell A
BM
Boehnke M
SL
Scott LJ
BT
Boutin T
MC
Mamasoula C
JM
Järvelin MR
PA
Peters A
GC
Gieger C
LE
Lakatta EG
CF
Cucca F
HJ
Hui J
KP
Knekt P
ES
Enroth S
DB
De Borst MH
PO
Polašek O
CM
Concas MP
CE
Catamo E
CM
Cocca M
LR
Li-Gao R
HE
Hofer E
SH
Schmidt H
SB
Spedicati B
WM
Waldenberger M
SD
Strachan DP
LM
Laan M
TA
Teumer A
DM
Dörr M
GV
Gudnason V
CJ
Cook JP
RD
Ruggiero D
KI
Kolcic I
BE
Boerwinkle E
TM
Traglia M
LT
Lehtimäki T
RO
Raitakari OT
JA
Johnson AD
NC
Newton-Cheh C
BM
Brown MJ
DA
Dominiczak AF
SP
Sever PJ
PN
Poulter N
CJ
Chambers JC
ER
Elosua R
SD
Siscovick D
ET
Esko T
MA
Metspalu A
SR
Strawbridge RJ
LM
Laakso M
HA
Hamsten A
HJ
Hottenga JJ
DG
de Geus E
MA
Morris AD
PC
Palmer CNA
NI
Nolte IM
MY
Milaneschi Y
MJ
Marten J
WA
Wright A
ZE
Zeggini E
HJ
Howson JMM
OC
O'Donnell CJ
ST
Spector T
NM
Nalls MA
SE
Simonsick EM
LY
Liu Y
VD
van Duijn CM
BA
Butterworth AS
DJ
Danesh JN
MC
Menni C
WN
Wareham NJ
KK
Khaw KT
SY
Sun YV
WP
Wilson PWF
CK
Cho K
VP
Visscher PM
DJ
Denny JC
LD
Levy D
ET
Edwards TL
MP
Munroe PB
SH
Snieder H
WH
Warren HR
Chapter II

Abstract

Summary of the research findings

Hypertension affects more than one billion people worldwide. Here we identify 113 novel loci, reporting a total of 2,103 independent genetic signals (P < 5 × 10-8) from the largest single-stage blood pressure (BP) genome-wide association study to date (n = 1,028,980 European individuals). These associations explain more than 60% of single nucleotide polymorphism-based BP heritability. Comparing top versus bottom deciles of polygenic risk scores (PRSs) reveals clinically meaningful differences in BP (16.9 mmHg systolic BP, 95% CI, 15.5-18.2 mmHg, P = 2.22 × 10-126) and more than a sevenfold higher odds of hypertension risk (odds ratio, 7.33; 95% CI, 5.54-9.70; P = 4.13 × 10-44) in an independent dataset. Adding PRS into hypertension-prediction models increased the area under the receiver operating characteristic curve (AUROC) from 0.791 (95% CI, 0.781-0.801) to 0.826 (95% CI, 0.817-0.836, ∆AUROC, 0.035, P = 1.98 × 10-34). We compare the 2,103 loci results in non-European ancestries and show significant PRS associations in a large African-American sample. Secondary analyses implicate 500 genes previously unreported for BP. Our study highlights the role of increasingly large genomic studies for precision health research.

1,028,980 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

1091027
Total Participants
GWAS
Study Type
Yes
Replicated
40,204 African ancestry individuals, 21,843 African American individuals
Replication Participants
European, African unspecified, African American or Afro-Caribbean
Ancestry
U.S., U.K.
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.