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GWAS Study

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

Tin A, Marten J, Halperin Kuhns VL et al.

31578528 PubMed ID
GWAS Study Type
457690 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TA
Tin A
MJ
Marten J
HK
Halperin Kuhns VL
LY
Li Y
WM
Wuttke M
KH
Kirsten H
SK
Sieber KB
QC
Qiu C
GM
Gorski M
YZ
Yu Z
GA
Giri A
SG
Sveinbjornsson G
LM
Li M
CA
Chu AY
HA
Hoppmann A
OL
O'Connor LJ
PB
Prins B
NT
Nutile T
ND
Noce D
AM
Akiyama M
CM
Cocca M
GS
Ghasemi S
VD
van der Most PJ
HK
Horn K
XY
Xu Y
FC
Fuchsberger C
SS
Sedaghat S
AS
Afaq S
AN
Amin N
ÄJ
Ärnlöv J
BS
Bakker SJL
BN
Bansal N
BD
Baptista D
BS
Bergmann S
BM
Biggs ML
BG
Biino G
BE
Boerwinkle E
BE
Bottinger EP
BT
Boutin TS
BM
Brumat M
BR
Burkhardt R
CE
Campana E
CA
Campbell A
CH
Campbell H
CR
Carroll RJ
CE
Catamo E
CJ
Chambers JC
CM
Ciullo M
CM
Concas MP
CJ
Coresh J
CT
Corre T
CD
Cusi D
FS
Felicita SC
DB
de Borst MH
DG
De Grandi A
DM
de Mutsert R
DV
de Vries APJ
DG
Delgado G
DA
Demirkan A
DO
Devuyst O
DK
Dittrich K
EK
Eckardt KU
EG
Ehret G
EK
Endlich K
EM
Evans MK
GR
Gansevoort RT
GP
Gasparini P
GV
Giedraitis V
GC
Gieger C
GG
Girotto G
GM
Gögele M
GS
Gordon SD
GD
Gudbjartsson DF
GV
Gudnason V
HT
Haller T
HP
Hamet P
HT
Harris TB
HC
Hayward C
HA
Hicks AA
HE
Hofer E
HH
Holm H
HW
Huang W
HN
Hutri-Kähönen N
HS
Hwang SJ
IM
Ikram MA
LR
Lewis RM
IE
Ingelsson E
JJ
Jakobsdottir J
JI
Jonsdottir I
JH
Jonsson H
JP
Joshi PK
JN
Josyula NS
JB
Jung B
KM
Kähönen M
KY
Kamatani Y
KM
Kanai M
KS
Kerr SM
KW
Kiess W
KM
Kleber ME
KW
Koenig W
KJ
Kooner JS
KA
Körner A
KP
Kovacs P
KB
Krämer BK
KF
Kronenberg F
KM
Kubo M
KB
Kühnel B
LB
La Bianca M
LL
Lange LA
LB
Lehne B
LT
Lehtimäki T
LJ
Liu J
LM
Loeffler M
LR
Loos RJF
LL
Lyytikäinen LP
MR
Magi R
MA
Mahajan A
MN
Martin NG
MW
März W
MD
Mascalzoni D
MK
Matsuda K
MC
Meisinger C
MT
Meitinger T
MA
Metspalu A
MY
Milaneschi Y
OC
O'Donnell CJ
WO
Wilson OD
GJ
Gaziano JM
MP
Mishra PP
MK
Mohlke KL
MN
Mononen N
MG
Montgomery GW
MD
Mook-Kanamori DO
MM
Müller-Nurasyid M
NG
Nadkarni GN
NM
Nalls MA
NM
Nauck M
NK
Nikus K
NB
Ning B
NI
Nolte IM
NR
Noordam R
OJ
O'Connell JR
OI
Olafsson I
PS
Padmanabhan S
PB
Penninx BWJH
PT
Perls T
PA
Peters A
PM
Pirastu M
PN
Pirastu N
PG
Pistis G
PO
Polasek O
PB
Ponte B
PD
Porteous DJ
PT
Poulain T
PM
Preuss MH
RT
Rabelink TJ
RL
Raffield LM
RO
Raitakari OT
RR
Rettig R
RM
Rheinberger M
RK
Rice KM
RF
Rizzi F
RA
Robino A
RI
Rudan I
KA
Krajcoviechova A
CR
Cifkova R
RR
Rueedi R
RD
Ruggiero D
RK
Ryan KA
SY
Saba Y
SE
Salvi E
SH
Schmidt H
SR
Schmidt R
SC
Shaffer CM
SA
Smith AV
SB
Smith BH
SC
Spracklen CN
SK
Strauch K
SM
Stumvoll M
SP
Sulem P
TS
Tajuddin SM
TA
Teren A
TJ
Thiery J
TC
Thio CHL
TU
Thorsteinsdottir U
TD
Toniolo D
TA
Tönjes A
TJ
Tremblay J
UA
Uitterlinden AG
VS
Vaccargiu S
VD
van der Harst P
VD
van Duijn CM
VN
Verweij N
VU
Völker U
VP
Vollenweider P
WG
Waeber G
WM
Waldenberger M
WJ
Whitfield JB
WS
Wild SH
WJ
Wilson JF
YQ
Yang Q
ZW
Zhang W
ZA
Zonderman AB
BM
Bochud M
WJ
Wilson JG
PS
Pendergrass SA
HK
Ho K
PA
Parsa A
PP
Pramstaller PP
PB
Psaty BM
BC
Böger CA
SH
Snieder H
BA
Butterworth AS
OY
Okada Y
ET
Edwards TL
SK
Stefansson K
SK
Susztak K
SM
Scholz M
HI
Heid IM
HA
Hung AM
TA
Teumer A
PC
Pattaro C
WO
Woodward OM
VV
Vitart V
KA
Köttgen A
Chapter II

Abstract

Summary of the research findings

Elevated serum urate levels cause gout and correlate with cardiometabolic diseases via poorly understood mechanisms. We performed a trans-ancestry genome-wide association study of serum urate in 457,690 individuals, identifying 183 loci (147 previously unknown) that improve the prediction of gout in an independent cohort of 334,880 individuals. Serum urate showed significant genetic correlations with many cardiometabolic traits, with genetic causality analyses supporting a substantial role for pleiotropy. Enrichment analysis, fine-mapping of urate-associated loci and colocalization with gene expression in 47 tissues implicated the kidney and liver as the main target organs and prioritized potentially causal genes and variants, including the transcriptional master regulators in the liver and kidney, HNF1A and HNF4A. Experimental validation showed that HNF4A transactivated the promoter of ABCG2, encoding a major urate transporter, in kidney cells, and that HNF4A p.Thr139Ile is a functional variant. Transcriptional coregulation within and across organs may be a general mechanism underlying the observed pleiotropy between urate and cardiometabolic traits.

288,649 European ancestry individuals, 125,725 East Asian ancestry individuals, 33,671 African American individuals, 9,037 South Asian ancestry individuals, 608 Hispanic individuals

Chapter III

Study Statistics

Key metrics and study information

457690
Total Participants
GWAS
Study Type
No
Replicated
South Asian, African American or Afro-Caribbean, European, East Asian, Hispanic or Latin American, NR
Ancestry
U.S.
Recruitment Country
Chapter IV

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