Menu
GWAS Study

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.

Gorski M, Jung B, Li Y et al.

33137338 PubMed ID
GWAS Study Type
141964 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GM
Gorski M
JB
Jung B
LY
Li Y
MP
Matias-Garcia PR
WM
Wuttke M
CS
Coassin S
TC
Thio CHL
KM
Kleber ME
WT
Winkler TW
WV
Wanner V
CJ
Chai JF
CA
Chu AY
CM
Cocca M
FM
Feitosa MF
GS
Ghasemi S
HA
Hoppmann A
HK
Horn K
LM
Li M
NT
Nutile T
SM
Scholz M
SK
Sieber KB
TA
Teumer A
TA
Tin A
WJ
Wang J
TB
Tayo BO
AT
Ahluwalia TS
AP
Almgren P
BS
Bakker SJL
BB
Banas B
BN
Bansal N
BM
Biggs ML
BE
Boerwinkle E
BE
Bottinger EP
BH
Brenner H
CR
Carroll RJ
CJ
Chalmers J
CM
Chee ML
CM
Chee ML
CC
Cheng CY
CJ
Coresh J
DB
de Borst MH
DF
Degenhardt F
EK
Eckardt KU
EK
Endlich K
FA
Franke A
FS
Freitag-Wolf S
GP
Gampawar P
GR
Gansevoort RT
GM
Ghanbari M
GC
Gieger C
HP
Hamet P
HK
Ho K
HE
Hofer E
HB
Holleczek B
XF
Xian Foo VH
HN
Hutri-Kähönen N
HS
Hwang SJ
IM
Ikram MA
JN
Josyula NS
KM
Kähönen M
KC
Khor CC
KW
Koenig W
KH
Kramer H
KB
Krämer BK
KB
Kühnel B
LL
Lange LA
LT
Lehtimäki T
LW
Lieb W
LR
Loos RJF
LM
Lukas MA
LL
Lyytikäinen LP
MC
Meisinger C
MT
Meitinger T
MO
Melander O
MY
Milaneschi Y
MP
Mishra PP
MN
Mononen N
MJ
Mychaleckyj JC
NG
Nadkarni GN
NM
Nauck M
NK
Nikus K
NB
Ning B
NI
Nolte IM
OM
O'Donoghue ML
OM
Orho-Melander M
PS
Pendergrass SA
PB
Penninx BWJH
PM
Preuss MH
PB
Psaty BM
RL
Raffield LM
RO
Raitakari OT
RR
Rettig R
RM
Rheinberger M
RK
Rice KM
RA
Rosenkranz AR
RP
Rossing P
RJ
Rotter JI
SC
Sabanayagam C
SH
Schmidt H
SR
Schmidt R
SB
Schöttker B
SC
Schulz CA
SS
Sedaghat S
SC
Shaffer CM
SK
Strauch K
SS
Szymczak S
TK
Taylor KD
TJ
Tremblay J
CL
Chaker L
VD
van der Harst P
VD
van der Most PJ
VN
Verweij N
VU
Völker U
WM
Waldenberger M
WL
Wallentin L
WD
Waterworth DM
WH
White HD
WJ
Wilson JG
WT
Wong TY
WM
Woodward M
YQ
Yang Q
YM
Yasuda M
YL
Yerges-Armstrong LM
ZY
Zhang Y
SH
Snieder H
WC
Wanner C
BC
Böger CA
KA
Köttgen A
KF
Kronenberg F
PC
Pattaro C
HI
Heid IM
Chapter II

Abstract

Summary of the research findings

Rapid decline of glomerular filtration rate estimated from creatinine (eGFRcrea) is associated with severe clinical endpoints. In contrast to cross-sectionally assessed eGFRcrea, the genetic basis for rapid eGFRcrea decline is largely unknown. To help define this, we meta-analyzed 42 genome-wide association studies from the Chronic Kidney Diseases Genetics Consortium and United Kingdom Biobank to identify genetic loci for rapid eGFRcrea decline. Two definitions of eGFRcrea decline were used: 3 mL/min/1.73m2/year or more ("Rapid3"; encompassing 34,874 cases, 107,090 controls) and eGFRcrea decline 25% or more and eGFRcrea under 60 mL/min/1.73m2 at follow-up among those with eGFRcrea 60 mL/min/1.73m2 or more at baseline ("CKDi25"; encompassing 19,901 cases, 175,244 controls). Seven independent variants were identified across six loci for Rapid3 and/or CKDi25: consisting of five variants at four loci with genome-wide significance (near UMOD-PDILT (2), PRKAG2, WDR72, OR2S2) and two variants among 265 known eGFRcrea variants (near GATM, LARP4B). All these loci were novel for Rapid3 and/or CKDi25 and our bioinformatic follow-up prioritized variants and genes underneath these loci. The OR2S2 locus is novel for any eGFRcrea trait including interesting candidates. For the five genome-wide significant lead variants, we found supporting effects for annual change in blood urea nitrogen or cystatin-based eGFR, but not for GATM or LARP4B. Individuals at high compared to those at low genetic risk (8-14 vs. 0-5 adverse alleles) had a 1.20-fold increased risk of acute kidney injury (95% confidence interval 1.08-1.33). Thus, our identified loci for rapid kidney function decline may help prioritize therapeutic targets and identify mechanisms and individuals at risk for sustained deterioration of kidney function.

34,874 European, African American, Hispanic or South Asian cases, 107,090 European, African American, Hispanic or South Asian controls

Chapter III

Study Statistics

Key metrics and study information

141964
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean, European, Hispanic or Latin American, South Asian
Ancestry
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.