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GWAS Study

Genome-Wide Association Study of Chronic Kidney Disease Progression.

Robinson-Cohen C, Triozzi JL, Rowan B et al.

37261792 PubMed ID
GWAS Study Type
116960 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RC
Robinson-Cohen C
TJ
Triozzi JL
RB
Rowan B
HJ
He J
CH
Chen HC
ZN
Zheng NS
WW
Wei WQ
WO
Wilson OD
HJ
Hellwege JN
TP
Tsao PS
GJ
Gaziano JM
BA
Bick A
MM
Matheny ME
CC
Chung CP
LL
Lipworth L
SE
Siew ED
IT
Ikizler TA
TR
Tao R
HA
Hung AM
Chapter II

Abstract

Summary of the research findings

Significance statement: Rapid progression of CKD is associated with poor clinical outcomes. Most previous studies looking for genetic factors associated with low eGFR have used cross-sectional data. The authors conducted a meta-analysis of genome-wide association studies of eGFR decline among 116,870 participants with CKD, focusing on longitudinal data. They identified three loci (two of them novel) associated with longitudinal eGFR decline. In addition to the known UMOD/PDILT locus, variants within BICC1 were associated with significant differences in longitudinal eGFR slope. Variants within HEATR4 also were associated with differences in eGFR decline, but only among Black/African American individuals without diabetes. These findings help characterize molecular mechanisms of eGFR decline in CKD and may inform new therapeutic approaches for progressive kidney disease.

18,319 African American or Afro-Caribbean individuals, 98,641 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

116960
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean, European
Ancestry
U.S.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

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