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GWAS Study

Novel Genetic Variants Associated with Chronic Kidney Disease Progression.

Han M, Moon S, Lee S et al.

36720675 PubMed ID
GWAS Study Type
4236 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HM
Han M
MS
Moon S
LS
Lee S
KK
Kim K
AW
An WJ
RH
Ryu H
KE
Kang E
AJ
Ahn JH
SH
Sung HY
PY
Park YS
LS
Lee SE
LS
Lee SH
JK
Jeong KH
AC
Ahn C
KT
Kelly TN
HJ
Hsu JY
FH
Feldman HI
PS
Park SK
OK
Oh KH
Chapter II

Abstract

Summary of the research findings

Significance statement: eGFR slope has been used as a surrogate outcome for progression of CKD. However, genetic markers associated with eGFR slope among patients with CKD were unknown. We aimed to identify genetic susceptibility loci associated with eGFR slope. A two-phase genome-wide association study identified single nucleotide polymorphisms (SNPs) in TPPP and FAT1-LINC02374 , and 22 of them were used to derive polygenic risk scores that mark the decline of eGFR by disrupting binding of nearby transcription factors. This work is the first to identify the impact of TPPP and FAT1-LINC02374 on CKD progression, providing predictive markers for the decline of eGFR in patients with CKD.

1,738 East Asian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

4236
Total Participants
GWAS
Study Type
Yes
Replicated
1,339 European ancestry individuals, 1,159 African American individuals
Replication Participants
East Asian, European, African American or Afro-Caribbean
Ancestry
Republic of Korea, U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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