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GWAS Study

Genetic analysis of elevated levels of creatinine and cystatin C biomarkers reveals novel genetic loci associated with kidney function.

D'Antonio M, Arthur TD, Gonzalez Rivera WG et al.

39927731 PubMed ID
GWAS Study Type
40170 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DM
D'Antonio M
AT
Arthur TD
GR
Gonzalez Rivera WG
WX
Wu X
NJ
Nguyen JP
GM
Gymrek M
WP
Woo-Yeong P
FK
Frazer KA
Chapter II

Abstract

Summary of the research findings

The rising prevalence of chronic kidney disease (CKD), affecting an estimated 37 million adults in the United States, presents a significant global health challenge. CKD is typically assessed using estimated Glomerular Filtration Rate (eGFR), which incorporates serum levels of biomarkers such as creatinine and cystatin C. However, these biomarkers do not directly measure kidney function; their elevation in CKD results from diminished glomerular filtration. Genome-wide association studies (GWAS) based on eGFR formulas using creatinine (eGFRcre) or cystatin C (eGFRcys) have identified distinct non-overlapping loci, raising questions about whether these loci govern kidney function or biomarker metabolism. In this study, we show that GWAS on creatinine and cystatin C levels in healthy individuals reveal both nonoverlapping genetic loci impacting their metabolism as well as overlapping genetic loci associated with kidney function; whereas GWAS on elevated levels of these biomarkers uncover novel loci primarily associated with kidney function in CKD patients.

40,170 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

40170
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

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