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Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos.

Citation
Qian, H., et al. “Genome-Wide Association Of Kidney Traits In Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study Of Latinos.”. Circulation. Genomic And Precision Medicine, p. e002891.
Center UCSD-UCLA
Author Huijun Qian, Madeline H Kowalski, Holly J Kramer, Ran Tao, James P Lash, Adrienne M Stilp, Jianwen Cai, Yun Li, Nora Franceschini
Keywords genes, genetic variation, Genetics, genome-wide association study, Kidney, population
Abstract

BACKGROUND: Genetic factors that influence kidney traits have been understudied for low-frequency and ancestry-specific variants.

METHODS: This study used imputed whole-genome sequencing from the Trans-Omics for Precision Medicine project to identify novel loci for estimated glomerular filtration rate and urine albumin-to-creatinine ratio in up to 12 207 Hispanics/Latinos. Replication was performed in the Women's Health Initiative and the UK Biobank when variants were available.

RESULTS: Two low-frequency intronic variants were associated with estimated glomerular filtration rate (rs58720902 at , minor allele frequency=0.01, =1.6×10) or urine albumin-to-creatinine ratio (rs527493184 at , minor allele frequency=0.002, =1.1×10). An additional variant at (rs2422935, minor allele frequency=0.54, =2.89×10) was significantly associated with estimated glomerular filtration rate in meta-analysis with replication samples. We also identified 2 known loci for urine albumin-to-creatinine ratio ( rs116907128, =5.6×10 and rs344, =9.3×10) and validated 8 loci for urine albumin-to-creatinine ratio previously identified in the UK Biobank.

CONCLUSIONS: Our study shows gains in gene discovery when using dense imputation from multi-ethnic whole-genome sequencing data in admixed Hispanics/Latinos. It also highlights limitations in genetic research of kidney traits, including the lack of suitable replication samples for variants that are more common in non-European ancestry and those at low frequency in populations.

Year of Publication
2020
Journal
Circulation. Genomic and precision medicine
Volume
13
Issue
4
Number of Pages
e002891
Date Published
08/2020
ISSN Number
2574-8300
DOI
10.1161/CIRCGEN.119.002891
Alternate Journal
Circ Genom Precis Med
PMID
32600054
PMCID
PMC7442703
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