| Literature DB >> 32409295 |
Adrienne Tin1,2, Anna Köttgen3,4.
Abstract
The past few years have seen major advances in genome-wide association studies (GWAS) of CKD and kidney function-related traits in several areas: increases in sample size from >100,000 to >1 million, enabling the discovery of >250 associated genetic loci that are highly reproducible; the inclusion of participants not only of European but also of non-European ancestries; and the use of advanced computational methods to integrate additional genomic and other unbiased, high-dimensional data to characterize the underlying genetic architecture and prioritize potentially causal genes and variants. Together with other large-scale biobank and genetic association studies of complex traits, these GWAS of kidney function-related traits have also provided novel insight into the relationship of kidney function to other diseases with respect to their genetic associations, genetic correlation, and directional relationships. A number of studies also included functional experiments using model organisms or cell lines to validate prioritized potentially causal genes and/or variants. In this review article, we will summarize these recent GWAS of CKD and kidney function-related traits, explain approaches for downstream characterization of associated genetic loci and the value of such computational follow-up analyses, and discuss related challenges along with potential solutions to ultimately enable improved treatment and prevention of kidney diseases through genetics.Entities:
Keywords: Biological Specimen Banks; Cell Line; Chronic; Follow-Up Studies; Genetic Association Studies; Genetic Loci; Genome; Genome-Wide Association Study; Genomics; Kidney Genomics Series; Multifactorial Inheritance; Renal Insufficiency; Sample Size; chronic kidney disease; genetic renal disease
Year: 2020 PMID: 32409295 PMCID: PMC7646230 DOI: 10.2215/CJN.00020120
Source DB: PubMed Journal: Clin J Am Soc Nephrol ISSN: 1555-9041 Impact factor: 8.237