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Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas.

Title: Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas.
Authors: Hughes, O; Bentley, AR; Breeze, CE; Aguet, F; Xu, X; Nadkarni, G; Sun, Q; Lin, BM; Gilliland, T; Meyer, MC; Du, J; Raffield, LM; Kramer, H; Morton, RW; Gouveia, MH; Atkinson, EG; Valladares-Salgado, A; Wacher-Rodarte, N; Dueker, ND; Guo, X; Hai, Y; Adeyemo, A; Best, LG; Cai, J; Chen, G; Chong, M; Doumatey, A; Eales, J; Goodarzi, MO; Ipp, E; Irvin, MR; Jiang, M; Jones, AC; Kooperberg, C; Krieger, JE; Lange, EM; Lanktree, MB; Lash, JP; Lotufo, PA; Loos, RJF; Ha, My VT; Peralta-Romero, J; Qi, L; Raffel, LJ; Rich, SS; Rodriquez, EJ; Tarazona-Santos, E; Taylor, KD; Umans, JG; Wen, J; Young, BA
Source: Hughes, O, Bentley, AR, Breeze, CE, Aguet, F, Xu, X, Nadkarni, G, Sun, Q, Lin, BM, Gilliland, T, Meyer, MC, Du, J, Raffield, LM, Kramer, H, Morton, RW, Gouveia, MH, Atkinson, EG, Valladares-Salgado, A, Wacher-Rodarte, N, Dueker, ND, Guo, X, Hai, Y, Adeyemo, A, Best, LG, Cai, J, Chen, G, Chong, M, Doumatey, A, Eales, J, Goodarzi, MO, Ipp, E, Irvin, MR, Jiang, M, Jones, AC, Kooperberg, C, Krieger, JE, Lange, EM, Lanktree, MB, Lash, JP, Lotufo, PA, Loos, RJF, Ha, M VT, Peralta-Romero, J, Qi, L, Raffel, LJ, Rich, SS, Rodriquez, EJ, Tarazona-Santos, E, Taylor, KD, Umans, JG, ....
Publication Year: 2024
Collection: The University of Manchester: Research Explorer - Publications
Subject Terms: admixed populations; chronic kidney disease; eGFR; expression quantitative trait locus; fine-mapping; genome-wide association study; kidney function; multi-ancestry; polygenic scores
Description: Chronic kidney disease is a leading cause of death and disability globally and impacts individuals of African ancestry (AFR) or with ancestry in the Americas (AMS) who are under-represented in genome-wide association studies (GWASs) of kidney function. To address this bias, we conducted a large meta-analysis of GWASs of estimated glomerular filtration rate (eGFR) in 145,732 AFR and AMS individuals. We identified 41 loci at genome-wide significance (p < 5 × 10−8), of which two have not been previously reported in any ancestry group. We integrated fine-mapped loci with epigenomic and transcriptomic resources to highlight potential effector genes relevant to kidney physiology and disease, and reveal key regulatory elements and pathways involved in renal function and development. We demonstrate the varying but increased predictive power offered by a multi-ancestry polygenic score for eGFR and highlight the importance of population diversity in GWASs and multi-omics resources to enhance opportunities for clinical translation for all.
Document Type: article in journal/newspaper
Language: English
ISSN: 2666-979X
Relation: info:eu-repo/semantics/altIdentifier/pmid/38190104; info:eu-repo/semantics/altIdentifier/pissn/2666-979X
DOI: 10.1016/j.xgen.2023.100468
Availability: https://research.manchester.ac.uk/en/publications/09719049-c150-4a83-bd37-d5385eafa56c; https://doi.org/10.1016/j.xgen.2023.100468; https://europepmc.org/articles/PMC10794846
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by-nc-nd/4.0/
Accession Number: edsbas.F13CBF51
Database: BASE