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Genome-wide association study meta-analysis of blood pressure traits and hypertension in sub-Saharan African populations: an AWI-Gen study.

Authors :
Singh, Surina
Choudhury, Ananyo
Hazelhurst, Scott
Crowther, Nigel J.
Boua, Palwendé R.
Sorgho, Hermann
Agongo, Godfred
Nonterah, Engelbert A.
Micklesfield, Lisa K.
Norris, Shane A.
Kisiangani, Isaac
Mohamed, Shukri
Gómez-Olivé, Francesc X.
Tollman, Stephen M.
Choma, Solomon
Brandenburg, J-T.
Ramsay, Michèle
Source :
Nature Communications; 12/16/2023, Vol. 14 Issue 1, p1-14, 14p
Publication Year :
2023

Abstract

Most hypertension-related genome-wide association studies (GWASs) focus on non-African populations, despite hypertension (a major risk factor for cardiovascular disease) being highly prevalent in Africa. The AWI-Gen study GWAS meta-analysis for blood pressure (BP)-related traits (systolic and diastolic BP, pulse pressure, mean-arterial pressure and hypertension) from three sub-Saharan African geographic regions (N = 10,775), identifies two novel genome-wide significant signals (p < 5E-08): systolic BP near P2RY1 (rs77846204; intergenic variant, p = 4.95E-08) and pulse pressure near LINC01256 (rs80141533; intergenic variant, p = 1.76E-08). No genome-wide signals are detected for the AWI-Gen GWAS meta-analysis with previous African-ancestry GWASs (UK Biobank (African), Uganda Genome Resource). Suggestive signals (p < 5E-06) are observed for all traits, with 29 SNPs associating with more than one trait and several replicating known associations. Polygenic risk scores (PRSs) developed from studies on different ancestries have limited transferability, with multi-ancestry PRS providing better prediction. This study provides insights into the genetics of BP variation in African populations. Hypertension is a major risk factor for cardiovascular disease prevalent in Africa. Here the authors report a genome-wide study providing insights into the genetics and physiology of blood pressure variation in African populations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
174267980
Full Text :
https://doi.org/10.1038/s41467-023-44079-0