Genetic risk scores for cardiometabolic traits in sub-Saharan African populations. (17th March 2021)

• Record Type: Journal Article
• Authors: Ekoru, Kenneth; Adeyemo, Adebowale A; Chen, Guanjie; Doumatey, Ayo P; Zhou, Jie; Bentley, Amy R; Shriner, Daniel; Rotimi, Charles N
• Is Part Of: International journal of epidemiology. Volume 50:Number 4(2021)
• Page Start: 1283
• Page End: 1296
• Publication Date: 2021-03-17
• Subjects: Genetic risk score -- polygenic risk score -- sub-Sahara Africa -- cardiometabolic traits; Epidemiology -- Periodicals; 614.4
• DOI: 10.1093/ije/dyab046
• Languages: English
• ISSNs: 0300-5771

Abstract

Abstract: Background: There is growing support for the use of genetic risk scores (GRS) in routine clinical settings. Due to the limited diversity of current genomic discovery samples, there are concerns that the predictive power of GRS will be limited in non-European ancestry populations. GRS for cardiometabolic traits were evaluated in sub-Saharan Africans in comparison with African Americans and European Americans. Methods: We evaluated the predictive utility of GRS for 12 cardiometabolic traits in sub-Saharan Africans (AF; n = 5200), African Americans (AA; n = 9139) and European Americans (EUR; n = 9594). GRS were constructed as weighted sums of the number of risk alleles. Predictive utility was assessed using the additional phenotypic variance explained and the increase in discriminatory ability over traditional risk factors [age, sex and body mass index (BMI)], with adjustment for ancestry-derived principal components. Results: Across all traits, GRS showed up to a 5-fold and 20-fold greater predictive utility in EUR relative to AA and AF, respectively. Predictive utility was most consistent for lipid traits, with percentage increase in explained variation attributable to GRS ranging from 10.6% to 127.1% among EUR, 26.6% to 65.8% among AA and 2.4% to 37.5% among AF. These differences were recapitulated in the discriminatory power, whereby the predictive utility of GRS was 4-fold greater in EUR relative to AA and up to 44-fold greater in EUR relative to AF. Obesity and blood pressure traits showed a similar pattern of greater predictive utility among EUR. Conclusions: This work demonstrates the poorer performance of GRS in AF and highlights the need to improve representation of multiple ethnic populations in genomic studies to ensure equitable clinical translation of GRS.