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Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries

BACKGROUND: Polygenic scores (PGS) for coronary artery disease (CAD) measure a person's genetic liability for CAD. PGSs for CAD are generally considered sufficiently predictive in individuals of European ancestry, but their performance is attenuated in non-European ancestry groups (AGs). We col...

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Autores principales: Regazzi, L, Bolli, A, Cadeddu, C, Boccia, S, Busby, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596342/
http://dx.doi.org/10.1093/eurpub/ckad160.222
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author Regazzi, L
Bolli, A
Cadeddu, C
Boccia, S
Busby, G
author_facet Regazzi, L
Bolli, A
Cadeddu, C
Boccia, S
Busby, G
author_sort Regazzi, L
collection PubMed
description BACKGROUND: Polygenic scores (PGS) for coronary artery disease (CAD) measure a person's genetic liability for CAD. PGSs for CAD are generally considered sufficiently predictive in individuals of European ancestry, but their performance is attenuated in non-European ancestry groups (AGs). We collated publicly available CAD PGS and benchmarked their performance across several AGs to evaluate their utility for personalized prevention. METHODS: We queried the “PGS Catalog” to extract standardized odds/hazard ratios (OR/HR) for published CAD PGSs across multiple AGs (European-EUR, African-AFR, Hispanic-HIS, South-Asian-SAS, East-Asian-EAS). We restricted our analysis to PGSs specifically developed for prevalent and/or incident CAD and identified the five best-performing PGSs in each AG. We then computed these PGSs in a sample of 504,096 individuals of EUR (94.5%), AFR (2.6%), SAS (1.9%), EAS (0.7%) and HIS (0.3%) AG and evaluated their performance through logistic regression (covariates: age, sex, family history of CAD, principal components of AG). RESULTS: PGS000018 performed best in SAS (1.69[1.56-1.83]), EUR (1.62[1.60-1.64]) and EAS (1.45[1.11-1.89]). PGS001780 was the best performing PGS in AFR (1.18[1.04-1.33], on par with PGS000749) and ranked second in EUR (1.59[1.57-1.61]) and SAS (1.64[1.53-1.76]). Finally, PGS002262 was best in HIS (1.39[1.07-1.81], almost on par with PGS000337) and second in EASs (1.41[1.13-1.75]). Overall, the highest standardized ORs were found for the SAS and the EUR AGs, while the AFR AG had the worst performances. PGSs performed differently than previously reported both in an absolute and relative way, corroborating the need of a standardized comparison. CONCLUSIONS: There is currently no gold-standard trans-ancestry CAD PGS, but the employment of different AG-specific CAD PGSs can achieve the best possible predictive performance in every individual, an essential prerequisite towards implementing PGSs in CAD personalized prevention protocols. KEY MESSAGES: • No gold standard PGS for CAD exists that can be applied with equal predictive performance across all AGs, which can be partially counterbalance by using the best performing PGS in each AG. • In our analysis, the absolute performance of all PGSs was worse than expected and the best performing PGS for each AG was different from the one reported in the “PGS Catalog” across all AGs.
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spelling pubmed-105963422023-10-25 Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries Regazzi, L Bolli, A Cadeddu, C Boccia, S Busby, G Eur J Public Health Parallel Programme BACKGROUND: Polygenic scores (PGS) for coronary artery disease (CAD) measure a person's genetic liability for CAD. PGSs for CAD are generally considered sufficiently predictive in individuals of European ancestry, but their performance is attenuated in non-European ancestry groups (AGs). We collated publicly available CAD PGS and benchmarked their performance across several AGs to evaluate their utility for personalized prevention. METHODS: We queried the “PGS Catalog” to extract standardized odds/hazard ratios (OR/HR) for published CAD PGSs across multiple AGs (European-EUR, African-AFR, Hispanic-HIS, South-Asian-SAS, East-Asian-EAS). We restricted our analysis to PGSs specifically developed for prevalent and/or incident CAD and identified the five best-performing PGSs in each AG. We then computed these PGSs in a sample of 504,096 individuals of EUR (94.5%), AFR (2.6%), SAS (1.9%), EAS (0.7%) and HIS (0.3%) AG and evaluated their performance through logistic regression (covariates: age, sex, family history of CAD, principal components of AG). RESULTS: PGS000018 performed best in SAS (1.69[1.56-1.83]), EUR (1.62[1.60-1.64]) and EAS (1.45[1.11-1.89]). PGS001780 was the best performing PGS in AFR (1.18[1.04-1.33], on par with PGS000749) and ranked second in EUR (1.59[1.57-1.61]) and SAS (1.64[1.53-1.76]). Finally, PGS002262 was best in HIS (1.39[1.07-1.81], almost on par with PGS000337) and second in EASs (1.41[1.13-1.75]). Overall, the highest standardized ORs were found for the SAS and the EUR AGs, while the AFR AG had the worst performances. PGSs performed differently than previously reported both in an absolute and relative way, corroborating the need of a standardized comparison. CONCLUSIONS: There is currently no gold-standard trans-ancestry CAD PGS, but the employment of different AG-specific CAD PGSs can achieve the best possible predictive performance in every individual, an essential prerequisite towards implementing PGSs in CAD personalized prevention protocols. KEY MESSAGES: • No gold standard PGS for CAD exists that can be applied with equal predictive performance across all AGs, which can be partially counterbalance by using the best performing PGS in each AG. • In our analysis, the absolute performance of all PGSs was worse than expected and the best performing PGS for each AG was different from the one reported in the “PGS Catalog” across all AGs. Oxford University Press 2023-10-24 /pmc/articles/PMC10596342/ http://dx.doi.org/10.1093/eurpub/ckad160.222 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Public Health Association. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Parallel Programme
Regazzi, L
Bolli, A
Cadeddu, C
Boccia, S
Busby, G
Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title_full Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title_fullStr Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title_full_unstemmed Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title_short Predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
title_sort predictive performance of polygenic scores for coronary artery disease in multiple genetic ancestries
topic Parallel Programme
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596342/
http://dx.doi.org/10.1093/eurpub/ckad160.222
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