Cargando…

Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study

The predictive ability of coronary heart disease (CHD) and ischemic stroke (IS) polygenic risk scores (PRS) have been evaluated individually, but whether they predict the combined outcome of atherosclerotic cardiovascular disease (ASCVD) remains insufficiently researched. It is also unclear whether...

Descripción completa

Detalles Bibliográficos
Autores principales: Bebo, Allison, Jarmul, Jamie A., Pletcher, Mark J., Hasbani, Natalie R., Couper, David, Nambi, Vijay, Ballantyne, Christie M., Fornage, Myriam, Morrison, Alanna C., Avery, Christy L., de Vries, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275447/
https://www.ncbi.nlm.nih.gov/pubmed/37327218
http://dx.doi.org/10.1371/journal.pone.0285259
_version_ 1785059875315777536
author Bebo, Allison
Jarmul, Jamie A.
Pletcher, Mark J.
Hasbani, Natalie R.
Couper, David
Nambi, Vijay
Ballantyne, Christie M.
Fornage, Myriam
Morrison, Alanna C.
Avery, Christy L.
de Vries, Paul S.
author_facet Bebo, Allison
Jarmul, Jamie A.
Pletcher, Mark J.
Hasbani, Natalie R.
Couper, David
Nambi, Vijay
Ballantyne, Christie M.
Fornage, Myriam
Morrison, Alanna C.
Avery, Christy L.
de Vries, Paul S.
author_sort Bebo, Allison
collection PubMed
description The predictive ability of coronary heart disease (CHD) and ischemic stroke (IS) polygenic risk scores (PRS) have been evaluated individually, but whether they predict the combined outcome of atherosclerotic cardiovascular disease (ASCVD) remains insufficiently researched. It is also unclear whether associations of the CHD and IS PRS with ASCVD are independent of subclinical atherosclerosis measures. 7,286 White and 2,016 Black participants from the population-based Atherosclerosis Risk in Communities study who were free of cardiovascular disease and type 2 diabetes at baseline were included. We computed previously validated CHD and IS PRS consisting of 1,745,179 and 3,225,583 genetic variants, respectively. Cox proportional hazards models were used to test the association between each PRS and ASCVD, adjusting for traditional risk factors, ankle-brachial index, carotid intima media thickness, and carotid plaque. The hazard ratios (HR) for the CHD and IS PRS were significant with HR of 1.50 (95% CI: 1.36–1.66) and 1.31 (95% CI: 1.18–1.45) respectively for the risk of incident ASCVD per standard deviation increase in CHD and IS PRS among White participants after adjusting for traditional risk factors. The HR for the CHD PRS was not significant with an HR of 0.95 (95% CI: 0.79–1.13) for the risk of incident ASCVD in Black participants. The HR for the IS PRS was significant with an HR of 1.26 (95%CI: 1.05–1.51) for the risk of incident ASCVD in Black participants. The association of the CHD and IS PRS with ASCVD was not attenuated in White participants after adjustment for ankle-brachial index, carotid intima media thickness, and carotid plaque. The CHD and IS PRS do not cross-predict well, and predict better the outcome for which they were created than the composite ASCVD outcome. Thus, the use of the composite outcome of ASCVD may not be ideal for genetic risk prediction.
format Online
Article
Text
id pubmed-10275447
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-102754472023-06-17 Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study Bebo, Allison Jarmul, Jamie A. Pletcher, Mark J. Hasbani, Natalie R. Couper, David Nambi, Vijay Ballantyne, Christie M. Fornage, Myriam Morrison, Alanna C. Avery, Christy L. de Vries, Paul S. PLoS One Research Article The predictive ability of coronary heart disease (CHD) and ischemic stroke (IS) polygenic risk scores (PRS) have been evaluated individually, but whether they predict the combined outcome of atherosclerotic cardiovascular disease (ASCVD) remains insufficiently researched. It is also unclear whether associations of the CHD and IS PRS with ASCVD are independent of subclinical atherosclerosis measures. 7,286 White and 2,016 Black participants from the population-based Atherosclerosis Risk in Communities study who were free of cardiovascular disease and type 2 diabetes at baseline were included. We computed previously validated CHD and IS PRS consisting of 1,745,179 and 3,225,583 genetic variants, respectively. Cox proportional hazards models were used to test the association between each PRS and ASCVD, adjusting for traditional risk factors, ankle-brachial index, carotid intima media thickness, and carotid plaque. The hazard ratios (HR) for the CHD and IS PRS were significant with HR of 1.50 (95% CI: 1.36–1.66) and 1.31 (95% CI: 1.18–1.45) respectively for the risk of incident ASCVD per standard deviation increase in CHD and IS PRS among White participants after adjusting for traditional risk factors. The HR for the CHD PRS was not significant with an HR of 0.95 (95% CI: 0.79–1.13) for the risk of incident ASCVD in Black participants. The HR for the IS PRS was significant with an HR of 1.26 (95%CI: 1.05–1.51) for the risk of incident ASCVD in Black participants. The association of the CHD and IS PRS with ASCVD was not attenuated in White participants after adjustment for ankle-brachial index, carotid intima media thickness, and carotid plaque. The CHD and IS PRS do not cross-predict well, and predict better the outcome for which they were created than the composite ASCVD outcome. Thus, the use of the composite outcome of ASCVD may not be ideal for genetic risk prediction. Public Library of Science 2023-06-16 /pmc/articles/PMC10275447/ /pubmed/37327218 http://dx.doi.org/10.1371/journal.pone.0285259 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Bebo, Allison
Jarmul, Jamie A.
Pletcher, Mark J.
Hasbani, Natalie R.
Couper, David
Nambi, Vijay
Ballantyne, Christie M.
Fornage, Myriam
Morrison, Alanna C.
Avery, Christy L.
de Vries, Paul S.
Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title_full Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title_fullStr Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title_full_unstemmed Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title_short Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
title_sort coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275447/
https://www.ncbi.nlm.nih.gov/pubmed/37327218
http://dx.doi.org/10.1371/journal.pone.0285259
work_keys_str_mv AT beboallison coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT jarmuljamiea coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT pletchermarkj coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT hasbaninatalier coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT couperdavid coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT nambivijay coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT ballantynechristiem coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT fornagemyriam coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT morrisonalannac coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT averychristyl coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy
AT devriespauls coronaryheartdiseaseandischemicstrokepolygenicriskscoresandatheroscleroticcardiovasculardiseaseinadiversepopulationbasedcohortstudy