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Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction
Given the limited accuracy of clinically used risk scores such as the Systematic COronary Risk Evaluation 2 system and the Second Manifestations of ARTerial disease 2 risk scores, novel risk algorithms determining an individual’s susceptibility of future incident or recurrent atherosclerotic cardiov...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163980/ https://www.ncbi.nlm.nih.gov/pubmed/36988179 http://dx.doi.org/10.1093/eurheartj/ehad161 |
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author | Nurmohamed, Nick S Kraaijenhof, Jordan M Mayr, Manuel Nicholls, Stephen J Koenig, Wolfgang Catapano, Alberico L Stroes, Erik S G |
author_facet | Nurmohamed, Nick S Kraaijenhof, Jordan M Mayr, Manuel Nicholls, Stephen J Koenig, Wolfgang Catapano, Alberico L Stroes, Erik S G |
author_sort | Nurmohamed, Nick S |
collection | PubMed |
description | Given the limited accuracy of clinically used risk scores such as the Systematic COronary Risk Evaluation 2 system and the Second Manifestations of ARTerial disease 2 risk scores, novel risk algorithms determining an individual’s susceptibility of future incident or recurrent atherosclerotic cardiovascular disease (ASCVD) risk are urgently needed. Due to major improvements in assay techniques, multimarker proteomic and lipidomic panels hold the promise to be reliably assessed in a high-throughput routine. Novel machine learning-based approaches have facilitated the use of this high-dimensional data resulting from these analyses for ASCVD risk prediction. More than a dozen of large-scale retrospective studies using different sets of biomarkers and different statistical methods have consistently demonstrated the additive prognostic value of these panels over traditionally used clinical risk scores. Prospective studies are needed to determine the clinical utility of a biomarker panel in clinical ASCVD risk stratification. When combined with the genetic predisposition captured with polygenic risk scores and the actual ASCVD phenotype observed with coronary artery imaging, proteomics and lipidomics can advance understanding of the complex multifactorial causes underlying an individual’s ASCVD risk. |
format | Online Article Text |
id | pubmed-10163980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101639802023-05-07 Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction Nurmohamed, Nick S Kraaijenhof, Jordan M Mayr, Manuel Nicholls, Stephen J Koenig, Wolfgang Catapano, Alberico L Stroes, Erik S G Eur Heart J State of the Art Review Given the limited accuracy of clinically used risk scores such as the Systematic COronary Risk Evaluation 2 system and the Second Manifestations of ARTerial disease 2 risk scores, novel risk algorithms determining an individual’s susceptibility of future incident or recurrent atherosclerotic cardiovascular disease (ASCVD) risk are urgently needed. Due to major improvements in assay techniques, multimarker proteomic and lipidomic panels hold the promise to be reliably assessed in a high-throughput routine. Novel machine learning-based approaches have facilitated the use of this high-dimensional data resulting from these analyses for ASCVD risk prediction. More than a dozen of large-scale retrospective studies using different sets of biomarkers and different statistical methods have consistently demonstrated the additive prognostic value of these panels over traditionally used clinical risk scores. Prospective studies are needed to determine the clinical utility of a biomarker panel in clinical ASCVD risk stratification. When combined with the genetic predisposition captured with polygenic risk scores and the actual ASCVD phenotype observed with coronary artery imaging, proteomics and lipidomics can advance understanding of the complex multifactorial causes underlying an individual’s ASCVD risk. Oxford University Press 2023-03-29 /pmc/articles/PMC10163980/ /pubmed/36988179 http://dx.doi.org/10.1093/eurheartj/ehad161 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. 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 | State of the Art Review Nurmohamed, Nick S Kraaijenhof, Jordan M Mayr, Manuel Nicholls, Stephen J Koenig, Wolfgang Catapano, Alberico L Stroes, Erik S G Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title | Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title_full | Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title_fullStr | Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title_full_unstemmed | Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title_short | Proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
title_sort | proteomics and lipidomics in atherosclerotic cardiovascular disease risk prediction |
topic | State of the Art Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163980/ https://www.ncbi.nlm.nih.gov/pubmed/36988179 http://dx.doi.org/10.1093/eurheartj/ehad161 |
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