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Heterogeneity in coronary heart disease risk
There is large inter-individual heterogeneity in risk of coronary heart disease (CHD). Risk factors traditionally used in primary risk assessment only partially explain this heterogeneity. Residual, unobserved heterogeneity leads to age-related attenuation of hazard rates and underestimation of haza...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203574/ https://www.ncbi.nlm.nih.gov/pubmed/35710917 http://dx.doi.org/10.1038/s41598-022-14013-3 |
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author | Simonetto, Cristoforo Rospleszcz, Susanne Kaiser, Jan Christian Furukawa, Kyoji |
author_facet | Simonetto, Cristoforo Rospleszcz, Susanne Kaiser, Jan Christian Furukawa, Kyoji |
author_sort | Simonetto, Cristoforo |
collection | PubMed |
description | There is large inter-individual heterogeneity in risk of coronary heart disease (CHD). Risk factors traditionally used in primary risk assessment only partially explain this heterogeneity. Residual, unobserved heterogeneity leads to age-related attenuation of hazard rates and underestimation of hazard ratios. Its magnitude is unknown. Therefore, we aimed to estimate a lower and an approximate upper bound. Heterogeneity was parametrized by a log-normal distribution with shape parameter σ. Analysis was based on published data. From concordance indices of studies including traditional risk factors and additional diagnostic imaging data, we calculated the part of heterogeneity explained by imaging data. For traditional risk assessment, this part typically remains unexplained, thus constituting a lower bound on unobserved heterogeneity. Next, the potential impact of heterogeneity on CHD hazard rates in several large countries was investigated. CHD rates increase with age but the increase attenuates with age. Presuming this attenuation to be largely caused by heterogeneity, an approximate upper bound on σ was derived. Taking together both bounds, unobserved heterogeneity in studies without imaging information can be described by a shape parameter in the range σ = 1–2. It substantially contributes to observed age-dependences of hazard ratios and may lead to underestimation of hazard ratios by a factor of about two. Therefore, analysis of studies for primary CHD risk assessment should account for unobserved heterogeneity. |
format | Online Article Text |
id | pubmed-9203574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92035742022-06-18 Heterogeneity in coronary heart disease risk Simonetto, Cristoforo Rospleszcz, Susanne Kaiser, Jan Christian Furukawa, Kyoji Sci Rep Article There is large inter-individual heterogeneity in risk of coronary heart disease (CHD). Risk factors traditionally used in primary risk assessment only partially explain this heterogeneity. Residual, unobserved heterogeneity leads to age-related attenuation of hazard rates and underestimation of hazard ratios. Its magnitude is unknown. Therefore, we aimed to estimate a lower and an approximate upper bound. Heterogeneity was parametrized by a log-normal distribution with shape parameter σ. Analysis was based on published data. From concordance indices of studies including traditional risk factors and additional diagnostic imaging data, we calculated the part of heterogeneity explained by imaging data. For traditional risk assessment, this part typically remains unexplained, thus constituting a lower bound on unobserved heterogeneity. Next, the potential impact of heterogeneity on CHD hazard rates in several large countries was investigated. CHD rates increase with age but the increase attenuates with age. Presuming this attenuation to be largely caused by heterogeneity, an approximate upper bound on σ was derived. Taking together both bounds, unobserved heterogeneity in studies without imaging information can be described by a shape parameter in the range σ = 1–2. It substantially contributes to observed age-dependences of hazard ratios and may lead to underestimation of hazard ratios by a factor of about two. Therefore, analysis of studies for primary CHD risk assessment should account for unobserved heterogeneity. Nature Publishing Group UK 2022-06-16 /pmc/articles/PMC9203574/ /pubmed/35710917 http://dx.doi.org/10.1038/s41598-022-14013-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Simonetto, Cristoforo Rospleszcz, Susanne Kaiser, Jan Christian Furukawa, Kyoji Heterogeneity in coronary heart disease risk |
title | Heterogeneity in coronary heart disease risk |
title_full | Heterogeneity in coronary heart disease risk |
title_fullStr | Heterogeneity in coronary heart disease risk |
title_full_unstemmed | Heterogeneity in coronary heart disease risk |
title_short | Heterogeneity in coronary heart disease risk |
title_sort | heterogeneity in coronary heart disease risk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203574/ https://www.ncbi.nlm.nih.gov/pubmed/35710917 http://dx.doi.org/10.1038/s41598-022-14013-3 |
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