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Adding multiple risk factors improves Framingham coronary heart disease risk scores

PURPOSE: Since the introduction of the Framingham Risk Score (FRS), numerous versions of coronary heart disease (CHD) prediction models have claimed improvement over the FRS. Tzoulaki et al challenged the validity of these claims by illustrating methodology deficiencies among the studies. However, t...

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Autores principales: Hu, Guizhou, Root, Martin, Duncan, Ashlee W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162681/
https://www.ncbi.nlm.nih.gov/pubmed/25228812
http://dx.doi.org/10.2147/VHRM.S69672
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author Hu, Guizhou
Root, Martin
Duncan, Ashlee W
author_facet Hu, Guizhou
Root, Martin
Duncan, Ashlee W
author_sort Hu, Guizhou
collection PubMed
description PURPOSE: Since the introduction of the Framingham Risk Score (FRS), numerous versions of coronary heart disease (CHD) prediction models have claimed improvement over the FRS. Tzoulaki et al challenged the validity of these claims by illustrating methodology deficiencies among the studies. However, the question remains: Is it possible to create a new CHD model that is better than FRS while overcoming the noted deficiencies? To address this, a new CHD prediction model was developed by integrating additional risk factors, using a novel modeling process. METHODS: Using the National Health Nutritional Examination Survey III data set with CHD-specific mortality outcomes and the Atherosclerosis Risk in Communities data set with CHD incidence outcomes, two FRSs (FRSv1 from 1998 and FRSv2 from National Cholesterol Education Program Adult Treatment Panel III), along with an additional risk score in which the high density lipoprotein (HDL) component of FRSv1 was ignored (FRSHDL), were compared with a new CHD model (NEW-CHD). This new model contains seven elements: the original Framingham equation, FRSv1, and six additional risk factors. Discrimination, calibration, and reclassification improvements all were assessed among models. RESULTS: Discrimination was improved for NEW-CHD in both cohorts when compared with FRSv1 and FRSv2 (P<0.05) and was similar in magnitude to the improvement of FRSv1 over FRSHDL. NEW-CHD had a similar calibration to FRSv2 and was improved over FRSv1. Net reclassification for NEW-CHD was substantially improved over both FRSv1 and FRSv2, for both cohorts, and was similar in magnitude to the improvement of FRSv1 over FRSHDL. CONCLUSION: While overcoming several methodology deficiencies reported by earlier authors, the NEW-CHD model improved CHD risk assessment when compared with the FRSs, comparable to the improvement of adding HDL to the FRS.
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spelling pubmed-41626812014-09-16 Adding multiple risk factors improves Framingham coronary heart disease risk scores Hu, Guizhou Root, Martin Duncan, Ashlee W Vasc Health Risk Manag Original Research PURPOSE: Since the introduction of the Framingham Risk Score (FRS), numerous versions of coronary heart disease (CHD) prediction models have claimed improvement over the FRS. Tzoulaki et al challenged the validity of these claims by illustrating methodology deficiencies among the studies. However, the question remains: Is it possible to create a new CHD model that is better than FRS while overcoming the noted deficiencies? To address this, a new CHD prediction model was developed by integrating additional risk factors, using a novel modeling process. METHODS: Using the National Health Nutritional Examination Survey III data set with CHD-specific mortality outcomes and the Atherosclerosis Risk in Communities data set with CHD incidence outcomes, two FRSs (FRSv1 from 1998 and FRSv2 from National Cholesterol Education Program Adult Treatment Panel III), along with an additional risk score in which the high density lipoprotein (HDL) component of FRSv1 was ignored (FRSHDL), were compared with a new CHD model (NEW-CHD). This new model contains seven elements: the original Framingham equation, FRSv1, and six additional risk factors. Discrimination, calibration, and reclassification improvements all were assessed among models. RESULTS: Discrimination was improved for NEW-CHD in both cohorts when compared with FRSv1 and FRSv2 (P<0.05) and was similar in magnitude to the improvement of FRSv1 over FRSHDL. NEW-CHD had a similar calibration to FRSv2 and was improved over FRSv1. Net reclassification for NEW-CHD was substantially improved over both FRSv1 and FRSv2, for both cohorts, and was similar in magnitude to the improvement of FRSv1 over FRSHDL. CONCLUSION: While overcoming several methodology deficiencies reported by earlier authors, the NEW-CHD model improved CHD risk assessment when compared with the FRSs, comparable to the improvement of adding HDL to the FRS. Dove Medical Press 2014-09-05 /pmc/articles/PMC4162681/ /pubmed/25228812 http://dx.doi.org/10.2147/VHRM.S69672 Text en © 2014 Hu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Hu, Guizhou
Root, Martin
Duncan, Ashlee W
Adding multiple risk factors improves Framingham coronary heart disease risk scores
title Adding multiple risk factors improves Framingham coronary heart disease risk scores
title_full Adding multiple risk factors improves Framingham coronary heart disease risk scores
title_fullStr Adding multiple risk factors improves Framingham coronary heart disease risk scores
title_full_unstemmed Adding multiple risk factors improves Framingham coronary heart disease risk scores
title_short Adding multiple risk factors improves Framingham coronary heart disease risk scores
title_sort adding multiple risk factors improves framingham coronary heart disease risk scores
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162681/
https://www.ncbi.nlm.nih.gov/pubmed/25228812
http://dx.doi.org/10.2147/VHRM.S69672
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