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Novel Self‐Report Tool for Cardiovascular Risk Assessment
BACKGROUND: The currently used atherosclerotic cardiovascular disease risk calculator relies on several measured variables and does not incorporate some well‐established risk factors such as family history of premature myocardial infarction and other nontraditional risk factors. Our study aimed to d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951080/ https://www.ncbi.nlm.nih.gov/pubmed/31818214 http://dx.doi.org/10.1161/JAHA.119.014123 |
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author | Mansoor, Hend Jo, Ara Beau De Rochars, V. Madsen Pepine, Carl J. Mainous, Arch G. |
author_facet | Mansoor, Hend Jo, Ara Beau De Rochars, V. Madsen Pepine, Carl J. Mainous, Arch G. |
author_sort | Mansoor, Hend |
collection | PubMed |
description | BACKGROUND: The currently used atherosclerotic cardiovascular disease risk calculator relies on several measured variables and does not incorporate some well‐established risk factors such as family history of premature myocardial infarction and other nontraditional risk factors. Our study aimed to develop and validate a simple risk score to predict 10‐year risk of incident cardiovascular events using patient‐reported information. METHODS AND RESULTS: Using data from the Atherosclerosis Risk in Communities cohort, we identified adults with no previous history of cardiovascular disease and randomly divided the cohort into “development” (70%) and “validation” (30%) subgroups. Adjusted Cox regression modeling was used to develop a prediction model. The predictive performance of the new risk score was compared with the score derived from the atherosclerotic cardiovascular disease risk calculator. A total of 9285 individuals met the inclusion criteria. During follow‐up (median 8.93 years), a total of 694 (7.47%) incident cardiovascular events occurred. The following 6 factors were included: male sex, age, current smoking, diabetes mellitus, hypertension, and family history of premature myocardial infarction. The C‐statistic was 0.72 in the validation cohort with good calibration. The area under the curve for the simple risk score was comparable to the atherosclerotic cardiovascular disease risk score. CONCLUSIONS: The novel simple risk score is an easy‐to‐use tool to predict cardiovascular events in adults from self‐reported information without need for laboratory or physical examination data. This risk score included 6‐items and had comparable predictive performance to the guideline recommended atherosclerotic cardiovascular disease risk score but relies solely on self‐reported information. |
format | Online Article Text |
id | pubmed-6951080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69510802020-01-10 Novel Self‐Report Tool for Cardiovascular Risk Assessment Mansoor, Hend Jo, Ara Beau De Rochars, V. Madsen Pepine, Carl J. Mainous, Arch G. J Am Heart Assoc Original Research BACKGROUND: The currently used atherosclerotic cardiovascular disease risk calculator relies on several measured variables and does not incorporate some well‐established risk factors such as family history of premature myocardial infarction and other nontraditional risk factors. Our study aimed to develop and validate a simple risk score to predict 10‐year risk of incident cardiovascular events using patient‐reported information. METHODS AND RESULTS: Using data from the Atherosclerosis Risk in Communities cohort, we identified adults with no previous history of cardiovascular disease and randomly divided the cohort into “development” (70%) and “validation” (30%) subgroups. Adjusted Cox regression modeling was used to develop a prediction model. The predictive performance of the new risk score was compared with the score derived from the atherosclerotic cardiovascular disease risk calculator. A total of 9285 individuals met the inclusion criteria. During follow‐up (median 8.93 years), a total of 694 (7.47%) incident cardiovascular events occurred. The following 6 factors were included: male sex, age, current smoking, diabetes mellitus, hypertension, and family history of premature myocardial infarction. The C‐statistic was 0.72 in the validation cohort with good calibration. The area under the curve for the simple risk score was comparable to the atherosclerotic cardiovascular disease risk score. CONCLUSIONS: The novel simple risk score is an easy‐to‐use tool to predict cardiovascular events in adults from self‐reported information without need for laboratory or physical examination data. This risk score included 6‐items and had comparable predictive performance to the guideline recommended atherosclerotic cardiovascular disease risk score but relies solely on self‐reported information. John Wiley and Sons Inc. 2019-12-10 /pmc/articles/PMC6951080/ /pubmed/31818214 http://dx.doi.org/10.1161/JAHA.119.014123 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Mansoor, Hend Jo, Ara Beau De Rochars, V. Madsen Pepine, Carl J. Mainous, Arch G. Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title | Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title_full | Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title_fullStr | Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title_full_unstemmed | Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title_short | Novel Self‐Report Tool for Cardiovascular Risk Assessment |
title_sort | novel self‐report tool for cardiovascular risk assessment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951080/ https://www.ncbi.nlm.nih.gov/pubmed/31818214 http://dx.doi.org/10.1161/JAHA.119.014123 |
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