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Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA

BACKGROUND: Studies have demonstrated that the current US guidelines based on American College of Cardiology/American Heart Association (ACC/AHA) Pooled Cohort Equations Risk Calculator may underestimate risk of atherosclerotic cardiovascular disease (CVD) in certain high‐risk individuals, therefore...

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Autores principales: Kakadiaris, Ioannis A., Vrigkas, Michalis, Yen, Albert A., Kuznetsova, Tatiana, Budoff, Matthew, Naghavi, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404456/
https://www.ncbi.nlm.nih.gov/pubmed/30571498
http://dx.doi.org/10.1161/JAHA.118.009476
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author Kakadiaris, Ioannis A.
Vrigkas, Michalis
Yen, Albert A.
Kuznetsova, Tatiana
Budoff, Matthew
Naghavi, Morteza
author_facet Kakadiaris, Ioannis A.
Vrigkas, Michalis
Yen, Albert A.
Kuznetsova, Tatiana
Budoff, Matthew
Naghavi, Morteza
author_sort Kakadiaris, Ioannis A.
collection PubMed
description BACKGROUND: Studies have demonstrated that the current US guidelines based on American College of Cardiology/American Heart Association (ACC/AHA) Pooled Cohort Equations Risk Calculator may underestimate risk of atherosclerotic cardiovascular disease (CVD) in certain high‐risk individuals, therefore missing opportunities for intensive therapy and preventing CVD events. Similarly, the guidelines may overestimate risk in low risk populations resulting in unnecessary statin therapy. We used Machine Learning (ML) to tackle this problem. METHODS AND RESULTS: We developed a ML Risk Calculator based on Support Vector Machines (SVMs) using a 13‐year follow up data set from MESA (the Multi‐Ethnic Study of Atherosclerosis) of 6459 participants who were atherosclerotic CVD‐free at baseline. We provided identical input to both risk calculators and compared their performance. We then used the FLEMENGHO study (the Flemish Study of Environment, Genes and Health Outcomes) to validate the model in an external cohort. ACC/AHA Risk Calculator, based on 7.5% 10‐year risk threshold, recommended statin to 46.0%. Despite this high proportion, 23.8% of the 480 “Hard CVD” events occurred in those not recommended statin, resulting in sensitivity 0.76, specificity 0.56, and AUC 0.71. In contrast, ML Risk Calculator recommended only 11.4% to take statin, and only 14.4% of “Hard CVD” events occurred in those not recommended statin, resulting in sensitivity 0.86, specificity 0.95, and AUC 0.92. Similar results were found for prediction of “All CVD” events. CONCLUSIONS: The ML Risk Calculator outperformed the ACC/AHA Risk Calculator by recommending less drug therapy, yet missing fewer events. Additional studies are underway to validate the ML model in other cohorts and to explore its ability in short‐term CVD risk prediction.
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spelling pubmed-64044562019-03-18 Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA Kakadiaris, Ioannis A. Vrigkas, Michalis Yen, Albert A. Kuznetsova, Tatiana Budoff, Matthew Naghavi, Morteza J Am Heart Assoc Original Research BACKGROUND: Studies have demonstrated that the current US guidelines based on American College of Cardiology/American Heart Association (ACC/AHA) Pooled Cohort Equations Risk Calculator may underestimate risk of atherosclerotic cardiovascular disease (CVD) in certain high‐risk individuals, therefore missing opportunities for intensive therapy and preventing CVD events. Similarly, the guidelines may overestimate risk in low risk populations resulting in unnecessary statin therapy. We used Machine Learning (ML) to tackle this problem. METHODS AND RESULTS: We developed a ML Risk Calculator based on Support Vector Machines (SVMs) using a 13‐year follow up data set from MESA (the Multi‐Ethnic Study of Atherosclerosis) of 6459 participants who were atherosclerotic CVD‐free at baseline. We provided identical input to both risk calculators and compared their performance. We then used the FLEMENGHO study (the Flemish Study of Environment, Genes and Health Outcomes) to validate the model in an external cohort. ACC/AHA Risk Calculator, based on 7.5% 10‐year risk threshold, recommended statin to 46.0%. Despite this high proportion, 23.8% of the 480 “Hard CVD” events occurred in those not recommended statin, resulting in sensitivity 0.76, specificity 0.56, and AUC 0.71. In contrast, ML Risk Calculator recommended only 11.4% to take statin, and only 14.4% of “Hard CVD” events occurred in those not recommended statin, resulting in sensitivity 0.86, specificity 0.95, and AUC 0.92. Similar results were found for prediction of “All CVD” events. CONCLUSIONS: The ML Risk Calculator outperformed the ACC/AHA Risk Calculator by recommending less drug therapy, yet missing fewer events. Additional studies are underway to validate the ML model in other cohorts and to explore its ability in short‐term CVD risk prediction. John Wiley and Sons Inc. 2018-11-11 /pmc/articles/PMC6404456/ /pubmed/30571498 http://dx.doi.org/10.1161/JAHA.118.009476 Text en © 2018 The Authors and University of Houston. 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Kakadiaris, Ioannis A.
Vrigkas, Michalis
Yen, Albert A.
Kuznetsova, Tatiana
Budoff, Matthew
Naghavi, Morteza
Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title_full Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title_fullStr Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title_full_unstemmed Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title_short Machine Learning Outperforms ACC/AHA CVD Risk Calculator in MESA
title_sort machine learning outperforms acc/aha cvd risk calculator in mesa
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404456/
https://www.ncbi.nlm.nih.gov/pubmed/30571498
http://dx.doi.org/10.1161/JAHA.118.009476
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