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Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis
BACKGROUND: Many indices of heart rate variability (HRV) and heart rate dynamics have been proposed as cardiovascular mortality risk predictors, but the redundancy between their predictive powers is unknown. METHODS: From the Allostatic State Mapping by Ambulatory ECG Repository project database, 24...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816809/ https://www.ncbi.nlm.nih.gov/pubmed/33263196 http://dx.doi.org/10.1111/anec.12790 |
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author | Yuda, Emi Ueda, Norihiro Kisohara, Masaya Hayano, Junichiro |
author_facet | Yuda, Emi Ueda, Norihiro Kisohara, Masaya Hayano, Junichiro |
author_sort | Yuda, Emi |
collection | PubMed |
description | BACKGROUND: Many indices of heart rate variability (HRV) and heart rate dynamics have been proposed as cardiovascular mortality risk predictors, but the redundancy between their predictive powers is unknown. METHODS: From the Allostatic State Mapping by Ambulatory ECG Repository project database, 24‐hr ECG data showing continuous sinus rhythm were extracted and SD of normal‐to‐normal R‐R interval (SDNN), very‐low‐frequency power (VLF), scaling exponent α(1), deceleration capacity (DC), and non‐Gaussianity λ(25s) were calculated. The values were dichotomized into high‐risk and low‐risk values using the cutoffs reported in previous studies to predict mortality after acute myocardial infarction. The rate of multiple high‐risk predictors accumulating in the same person was examined and was compared with the rate expected under the assumption that these predictors are independent of each other. RESULTS: Among 265,291 ECG data from the ALLSTAR database, the rates of subjects with high‐risk SDNN, DC, VLF, α(1), and λ(25s) values were 2.95, 2.75, 5.89, 15.75, and 18.82%, respectively. The observed rate of subjects without any high‐risk value was 66.68%, which was 1.10 times the expected rate (60.74%). The ratios of observed rate to the expected rate at which one, two, three, four, and five high‐risk values accumulate in the same person were 0.73 times (24.10 and 32.82%), 1.10 times (6.56 and 5.99%), 4.26 times (1.87 and 0.44%), 47.66 times (0.63 and 0.013%), and 1,140.66 times (0.16 and 0.00014%), respectively. CONCLUSIONS: High‐risk predictors of HRV and heart rate dynamics tend to cluster in the same person, indicating a high degree of redundancy between them. |
format | Online Article Text |
id | pubmed-7816809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78168092021-01-27 Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis Yuda, Emi Ueda, Norihiro Kisohara, Masaya Hayano, Junichiro Ann Noninvasive Electrocardiol Original Articles BACKGROUND: Many indices of heart rate variability (HRV) and heart rate dynamics have been proposed as cardiovascular mortality risk predictors, but the redundancy between their predictive powers is unknown. METHODS: From the Allostatic State Mapping by Ambulatory ECG Repository project database, 24‐hr ECG data showing continuous sinus rhythm were extracted and SD of normal‐to‐normal R‐R interval (SDNN), very‐low‐frequency power (VLF), scaling exponent α(1), deceleration capacity (DC), and non‐Gaussianity λ(25s) were calculated. The values were dichotomized into high‐risk and low‐risk values using the cutoffs reported in previous studies to predict mortality after acute myocardial infarction. The rate of multiple high‐risk predictors accumulating in the same person was examined and was compared with the rate expected under the assumption that these predictors are independent of each other. RESULTS: Among 265,291 ECG data from the ALLSTAR database, the rates of subjects with high‐risk SDNN, DC, VLF, α(1), and λ(25s) values were 2.95, 2.75, 5.89, 15.75, and 18.82%, respectively. The observed rate of subjects without any high‐risk value was 66.68%, which was 1.10 times the expected rate (60.74%). The ratios of observed rate to the expected rate at which one, two, three, four, and five high‐risk values accumulate in the same person were 0.73 times (24.10 and 32.82%), 1.10 times (6.56 and 5.99%), 4.26 times (1.87 and 0.44%), 47.66 times (0.63 and 0.013%), and 1,140.66 times (0.16 and 0.00014%), respectively. CONCLUSIONS: High‐risk predictors of HRV and heart rate dynamics tend to cluster in the same person, indicating a high degree of redundancy between them. John Wiley and Sons Inc. 2020-08-17 /pmc/articles/PMC7816809/ /pubmed/33263196 http://dx.doi.org/10.1111/anec.12790 Text en © 2020 The Authors. Annals of Noninvasive Electrocardiology published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Yuda, Emi Ueda, Norihiro Kisohara, Masaya Hayano, Junichiro Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title | Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title_full | Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title_fullStr | Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title_full_unstemmed | Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title_short | Redundancy among risk predictors derived from heart rate variability and dynamics: ALLSTAR big data analysis |
title_sort | redundancy among risk predictors derived from heart rate variability and dynamics: allstar big data analysis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816809/ https://www.ncbi.nlm.nih.gov/pubmed/33263196 http://dx.doi.org/10.1111/anec.12790 |
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