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Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease

BACKGROUND: There is a well-established relationship between 12-lead electrocardiogram (ECG) and age and mortality. Furthermore, there is increasing evidence that ECG can be used to predict biological age. However, the utility of biological age from ECG for predicting mortality remains unclear. METH...

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Autores principales: Hirota, Naomi, Suzuki, Shinya, Arita, Takuto, Yagi, Naoharu, Otsuka, Takayuki, Yamashita, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359578/
https://www.ncbi.nlm.nih.gov/pubmed/34380426
http://dx.doi.org/10.1186/s12877-021-02391-8
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author Hirota, Naomi
Suzuki, Shinya
Arita, Takuto
Yagi, Naoharu
Otsuka, Takayuki
Yamashita, Takeshi
author_facet Hirota, Naomi
Suzuki, Shinya
Arita, Takuto
Yagi, Naoharu
Otsuka, Takayuki
Yamashita, Takeshi
author_sort Hirota, Naomi
collection PubMed
description BACKGROUND: There is a well-established relationship between 12-lead electrocardiogram (ECG) and age and mortality. Furthermore, there is increasing evidence that ECG can be used to predict biological age. However, the utility of biological age from ECG for predicting mortality remains unclear. METHODS: This was a single-center cohort study from a cardiology specialized hospital. A total of 19,170 patients registered in this study from February 2010 to March 2018. ECG was analyzed in a final 12,837 patients after excluding those with structural heart disease or with pacing beats, atrial or ventricular tachyarrhythmia, or an indeterminate axis (R axis > 180°) on index ECG. The models for biological age were developed by principal component analysis (BA) and the Klemera and Doubal’s method (not adjusted for age [BA(E)] and adjusted for age [BA(EC)]) using 438 ECG parameters. The predictive capability for all-cause death and cardiovascular death by chronological age (CA) and biological age using the three algorithms were evaluated by receiver operating characteristic analysis. RESULTS: During the mean follow-up period of 320.4 days, there were 55 all-cause deaths and 23 cardiovascular deaths. The predictive capabilities for all-cause death by BA, BA(E), and BA(EC) using area under the curves were 0.731, 0.657, and 0.685, respectively, which were comparable to 0.725 for CA (p = 0.760, 0.141, and 0.308, respectively). The predictive capabilities for cardiovascular death by BA, BA(E), and BA(EC) were 0.682, 0.685, and 0.692, respectively, which were also comparable to 0.674 for CA (p = 0.775, 0.839, and 0.706, respectively). In patients aged 60–74 years old, the area under the curves for all-cause death by BA, BA(E), and BA(EC) were 0.619, 0.702, and 0.697, respectively, which tended to be or were significantly higher than 0.482 for CA (p = 0.064, 0.006, and 0.005, respectively). CONCLUSION: Biological age by 12-lead ECG showed a similar predictive capability for mortality compared to CA among total patients, but partially showed a significant increase in predictive capability among patients aged 60–74 years old. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02391-8.
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spelling pubmed-83595782021-08-16 Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease Hirota, Naomi Suzuki, Shinya Arita, Takuto Yagi, Naoharu Otsuka, Takayuki Yamashita, Takeshi BMC Geriatr Research Article BACKGROUND: There is a well-established relationship between 12-lead electrocardiogram (ECG) and age and mortality. Furthermore, there is increasing evidence that ECG can be used to predict biological age. However, the utility of biological age from ECG for predicting mortality remains unclear. METHODS: This was a single-center cohort study from a cardiology specialized hospital. A total of 19,170 patients registered in this study from February 2010 to March 2018. ECG was analyzed in a final 12,837 patients after excluding those with structural heart disease or with pacing beats, atrial or ventricular tachyarrhythmia, or an indeterminate axis (R axis > 180°) on index ECG. The models for biological age were developed by principal component analysis (BA) and the Klemera and Doubal’s method (not adjusted for age [BA(E)] and adjusted for age [BA(EC)]) using 438 ECG parameters. The predictive capability for all-cause death and cardiovascular death by chronological age (CA) and biological age using the three algorithms were evaluated by receiver operating characteristic analysis. RESULTS: During the mean follow-up period of 320.4 days, there were 55 all-cause deaths and 23 cardiovascular deaths. The predictive capabilities for all-cause death by BA, BA(E), and BA(EC) using area under the curves were 0.731, 0.657, and 0.685, respectively, which were comparable to 0.725 for CA (p = 0.760, 0.141, and 0.308, respectively). The predictive capabilities for cardiovascular death by BA, BA(E), and BA(EC) were 0.682, 0.685, and 0.692, respectively, which were also comparable to 0.674 for CA (p = 0.775, 0.839, and 0.706, respectively). In patients aged 60–74 years old, the area under the curves for all-cause death by BA, BA(E), and BA(EC) were 0.619, 0.702, and 0.697, respectively, which tended to be or were significantly higher than 0.482 for CA (p = 0.064, 0.006, and 0.005, respectively). CONCLUSION: Biological age by 12-lead ECG showed a similar predictive capability for mortality compared to CA among total patients, but partially showed a significant increase in predictive capability among patients aged 60–74 years old. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02391-8. BioMed Central 2021-08-11 /pmc/articles/PMC8359578/ /pubmed/34380426 http://dx.doi.org/10.1186/s12877-021-02391-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Hirota, Naomi
Suzuki, Shinya
Arita, Takuto
Yagi, Naoharu
Otsuka, Takayuki
Yamashita, Takeshi
Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title_full Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title_fullStr Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title_full_unstemmed Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title_short Prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
title_sort prediction of biological age and all-cause mortality by 12-lead electrocardiogram in patients without structural heart disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359578/
https://www.ncbi.nlm.nih.gov/pubmed/34380426
http://dx.doi.org/10.1186/s12877-021-02391-8
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