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Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality

BACKGROUND: Elevated long‐term systolic blood pressure and resting heart rate (RHR) variability are suggested to amplify the risk of all‐cause mortality (ACM). However, the link between increased RHR and pulse pressure for ACM remained unclear. METHODS AND RESULTS: This study analyzed 46 751 individ...

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Autores principales: Yang, Xiaolei, Hidru, Tesfaldet Habtemariam, Han, Xu, Zhang, Xinyuan, Liu, Yang, Wang, Binhao, Li, Huihua, Wu, Shouling, Xia, Yun‐Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335531/
https://www.ncbi.nlm.nih.gov/pubmed/32174212
http://dx.doi.org/10.1161/JAHA.119.014122
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author Yang, Xiaolei
Hidru, Tesfaldet Habtemariam
Han, Xu
Zhang, Xinyuan
Liu, Yang
Wang, Binhao
Li, Huihua
Wu, Shouling
Xia, Yun‐Long
author_facet Yang, Xiaolei
Hidru, Tesfaldet Habtemariam
Han, Xu
Zhang, Xinyuan
Liu, Yang
Wang, Binhao
Li, Huihua
Wu, Shouling
Xia, Yun‐Long
author_sort Yang, Xiaolei
collection PubMed
description BACKGROUND: Elevated long‐term systolic blood pressure and resting heart rate (RHR) variability are suggested to amplify the risk of all‐cause mortality (ACM). However, the link between increased RHR and pulse pressure for ACM remained unclear. METHODS AND RESULTS: This study analyzed 46 751 individuals from Kailuan Cohort Study for the end outcome of ACM. A Cox regression model was used to estimate hazard ratios for death events. Kaplan‐Meier analysis was performed to study the differences in survival as stratified by the SD, coefficient of variation, and average real variability of RHR and pulse pressure quartiles. A total of 1667 deaths (<65 years of age=866/40351, ≥65 years of age=801/6400) were recorded over 4.97±0.69 years follow‐up. Participants under the age of 65 years in the third and fourth quartiles of pulse pressure SD had an independent increase in risk for ACM (hazard ratio [95% CI], 1.16 [1.06–1.28]; and 1.19 [1.05–1.35], respectively). Additionally, participants >65 years of age had a higher risk for ACM across quartiles of RHR‐SD. The hazard ratio (95% CI) for the subjects in quartiles 2, 3, and 4 were 1.81 (1.10–2.97), 2.31 (1.37–1.3.90), and 2.64 (1.63–4.29), respectively. CONCLUSIONS: An elevated long‐term RHR variability combined with an increased pulse pressure variability or vice versa amplifies the risk of ACM.
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spelling pubmed-73355312020-07-08 Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality Yang, Xiaolei Hidru, Tesfaldet Habtemariam Han, Xu Zhang, Xinyuan Liu, Yang Wang, Binhao Li, Huihua Wu, Shouling Xia, Yun‐Long J Am Heart Assoc Original Research BACKGROUND: Elevated long‐term systolic blood pressure and resting heart rate (RHR) variability are suggested to amplify the risk of all‐cause mortality (ACM). However, the link between increased RHR and pulse pressure for ACM remained unclear. METHODS AND RESULTS: This study analyzed 46 751 individuals from Kailuan Cohort Study for the end outcome of ACM. A Cox regression model was used to estimate hazard ratios for death events. Kaplan‐Meier analysis was performed to study the differences in survival as stratified by the SD, coefficient of variation, and average real variability of RHR and pulse pressure quartiles. A total of 1667 deaths (<65 years of age=866/40351, ≥65 years of age=801/6400) were recorded over 4.97±0.69 years follow‐up. Participants under the age of 65 years in the third and fourth quartiles of pulse pressure SD had an independent increase in risk for ACM (hazard ratio [95% CI], 1.16 [1.06–1.28]; and 1.19 [1.05–1.35], respectively). Additionally, participants >65 years of age had a higher risk for ACM across quartiles of RHR‐SD. The hazard ratio (95% CI) for the subjects in quartiles 2, 3, and 4 were 1.81 (1.10–2.97), 2.31 (1.37–1.3.90), and 2.64 (1.63–4.29), respectively. CONCLUSIONS: An elevated long‐term RHR variability combined with an increased pulse pressure variability or vice versa amplifies the risk of ACM. John Wiley and Sons Inc. 2020-03-16 /pmc/articles/PMC7335531/ /pubmed/32174212 http://dx.doi.org/10.1161/JAHA.119.014122 Text en © 2020 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
Yang, Xiaolei
Hidru, Tesfaldet Habtemariam
Han, Xu
Zhang, Xinyuan
Liu, Yang
Wang, Binhao
Li, Huihua
Wu, Shouling
Xia, Yun‐Long
Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title_full Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title_fullStr Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title_full_unstemmed Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title_short Link Between Elevated Long‐Term Resting Heart Rate Variability and Pulse Pressure Variability for All‐Cause Mortality
title_sort link between elevated long‐term resting heart rate variability and pulse pressure variability for all‐cause mortality
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335531/
https://www.ncbi.nlm.nih.gov/pubmed/32174212
http://dx.doi.org/10.1161/JAHA.119.014122
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