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Cardiac injury is associated with inflammation in geriatric COVID‐19 patients
BACKGROUND: Geriatric patients with coronavirus disease (COVID‐19) are at high risk of developing cardiac injury. Identifying the factors that affect high‐sensitivity cardiac troponin I may indicate the cause of cardiac injury in elderly patients, and this could hopefully assist in protecting heart...
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/PMC7744922/ https://www.ncbi.nlm.nih.gov/pubmed/33210392 http://dx.doi.org/10.1002/jcla.23654 |
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author | Yan, Xu Wang, Shuang Ma, Piyong Yang, Bo Si, Daoyuan Liu, Guohui Liu, Long Ding, Mei Yang, Wen Li, Jiayu Sun, Huan Yang, Ping |
author_facet | Yan, Xu Wang, Shuang Ma, Piyong Yang, Bo Si, Daoyuan Liu, Guohui Liu, Long Ding, Mei Yang, Wen Li, Jiayu Sun, Huan Yang, Ping |
author_sort | Yan, Xu |
collection | PubMed |
description | BACKGROUND: Geriatric patients with coronavirus disease (COVID‐19) are at high risk of developing cardiac injury. Identifying the factors that affect high‐sensitivity cardiac troponin I may indicate the cause of cardiac injury in elderly patients, and this could hopefully assist in protecting heart function in this patient population. METHODS: One hundred and eighty inpatients who were admitted for COVID‐19 were screened. Patients older than 60 years were included in this study, and the clinical characteristics and laboratory results of the cohort were analyzed. The correlation between cardiac injury and clinical/laboratory variables was statistically analyzed, and further logistic regression was performed to determine how these variables influence cardiac injury in geriatric patients. RESULTS: Age (p < 0.001) significantly correlated with cardiac injury, whereas sex (p = 0.372) and coexisting diseases did not. Rising procalcitonin (p = 0.001), interleukin‐2 receptor (p < 0.001), interleukin 6 (p = 0.001), interleukin 10 (p < 0.001), tumor necrosis factor α (p = 0.001), high‐sensitivity C‐reactive protein (p = 0.001), D‐dimer (p < 0.001), white blood cells (p < 0.001), neutrophils (p = 0.001), declining lymphocytes (p < 0.001), and natural killer cells (p = 0.005) were associated with cardiac injury and showed predictive ability in the multivariate logistic regression. CONCLUSION: Our results suggest that age and inflammatory factors influence cardiac injury in elderly patients. Interfering with inflammation in this patient population may potentially confer cardiac protection. |
format | Online Article Text |
id | pubmed-7744922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77449222020-12-17 Cardiac injury is associated with inflammation in geriatric COVID‐19 patients Yan, Xu Wang, Shuang Ma, Piyong Yang, Bo Si, Daoyuan Liu, Guohui Liu, Long Ding, Mei Yang, Wen Li, Jiayu Sun, Huan Yang, Ping J Clin Lab Anal Research Articles BACKGROUND: Geriatric patients with coronavirus disease (COVID‐19) are at high risk of developing cardiac injury. Identifying the factors that affect high‐sensitivity cardiac troponin I may indicate the cause of cardiac injury in elderly patients, and this could hopefully assist in protecting heart function in this patient population. METHODS: One hundred and eighty inpatients who were admitted for COVID‐19 were screened. Patients older than 60 years were included in this study, and the clinical characteristics and laboratory results of the cohort were analyzed. The correlation between cardiac injury and clinical/laboratory variables was statistically analyzed, and further logistic regression was performed to determine how these variables influence cardiac injury in geriatric patients. RESULTS: Age (p < 0.001) significantly correlated with cardiac injury, whereas sex (p = 0.372) and coexisting diseases did not. Rising procalcitonin (p = 0.001), interleukin‐2 receptor (p < 0.001), interleukin 6 (p = 0.001), interleukin 10 (p < 0.001), tumor necrosis factor α (p = 0.001), high‐sensitivity C‐reactive protein (p = 0.001), D‐dimer (p < 0.001), white blood cells (p < 0.001), neutrophils (p = 0.001), declining lymphocytes (p < 0.001), and natural killer cells (p = 0.005) were associated with cardiac injury and showed predictive ability in the multivariate logistic regression. CONCLUSION: Our results suggest that age and inflammatory factors influence cardiac injury in elderly patients. Interfering with inflammation in this patient population may potentially confer cardiac protection. John Wiley and Sons Inc. 2020-11-18 /pmc/articles/PMC7744922/ /pubmed/33210392 http://dx.doi.org/10.1002/jcla.23654 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis 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 | Research Articles Yan, Xu Wang, Shuang Ma, Piyong Yang, Bo Si, Daoyuan Liu, Guohui Liu, Long Ding, Mei Yang, Wen Li, Jiayu Sun, Huan Yang, Ping Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title | Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title_full | Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title_fullStr | Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title_full_unstemmed | Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title_short | Cardiac injury is associated with inflammation in geriatric COVID‐19 patients |
title_sort | cardiac injury is associated with inflammation in geriatric covid‐19 patients |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744922/ https://www.ncbi.nlm.nih.gov/pubmed/33210392 http://dx.doi.org/10.1002/jcla.23654 |
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