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Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study
Identifying prognostic factors by affordable tools is crucial for guiding gastric cancer (GC) treatments especially at earlier stages for timing interventions. The autonomic function that is clinically assessed by heart rate variability (HRV) is involved in tumorigenesis. This pilot study was aimed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761171/ https://www.ncbi.nlm.nih.gov/pubmed/31554856 http://dx.doi.org/10.1038/s41598-019-50358-y |
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author | Shi, Bo Wang, Lili Yan, Chang Chen, Deli Liu, Mulin Li, Peng |
author_facet | Shi, Bo Wang, Lili Yan, Chang Chen, Deli Liu, Mulin Li, Peng |
author_sort | Shi, Bo |
collection | PubMed |
description | Identifying prognostic factors by affordable tools is crucial for guiding gastric cancer (GC) treatments especially at earlier stages for timing interventions. The autonomic function that is clinically assessed by heart rate variability (HRV) is involved in tumorigenesis. This pilot study was aimed to examine whether nonlinear indices of HRV can be biomarkers of GC severity. Sixty-one newly-diagnosed GC patients were enrolled. Presurgical serum fibrinogen (FIB), carcinoembryonic antigen (CEA), and carbohydrate antigen 19-9 (CA199) were examined. Resting electrocardiogram (ECG) of 5-min was collected prior to surgical treatments to enable the HRV analysis. Twelve nonlinear HRV indices covering the irregularity, complexity, asymmetry, and temporal correlation of heartbeat fluctuations were obtained. Increased short-range temporal correlations, decreased asymmetry, and increased irregularity of heartbeat fluctuations were associated with higher FIB level. Increased irregularity and decreased complexity were also associated with higher CEA level. These associations were independent of age, sex, BMI, alcohol consumption, history of diabetes, left ventricular ejection fraction, and anemia. The results support the hypothesis that perturbations in nonlinear dynamical patterns of HRV predict increased GC severity. Replication in larger samples as well as the examination of longitudinal associations of HRV nonlinear features with cancer prognosis/survival are warranted. |
format | Online Article Text |
id | pubmed-6761171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67611712019-11-12 Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study Shi, Bo Wang, Lili Yan, Chang Chen, Deli Liu, Mulin Li, Peng Sci Rep Article Identifying prognostic factors by affordable tools is crucial for guiding gastric cancer (GC) treatments especially at earlier stages for timing interventions. The autonomic function that is clinically assessed by heart rate variability (HRV) is involved in tumorigenesis. This pilot study was aimed to examine whether nonlinear indices of HRV can be biomarkers of GC severity. Sixty-one newly-diagnosed GC patients were enrolled. Presurgical serum fibrinogen (FIB), carcinoembryonic antigen (CEA), and carbohydrate antigen 19-9 (CA199) were examined. Resting electrocardiogram (ECG) of 5-min was collected prior to surgical treatments to enable the HRV analysis. Twelve nonlinear HRV indices covering the irregularity, complexity, asymmetry, and temporal correlation of heartbeat fluctuations were obtained. Increased short-range temporal correlations, decreased asymmetry, and increased irregularity of heartbeat fluctuations were associated with higher FIB level. Increased irregularity and decreased complexity were also associated with higher CEA level. These associations were independent of age, sex, BMI, alcohol consumption, history of diabetes, left ventricular ejection fraction, and anemia. The results support the hypothesis that perturbations in nonlinear dynamical patterns of HRV predict increased GC severity. Replication in larger samples as well as the examination of longitudinal associations of HRV nonlinear features with cancer prognosis/survival are warranted. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761171/ /pubmed/31554856 http://dx.doi.org/10.1038/s41598-019-50358-y Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shi, Bo Wang, Lili Yan, Chang Chen, Deli Liu, Mulin Li, Peng Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title | Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title_full | Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title_fullStr | Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title_full_unstemmed | Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title_short | Nonlinear heart rate variability biomarkers for gastric cancer severity: A pilot study |
title_sort | nonlinear heart rate variability biomarkers for gastric cancer severity: a pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761171/ https://www.ncbi.nlm.nih.gov/pubmed/31554856 http://dx.doi.org/10.1038/s41598-019-50358-y |
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