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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Physiol.</journal-id>
<journal-title>Frontiers in Physiology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Physiol.</abbrev-journal-title>
<issn pub-type="epub">1664-042X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fphys.2021.678428</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Physiology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Association of Short-Term Heart Rate Variability With Breast Tumor Stage</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Wu</surname>
<given-names>Shuang</given-names>
</name>
<xref rid="aff1" ref-type="aff"><sup>1</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1254257/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chen</surname>
<given-names>Man</given-names>
</name>
<xref rid="aff1" ref-type="aff"><sup>1</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1457244/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Jingfeng</given-names>
</name>
<xref rid="aff2" ref-type="aff"><sup>2</sup></xref>
<xref rid="aff3" ref-type="aff"><sup>3</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1306764/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Shi</surname>
<given-names>Bo</given-names>
</name>
<xref rid="aff2" ref-type="aff"><sup>2</sup></xref>
<xref rid="aff3" ref-type="aff"><sup>3</sup></xref>
<xref rid="c002" ref-type="corresp"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/743684/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Zhou</surname>
<given-names>Yufu</given-names>
</name>
<xref rid="aff1" ref-type="aff"><sup>1</sup></xref>
<xref rid="c001" ref-type="corresp"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1457246/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup>
<institution>Department of Radiation Oncology, First Affiliated Hospital, Bengbu Medical College</institution>, <addr-line>Bengbu</addr-line>, <country>China</country>
</aff>
<aff id="aff2"><sup>2</sup>
<institution>School of Medical Imaging, Bengbu Medical College</institution>, <addr-line>Bengbu</addr-line>, <country>China</country>
</aff>
<aff id="aff3"><sup>3</sup>
<institution>Anhui Key Laboratory of Computational Medicine and Intelligent Health, Bengbu Medical College</institution>, <addr-line>Bengbu</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn id="fn1" fn-type="edited-by">
<p>Edited by: Julian F. Thayer, The Ohio State University, United States</p>
</fn>
<fn id="fn2" fn-type="edited-by">
<p>Reviewed by: Yori Gidron, UMR9193 Laboratoires Sciences Cognitives et Sciences Affectives (SCALab), France; Raquel Bail&#x00F3;n, University of Zaragoza, Spain</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Yufu Zhou, <email>byyfyzyf@163.com</email></corresp>
<corresp id="c002">Bo Shi, <email>shibo@bbmc.edu.cn</email></corresp>
<fn id="fn3" fn-type="other">
<p>This article was submitted to Autonomic Neuroscience, a section of the journal Frontiers in Physiology</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>10</day>
<month>09</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>12</volume>
<elocation-id>678428</elocation-id>
<history>
<date date-type="received">
<day>09</day>
<month>03</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>18</day>
<month>08</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2021 Wu, Chen, Wang, Shi and Zhou.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Wu, Chen, Wang, Shi and Zhou</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Cardiac autonomic modulation, assessed by heart rate variability (HRV), is associated with tumor pathogenesis and development as well as invasion and metastasis. This study aimed to examine this association in breast cancer (BC) patients. A total of 133 patients (average age 49.2years) with BC or benign breast tumors were divided into three groups: benign group, early-stage group, and advanced-stage group. About 5-min resting ECG was collected for the analysis of linear and nonlinear HRV parameters. Multiple logistic regression models were performed to test the independent contribution of HRV to breast tumor stage. The advanced-stage group had significantly reduced HRV compared to the benign and early-stage groups. In particular, for each 1-SD increase in SD2, SD of normal-to-normal intervals, very-low frequency, total power, and low frequency, the odds of having advanced staging decreased by 69.3, 64.3, 58.3, 53.3, and 65.9%, respectively. These associations were independent of age, body mass index, mean heart rate (HR), and respiratory rate (RR). These findings suggest an association between HRV and breast tumor stage, and HRV parameters may help construct an effective early diagnostic and clinical prognostic model.</p>
</abstract>
<kwd-group>
<kwd>autonomic modulation</kwd>
<kwd>breast tumors</kwd>
<kwd>heart rate variability</kwd>
<kwd>nonlinear dynamics</kwd>
<kwd>tumor-node-metastasis stages</kwd>
</kwd-group>
<contract-num rid="cn1">BY51201312</contract-num>
<contract-num rid="cn2">BYKC201905</contract-num>
<contract-num rid="cn3">byycx20103</contract-num>
<contract-sponsor id="cn1">Outstanding Talents Fostering Project of Bengbu Medical College</contract-sponsor>
<contract-sponsor id="cn2">Scientific Research Innovation Project of Bengbu Medical College</contract-sponsor>
<contract-sponsor id="cn3">Students Scientific Research Innovation Project of Bengbu Medical College</contract-sponsor>
<counts>
<fig-count count="1"/>
<table-count count="4"/>
<equation-count count="0"/>
<ref-count count="37"/>
<page-count count="8"/>
<word-count count="6186"/>
</counts>
</article-meta>
</front>
<body>
<sec id="sec1" sec-type="intro">
<title>Introduction</title>
<p>Breast cancer (BC) is the most common cancer among women worldwide. In 2020, approximately 2.26 million new cases of BC were diagnosed. BC represents approximately 11.7% of all cancers and is the fifth leading cause of cancer deaths worldwide (680,000 deaths; <xref ref-type="bibr" rid="ref31">Sung et al., 2021</xref>).</p>
<p>The vagus nerve, a major part of the parasympathetic nerve system, regulates the development and progression of cancer (<xref ref-type="bibr" rid="ref9">De Couck and Gidron, 2013</xref>). Increased vagal nerve activity has a profound inhibitory effect on oxidative stress, DNA cell damage, inflammation, and sympathetic nervous system overreaction (<xref ref-type="bibr" rid="ref19">Maki et al., 2006</xref>; <xref ref-type="bibr" rid="ref33">Tsutsumi et al., 2007</xref>; <xref ref-type="bibr" rid="ref32">Tracey, 2009</xref>; <xref ref-type="bibr" rid="ref11">De Couck et al., 2012</xref>). Studies have demonstrated the bidirectional relationship between cancer and decreased vagal nerve activity (<xref ref-type="bibr" rid="ref8">De Couck et al., 2018</xref>). Therefore, study of the vagus nerve could provide valuable prognostic information and guide therapy in breast cancer.</p>
<p>Heart rate variability (HRV) is a promising biomarker that can be used to evaluate autonomic nervous system function and it may be associated with vagal nerve function (<xref ref-type="bibr" rid="ref34">Vanderlei et al., 2009</xref>; <xref ref-type="bibr" rid="ref16">Karvinen et al., 2013</xref>). One group showed the clinical significance of HRV in patients with BC (<xref ref-type="bibr" rid="ref1">Arab et al., 2016</xref>). However, few studies have explored the association of HRV with tumor-node-metastasis (TNM) in patients with BC.</p>
<p>In a previous study, patients with BC had lower the SD of all normal-to-normal intervals (SDNN) and the root mean square of successive interval differences (RMSSD) than women without BC, no matter how long after the surgery (<xref ref-type="bibr" rid="ref27">Palma et al., 2016</xref>). In addition, <xref ref-type="bibr" rid="ref2">Arab et al. (2018)</xref> found that SDNN and RMSSD negatively correlated with BC staging after analyzing time and frequency domains of HRV in patients. In patients with advanced-stage BC, low SDNN might be correlated with a poor prognosis. <xref ref-type="bibr" rid="ref17">Kim et al. (2010)</xref> reported that an SDNN value of &#x003C;21.3ms in brain metastasis predicted poor survival, while <xref ref-type="bibr" rid="ref37">Wang et al. (2013)</xref> found that an SDNN value of &#x003C;10ms in terminal-stage cancer predicted poor survival. These studies suggested a potential role of time-domain parameters of HRV as a prognostic factor. However, further research is warranted to clarify the potential role of time-domain parameters in the survival of patients with advanced-stage BC.</p>
<p>Previous studies indicated that higher resting high-frequency power (HF) was strongly associated with longer overall survival in patients with recurrent or metastatic BC (<xref ref-type="bibr" rid="ref13">Giese-Davis et al., 2015</xref>). <xref ref-type="bibr" rid="ref7">Chiang et al. (2010)</xref> found that the survival time of patients with terminal hepatocellular carcinoma was significantly related to HF. These studies suggested that, as a long-term predictor of survivors, HF may offer early estimation of clinical prognosis for cancer patients. More importantly, the results of these studies also indicated that HF strongly positively correlated with prognosis, particularly in patients with advanced-stage cancer. The vagal nerve activity might be of more importance in advanced stages.</p>
<p>Therefore, this study aimed to compare short-term HRV in the tumor stage of patients with BC. It was hypothesized that HRV in patients with advanced cancer would be lower than that in patients with early-stage disease. The analysis confirmed the aforementioned hypothesis and had clinical implications: HRV might be a potentially feasible tool in clinic to evaluate the prognosis of BC. More importantly, clinicians could ascertain patients at risk for disease progression through the long-term monitoring of HRV.</p>
</sec>
<sec id="sec2" sec-type="materials|methods">
<title>Materials and Methods</title>
<sec id="sec3">
<title>Participants and Procedures</title>
<p>This study followed the regulations of the National Research Ethics Committee and obtained the approval of the Clinical Medical Research Ethics Committee of the First Affiliated Hospital of Bengbu Medical College (Bengbu, Anhui, China; registration number: 2019KY031). In this study, women diagnosed with breast tumors were selected by the pathological examination from 2019 to 2020. All participants volunteered for this study and provided informed consent.</p>
<p>The function of the vagal nervous system was assessed by analyzing HRV using an ECG recorder (HeaLink-R211B; HeaLink Ltd., Bengbu, China). The sampling rate of the ECG signal was 400Hz. ECG data were collected at room temperature (23&#x00B1;1&#x00B0;C) and always 3days prior to radiotherapy/operation. Participants were explained the ECG collection procedure and were asked to assume the supine position and keep quiet during ECG examination. The ECG acquisition time using V5-lead was 5min.</p>
<p>The following conditions that are known to alter HRV were used as exclusion criteria: (1) diabetes mellitus; (2) heart diseases; (3) use of anti-arrhythmic drugs or beta-blockers; (4) pacemaker; (5) poor ECG quality; (6) ectopic beats (&#x003E;10% of all beats); and (7) chemotherapy or surgery in the 3weeks before the examination. Therefore, our study analyzed the data of 133 participants.</p>
</sec>
<sec id="sec4">
<title>HRV Analysis</title>
<p>The ECG R peaks were extracted using an algorithm based on the Pan&#x2013;Tompkins algorithm (<xref ref-type="bibr" rid="ref28">Pan and Tompkins, 1985</xref>). The technical and physiological artifacts within R-R intervals (RRI) were corrected by applying an automatic artefact correction algorithm. Subsequent HRV indices for both linear (time and frequency domain) and nonlinear methods were calculated.</p>
<p>Commonly used time-domain indices include SDNN and RMSSD. SDNN, a total variability index, represents the involvement of all cyclic components. RMSSD reflects parasympathetic activity (<xref ref-type="bibr" rid="ref6">Camm et al., 1996</xref>; <xref ref-type="bibr" rid="ref34">Vanderlei et al., 2009</xref>).</p>
<p>The RRI time series was converted into power spectral analysis to analyze the frequency domain, and the power spectral density was obtained using the Fast Fourier Transform algorithm. Prior to frequency-domain analysis, the RRI time series was evenly resampled at 4Hz using cubic spline interpolation. Frequency-domain parameters included total power (TP, 0&#x2013;0.4Hz), high-frequency power (HF, 0.15&#x2013;0.4Hz), low-frequency power (LF, 0.04&#x2013;0.15Hz), very-low frequency power (VLF, 0&#x2013;0.04Hz), and the ratio of LF to HF (LF/HF). LF and HF parameters were expressed in normalized units: normalized HF [HF n.u. =HF/(TP &#x2013; VLF)] and normalized LF [LF n.u. =LF/(TP &#x2013; VLF); <xref ref-type="bibr" rid="ref22">Montano et al., 1994</xref>; <xref ref-type="bibr" rid="ref6">Camm et al., 1996</xref>; <xref ref-type="bibr" rid="ref34">Vanderlei et al., 2009</xref>].</p>
<p>The LF corresponds to the co-regulation of sympathetic and vagal nerve tones, HF indicates the vagal nerve tone, and the LF/HF reflects interactions of both sympathetic nervous system and parasympathetic nervous system, but they are limited to the case where the respiratory frequency is in the HF band (<xref ref-type="bibr" rid="ref15">Hernando et al., 2016</xref>; <xref ref-type="bibr" rid="ref35">Varon et al., 2019</xref>). The difference in respiratory rate (RR) will lead to the analysis of HRV in the standard frequency band cannot accurately estimate the activity of autonomic nervous system. For example, when the RR is higher than the upper limit of the HF band, vagus activity may be underestimated. In contrast, when the RR is within the LF band, sympathetic activity is overestimated and vagus activity is underestimated. Therefore, respiratory influences need to be separated in order to better estimate the activity of sympathetic and vagus nerves (<xref ref-type="bibr" rid="ref35">Varon et al., 2019</xref>). An estimate of RR was calculated using an ECG-derived respiration approach (<xref ref-type="bibr" rid="ref23">Moody et al., 1985</xref>). It is important to check whether RR is below 0.15Hz or higher than 0.4Hz in all the enrolled subjects, in order to trust in the interpretation of LF and HF related indices.</p>
<p>Each RRI time series included eight nonlinear HRV indices, including approximate entropy (ApEn), sample entropy (SampEn), Poincare plot: SD1, SD2, and SD2/SD1, detrended fluctuation analysis (DFA): &#x03B1;1 and &#x03B1;2, and correlation dimension (CD). The estimated ApEn and SampEn depended on three parameters: the embedding dimension <italic>m</italic>, the tolerance value <italic>r</italic>, and the data length <italic>N</italic>. The parameters are set as <italic>m</italic>=2 and <italic>r</italic>=0.2<italic>&#x03C3;</italic>, where <italic>&#x03C3;</italic> was the SD of each realization (<xref ref-type="bibr" rid="ref6">Camm et al., 1996</xref>; <xref ref-type="bibr" rid="ref34">Vanderlei et al., 2009</xref>; <xref ref-type="bibr" rid="ref36">Voss et al., 2009</xref>; <xref ref-type="bibr" rid="ref12">de Godoy, 2016</xref>).</p>
<p>All the above processing steps were performed using the Kubios HRV Premium software (version 3.1.0, Kubios Oy, Kuopio, Finland).<xref rid="fn0001" ref-type="fn"><sup>1</sup></xref></p>
</sec>
<sec id="sec5">
<title>Breast Tumor Groups</title>
<p>Patients with breast tumors were divided into three groups: benign group, early-stage group, and advanced-stage group. Patients with benign breast tumors (i.e., benign epithelial proliferations, intraductal papilloma, phyllodes tumor, breast hyperplasia, and fibroadenomas) were selected as the controls. According to the National Comprehensive Cancer Network Clinical Practice Guidelines TNM staging version 3.2020 (<xref ref-type="bibr" rid="ref14">Gradishar et al., 2020</xref>), the remaining participants were divided into early-stage and advanced-stage groups. The early-stage group consisted of T1&#x2013;2, N0&#x2013;1, and M0, and T3N0M0 cancers, while the advanced-stage group consisted of T0&#x2013;4, any N, and M0&#x2013;1 cancers. The non-advanced-stage group included controls and early-stage patients.</p>
</sec>
<sec id="sec6">
<title>Statistical Analysis</title>
<p>Descriptive statistical data were expressed as mean (SD), median (Q1, Q3), or percentage. The Shapiro&#x2013;Wilk test was used to test the normality of HRV indices. A chi-square test was used to analyze the difference between the two cancer groups. Dependent variable analyses for linear and nonlinear HRV parameters were separately conducted using parametric and nonparametric tests. One-way ANOVA was used to calculate normal data and Fisher&#x2019;s least significant difference (LSD) was used for multiple comparisons between groups. The Kruskal&#x2013;Wallis test was used to analyze non-normal data. Finally, separate multiple logistic regression models were performed with breast tumor stage as an outcome and with each significant HRV parameter set as a predictor while adjusted for age, body mass index (BMI), mean heart rate (HR), and RR. SPSS Statistics 25.0 (IBM Corp., Chicago, Illinois, United States) was used, and a value of <italic>p</italic>&#x003C;0.05 was considered statistically significant.</p>
</sec>
</sec>
<sec id="sec7" sec-type="results">
<title>Results</title>
<p><xref rid="tab1" ref-type="table">Table 1</xref> presents the demographics and HRV indices of patients with breast tumors. In TNM staging, the early-stage group mainly comprised patients with stages T1&#x2013;2, N0&#x2013;1, and M0 cancers, while the advanced-stage group commonly comprised patients with stages T1&#x2013;3, N2&#x2013;3, and M0 cancers. Twelve patients in the advanced-stage group had distant metastases to the brain, bones, and lungs. Among patients with stages I&#x2013;IV, the early-stage group mostly comprised stages Ia, IIa, and IIb; however, the advanced-stage group mostly comprised stage IIIa, IIIc, and IV. Invasive carcinoma with no special type is mostly frequent in patients with BC. The early-stage group had a more noninvasive type of BC compared to the advanced-stage group. The results of the molecular typing revealed no significant differences between the groups (<xref rid="tab2" ref-type="table">Table 2</xref>).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Demographics and heart rate variability (HRV) of breast tumor patients.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Variables</th>
<th align="left" valign="top">Values</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">
<italic>N</italic> (Female)</td>
<td align="center" valign="middle">133</td>
</tr>
<tr>
<td align="left" valign="middle">Age (years)</td>
<td align="center" valign="middle">49.2 (10.5)</td>
</tr>
<tr>
<td align="left" valign="middle">BMI (kg/m<sup>2</sup>)</td>
<td align="center" valign="middle">24.5 (3.6)</td>
</tr>
<tr>
<td align="left" valign="middle">Mean HR (bpm)</td>
<td align="center" valign="middle">79.8 (11.5)</td>
</tr>
<tr>
<td align="left" valign="middle">RR (Hz)</td>
<td align="center" valign="middle">0.31 (0.05)</td>
</tr>
<tr>
<td align="left" valign="middle">SDNN (ms)</td>
<td align="center" valign="middle">28.8 (11.5)</td>
</tr>
<tr>
<td align="left" valign="middle">RMSSD (ms)</td>
<td align="center" valign="middle">17.1 (10.3, 24.1)</td>
</tr>
<tr>
<td align="left" valign="middle">VLF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">359 (167, 573)</td>
</tr>
<tr>
<td align="left" valign="middle">LF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">116 (59, 260)</td>
</tr>
<tr>
<td align="left" valign="middle">HF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">122 (55, 255)</td>
</tr>
<tr>
<td align="left" valign="middle">TP (ms<sup>2</sup>)</td>
<td align="center" valign="middle">640 (344, 1,072)</td>
</tr>
<tr>
<td align="left" valign="middle">LF n.u. (%)</td>
<td align="center" valign="middle">53.1 (18.7)</td>
</tr>
<tr>
<td align="left" valign="middle">HF n.u. (%)</td>
<td align="center" valign="middle">47.1 (18.7)</td>
</tr>
<tr>
<td align="left" valign="middle">LF/HF</td>
<td align="center" valign="middle">1.102 (0.599, 2.114)</td>
</tr>
<tr>
<td align="left" valign="middle">SD1 (ms)</td>
<td align="center" valign="middle">12.1 (7.3, 16.9)</td>
</tr>
<tr>
<td align="left" valign="middle">SD2 (ms)</td>
<td align="center" valign="middle">38.1 (14.8)</td>
</tr>
<tr>
<td align="left" valign="middle">SD2/SD1</td>
<td align="center" valign="middle">3.392 (1.270)</td>
</tr>
<tr>
<td align="left" valign="middle">ApEn</td>
<td align="center" valign="middle">1.126 (0.091)</td>
</tr>
<tr>
<td align="left" valign="middle">SampEn</td>
<td align="center" valign="middle">1.441 (0.268)</td>
</tr>
<tr>
<td align="left" valign="middle">&#x03B1;<sub>1</sub>
</td>
<td align="center" valign="middle">1.068 (0.263)</td>
</tr>
<tr>
<td align="left" valign="middle">&#x03B1;<sub>2</sub>
</td>
<td align="center" valign="middle">1.070 (0.188)</td>
</tr>
<tr>
<td align="left" valign="middle">CD</td>
<td align="center" valign="middle">0.494 (0.228, 0.974)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>ApEn, approximate entropy; BMI, body mass index; bpm, beats per minute; CD, correlation dimension; RR, respiration rate; HR, heart rate; HF, high-frequency power; LF, low-frequency power; LF/HF, ratio of low-frequency power to high-frequency power; N, number of individuals; RMSSD, root mean square of successive interval differences; SampEn, sample entropy; SD, standard deviation; SDNN, SD of all normal-to-normal intervals; TP, total power; and VLF, very low frequency. Values are expressed as the number of patients, mean (SD), or median (Q1, Q3).</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Clinical characteristics of breast cancer (BC) patients.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="left" valign="top">Early stage (<italic>N</italic>=50) (%)</th>
<th align="left" valign="top">Advanced stage (<italic>N</italic>=40) (%)</th>
<th align="left" valign="top">
<italic>p</italic>
</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" colspan="4">TNM staging</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">T &#x2013; primary tumor in greatest dimension</td>
</tr>
<tr>
<td align="left" valign="top">T1 (&#x2264;20mm)</td>
<td align="center" valign="top">20 (40)</td>
<td align="center" valign="top">11 (27.5)</td>
<td align="center" valign="top" rowspan="4">
<bold>0.002</bold>
</td>
</tr>
<tr>
<td align="left" valign="top">T2 (&#x003E;20mm and&#x2264;50)</td>
<td align="center" valign="top">28 (56)</td>
<td align="center" valign="top">15 (37.5)</td>
</tr>
<tr>
<td align="left" valign="top">T3 (&#x003E;50mm)</td>
<td align="center" valign="top">2 (4)</td>
<td align="center" valign="top">9 (22.5)</td>
</tr>
<tr>
<td align="left" valign="top">T4 (any size with extension to the chest wall and/or to the skin &#x2013; ulceration or skin nodules)</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">5 (12.5)</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">N &#x2013; regional lymph nodes metastases</td>
</tr>
<tr>
<td align="left" valign="top">N0 (none)</td>
<td align="center" valign="top">35 (70)</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top" rowspan="4">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="top">N1</td>
<td align="center" valign="top">15 (30)</td>
<td align="center" valign="top">5 (12.5)</td>
</tr>
<tr>
<td align="left" valign="top">N2</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">16 (40)</td>
</tr>
<tr>
<td align="left" valign="top">N3</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">19 (47.5)</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">M &#x2013; distant metastases</td>
</tr>
<tr>
<td align="left" valign="top">M0 (no clinical or radiographic evidence)</td>
<td align="center" valign="top">50 (100)</td>
<td align="center" valign="top">28 (70)</td>
<td align="center" valign="top" rowspan="2">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="top">M1 (with distant detectable metastases)</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">12 (30)</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">I&#x2013;IV staging</td>
</tr>
<tr>
<td align="left" valign="top">Ia &#x2013; T1, N0, M0</td>
<td align="center" valign="top">16 (32)</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top" rowspan="8">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="top">Ib &#x2013; T0&#x2013;1, N1 micrometastases, M0</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">0 (0)</td>
</tr>
<tr>
<td align="left" valign="top">IIa &#x2013; T0&#x2013;1, N1, M0 or T2, N0, M0</td>
<td align="center" valign="top">21 (42)</td>
<td align="center" valign="top">0 (0)</td>
</tr>
<tr>
<td align="left" valign="top">IIb &#x2013; T2, N1, M0 or T3, N0, M0</td>
<td align="center" valign="top">13 (26)</td>
<td align="center" valign="top">0 (0)</td>
</tr>
<tr>
<td align="left" valign="top">IIIa &#x2013; T0&#x2013;2, N2, M0 or T3, N1&#x2013;2, M0</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">13 (32.5)</td>
</tr>
<tr>
<td align="left" valign="top">IIIb &#x2013; T4, N0&#x2013;2, M0</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">3 (7.5)</td>
</tr>
<tr>
<td align="left" valign="top">IIIc &#x2013; T0&#x2013;4, N3, M0</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">12 (30)</td>
</tr>
<tr>
<td align="left" valign="top">IV &#x2013; T0&#x2013;4, N0&#x2013;3, M1</td>
<td align="center" valign="top">0 (0)</td>
<td align="center" valign="top">12 (30)</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Type of breast cancer</td>
</tr>
<tr>
<td align="left" valign="top">Noninvasive type</td>
<td align="center" valign="top">11 (22)</td>
<td align="center" valign="top">3 (7.5)</td>
<td align="center" valign="top" rowspan="3">0.169</td>
</tr>
<tr>
<td align="left" valign="top">Invasive (no special type)</td>
<td align="center" valign="top">38 (76)</td>
<td align="center" valign="top">36 (90)</td>
</tr>
<tr>
<td align="left" valign="top">Invasive (special type)</td>
<td align="center" valign="top">1 (2)</td>
<td align="center" valign="top">1 (2.5)</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Molecular typing</td>
</tr>
<tr>
<td align="left" valign="top">Luminal A</td>
<td align="center" valign="top">12 (24)</td>
<td align="center" valign="top">10 (25)</td>
<td align="center" valign="top" rowspan="4">0.794</td>
</tr>
<tr>
<td align="left" valign="top">Luminal B</td>
<td align="center" valign="top">19 (38)</td>
<td align="center" valign="top">14 (35)</td>
</tr>
<tr>
<td align="left" valign="top">Her-2 overexpressing</td>
<td align="center" valign="top">10 (20)</td>
<td align="center" valign="top">11 (27.5)</td>
</tr>
<tr>
<td align="left" valign="top">Triple negative</td>
<td align="center" valign="top">9 (18)</td>
<td align="center" valign="top">5 (12.5)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Values are expressed as the number of individuals (percentages). Bold values of <italic>p</italic> indicate statistical significance (<italic>p</italic>&#x003C;0.05). Luminal A: ER/PR (+), HER2 (&#x2212;), and ki-67 &#x003C;14%. Luminal B: ER/PR (+), HER2 (&#x2212;), and ki-67 &#x2265;14%; ER/PR/HER2 (+), any level of ki-67. Her-2-overexpressing: ER/PR (&#x2212;) and HER2 (+). Triple negative: ER/PR/HER2 (&#x2212;).</p>
</table-wrap-foot>
</table-wrap>
<p>Differences in SDNN (<italic>p</italic>&#x003C;0.001), RMSSD (<italic>p</italic>=0.006), VLF (<italic>p</italic>&#x003C;0.001), LF (<italic>p</italic>&#x003C;0.001), HF (<italic>p</italic>=0.005), TP (<italic>p</italic>&#x003C;0.001), SD1 (<italic>p</italic>=0.007), SD2 (<italic>p</italic>&#x003C;0.001), and CD (<italic>p</italic>&#x003C;0.001) between groups were shown using one-way ANOVA and Kruskal&#x2013;Wallis test. Furthermore, SDNN, RMSSD, VLF, LF, HF, TP, SD1, SD2, and CD were significantly decreased in the advanced-stage group compared to the corresponding values in the benign and early-stage groups. However, differences in HRV indices between the benign and early-stage groups were not significantly different. Moreover, there were no statistically significant differences in the LF n.u, HF n.u, LF/HF, SD2/SD1, ApEn, SampEn, &#x03B1;<sub>1</sub>, and &#x03B1;<sub>2</sub> among the groups (<xref rid="tab3" ref-type="table">Table 3</xref>).</p>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>Comparison of HRV parameters among the benign, early-stage, and advanced-stage groups.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Variables</th>
<th align="left" valign="top">Benign (<italic>N</italic>=43)</th>
<th align="left" valign="top">Early stage (<italic>N</italic>=50)</th>
<th align="left" valign="top">Advanced stage (<italic>N</italic>=40)</th>
<th align="left" valign="top">
<italic>p</italic>
</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Mean HR (bpm)</td>
<td align="center" valign="middle">78.9&#x00B1;11.7</td>
<td align="center" valign="middle">77.9&#x00B1;10.5</td>
<td align="center" valign="middle">83.0&#x00B1;12.2</td>
<td align="center" valign="middle">0.099</td>
</tr>
<tr>
<td align="left" valign="middle">RR (Hz)</td>
<td align="center" valign="middle">0.30&#x00B1;0.04</td>
<td align="center" valign="middle">0.31&#x00B1;0.05</td>
<td align="center" valign="middle">0.31&#x00B1;0.06</td>
<td align="center" valign="middle">0.489</td>
</tr>
<tr>
<td align="left" valign="middle">SDNN (ms)</td>
<td align="center" valign="middle">32.7&#x00B1;9.3</td>
<td align="center" valign="middle">29.3&#x00B1;11.6</td>
<td align="center" valign="middle">23.1&#x00B1;11.6<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">RMSSD (ms)</td>
<td align="center" valign="middle">19.2 (13.8, 27.4)</td>
<td align="center" valign="middle">18.6 (12.2, 27.8)</td>
<td align="center" valign="middle">11.2 (8.0, 18.0)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>0.006</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">VLF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">443 (259, 674)</td>
<td align="center" valign="middle">410 (177, 604)</td>
<td align="center" valign="middle">199 (103, 355)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">LF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">155 (102, 297)</td>
<td align="center" valign="middle">154 (59, 295)</td>
<td align="center" valign="middle">66 (37, 142)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">HF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">151 (78, 300)</td>
<td align="center" valign="middle">151 (55, 270)</td>
<td align="center" valign="middle">60 (23, 136)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>0.005</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">TP (ms<sup>2</sup>)</td>
<td align="center" valign="middle">903 (485, 1,147)</td>
<td align="center" valign="middle">781 (429, 1,190)</td>
<td align="center" valign="middle">351 (187, 619)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">LF n.u. (%)</td>
<td align="center" valign="middle">52.7&#x00B1;18.6</td>
<td align="center" valign="middle">54.4&#x00B1;18.9</td>
<td align="center" valign="middle">52.0&#x00B1;18.9</td>
<td align="center" valign="middle">0.821</td>
</tr>
<tr>
<td align="left" valign="middle">HF n.u. (%)</td>
<td align="center" valign="middle">47.2&#x00B1;18.5</td>
<td align="center" valign="middle">46.4&#x00B1;19.1</td>
<td align="center" valign="middle">48.0&#x00B1;18.9</td>
<td align="center" valign="middle">0.927</td>
</tr>
<tr>
<td align="left" valign="middle">LF/HF</td>
<td align="center" valign="middle">1.214 (0.682, 2.030)</td>
<td align="center" valign="middle">1.401 (0.579, 2.213)</td>
<td align="center" valign="middle">0.952 (0.597, 2.165)</td>
<td align="center" valign="middle">0.852</td>
</tr>
<tr>
<td align="left" valign="middle">SD1 (ms)</td>
<td align="center" valign="middle">13.6 (9.8, 17.3)</td>
<td align="center" valign="middle">13.1 (8.7, 19.7)</td>
<td align="center" valign="middle">8.0 (5.7, 12.8)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>0.007</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">SD2 (ms)</td>
<td align="center" valign="middle">43.8&#x00B1;12.7</td>
<td align="center" valign="middle">39.6&#x00B1;14.8</td>
<td align="center" valign="middle">30.2&#x00B1;13.8<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">SD2/SD1</td>
<td align="center" valign="middle">3.444&#x00B1;1.237</td>
<td align="center" valign="middle">3.348&#x00B1;1.358</td>
<td align="center" valign="middle">3.391&#x00B1;1.220</td>
<td align="center" valign="middle">0.937</td>
</tr>
<tr>
<td align="left" valign="middle">ApEn</td>
<td align="center" valign="middle">1.10&#x00B1;0.10</td>
<td align="center" valign="middle">1.13&#x00B1;0.10</td>
<td align="center" valign="middle">1.15&#x00B1;0.10</td>
<td align="center" valign="middle">0.055</td>
</tr>
<tr>
<td align="left" valign="middle">SampEn</td>
<td align="center" valign="middle">1.40&#x00B1;0.27</td>
<td align="center" valign="middle">1.47&#x00B1;0.27</td>
<td align="center" valign="middle">1.46&#x00B1;0.26</td>
<td align="center" valign="middle">0.411</td>
</tr>
<tr>
<td align="left" valign="middle">&#x03B1;<sub>1</sub>
</td>
<td align="center" valign="middle">1.11&#x00B1;0.26</td>
<td align="center" valign="middle">1.07&#x00B1;0.27</td>
<td align="center" valign="middle">1.02&#x00B1;0.25</td>
<td align="center" valign="middle">0.355</td>
</tr>
<tr>
<td align="left" valign="middle">&#x03B1;<sub>2</sub>
</td>
<td align="center" valign="middle">1.05&#x00B1;0.19</td>
<td align="center" valign="middle">1.07&#x00B1;0.18</td>
<td align="center" valign="middle">1.09&#x00B1;0.19</td>
<td align="center" valign="middle">0.557</td>
</tr>
<tr>
<td align="left" valign="middle">CD</td>
<td align="center" valign="middle">0.73 (0.39, 1.05)</td>
<td align="center" valign="middle">0.56 (0.31, 1.69)</td>
<td align="center" valign="middle">0.20 (0.08, 0.57)<xref rid="tfn1" ref-type="table-fn"><sup>&#x002A;</sup></xref><sup>,</sup>
<xref rid="tfn2" ref-type="table-fn"><sup>&#x2020;</sup></xref>
</td>
<td align="center" valign="middle">
<bold>&#x003C;0.001</bold>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>ApEn, approximate entropy; bpm, beats per minute; CD, correlation dimension; HF, high-frequency power; HR, heart rate; LF, low-frequency power; LF/HF, ratio of low-frequency power to high-frequency power; RMSSD, root mean square of successive interval differences; RR, respiration rate; SampEn, sample entropy; SD, standard deviation; SDNN, standard deviation of all normal-to-normal intervals; TP, total power; and VLF, very low frequency. Values are expressed as mean (SD) with normal distribution or median (Q1, Q3) without normal distribution. Bold values of p indicate statistical significance (value of <italic>p</italic>&#x003C;0.05).</p>
<fn id="tfn1">
<label>&#x002A;</label>
<p>
<italic>p</italic>&#x003C;0.05 advanced-stage group vs. benign group.</p>
</fn>
<fn id="tfn2">
<label>&#x2020;</label>
<p>
<italic>p</italic>&#x003C;0.05 advanced-stage group vs. early-stage group.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>With SDNN=20ms as the cutoff value, the subjects were divided into two subgroups: a low-SDNN subgroup (SDNN&#x003C;20ms; <italic>n</italic>=31) and a high-SDNN subgroup (SDNN&#x003E;20ms; <italic>n</italic>=102). There was no statistically significant difference in age between the non-advanced and advanced groups (low-SDNN subgroup, <italic>p</italic>=0.311; high-SDNN subgroup, <italic>p</italic>=0.218; <xref rid="fig1" ref-type="fig">Figure 1</xref>).</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Subgroup analysis of age between non-advanced and advanced groups.</p>
</caption>
<graphic xlink:href="fphys-12-678428-g001.tif"/>
</fig>
<p>To test the independent contribution of HRV to breast tumor stage, we performed multiple logistic regression models after adjusting for age, BMI, mean HR, and RR (<xref rid="tab4" ref-type="table">Table 4</xref>). The associations of tumor stage with SD2, SDNN, VLF, TP, and LF were significant in logistic regression analysis. Specifically, for each 1-SD increase in SD2, SDNN, VLF, TP, and LF, the odds of having advanced staging decreased by 69.3% [odds ratio (OR): 0.307, 95% CI: (0.155, 0.606)], 64.3% [OR: 0.357, 95% CI: (0.183, 0.694)], 58.3% [OR: 0.417, 95% CI: (0.216, 0.807)], 53.3% [OR: 0.467, 95% CI: (0.239, 0.910)], and 65.9% [OR: 0.341, 95% CI: (0.130, 0.898)], respectively. The associations of tumor stage with CD, RMSSD, SD1, and HF were not significant in the logistic regression models.</p>
<table-wrap position="float" id="tab4">
<label>Table 4</label>
<caption>
<p>Results from Logistic regression models (adjusted for age, BMI, Mean HR, and RR).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top" rowspan="2">Variables</th>
<th align="left" valign="top" rowspan="2">OR</th>
<th align="left" valign="top" colspan="2">95% CI for OR</th>
<th align="left" valign="top" rowspan="2">
<italic>p</italic>
</th>
</tr>
<tr>
<th align="left" valign="top">Lower</th>
<th align="left" valign="top">Upper</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">SD2 (ms)</td>
<td align="center" valign="middle">0.307</td>
<td align="center" valign="middle">0.155</td>
<td align="center" valign="middle">0.606</td>
<td align="center" valign="middle">
<bold>0.001</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">SDNN (ms)</td>
<td align="center" valign="middle">0.357</td>
<td align="center" valign="middle">0.183</td>
<td align="center" valign="middle">0.694</td>
<td align="center" valign="middle">
<bold>0.002</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">VLF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">0.417</td>
<td align="center" valign="middle">0.216</td>
<td align="center" valign="middle">0.807</td>
<td align="center" valign="middle">
<bold>0.009</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">TP (ms<sup>2</sup>)</td>
<td align="center" valign="middle">0.467</td>
<td align="center" valign="middle">0.239</td>
<td align="center" valign="middle">0.910</td>
<td align="center" valign="middle">
<bold>0.025</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">LF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">0.341</td>
<td align="center" valign="middle">0.130</td>
<td align="center" valign="middle">0.898</td>
<td align="center" valign="middle">
<bold>0.029</bold>
</td>
</tr>
<tr>
<td align="left" valign="middle">CD</td>
<td align="center" valign="middle">0.599</td>
<td align="center" valign="middle">0.326</td>
<td align="center" valign="middle">1.099</td>
<td align="center" valign="middle">0.098</td>
</tr>
<tr>
<td align="left" valign="middle">RMSSD (ms)</td>
<td align="center" valign="middle">0.848</td>
<td align="center" valign="middle">0.492</td>
<td align="center" valign="middle">1.462</td>
<td align="center" valign="middle">0.553</td>
</tr>
<tr>
<td align="left" valign="middle">SD1 (ms)</td>
<td align="center" valign="middle">0.869</td>
<td align="center" valign="middle">0.505</td>
<td align="center" valign="middle">1.495</td>
<td align="center" valign="middle">0.612</td>
</tr>
<tr>
<td align="left" valign="middle">HF (ms<sup>2</sup>)</td>
<td align="center" valign="middle">1.000</td>
<td align="center" valign="middle">0.632</td>
<td align="center" valign="middle">1.583</td>
<td align="center" valign="middle">1.000</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>BMI, body mass index; CI, confidence interval; CD, correlation dimension; HF, high-frequency power; HR, heart rate; LF, low-frequency power; OR, odds ratio; RMSSD, root mean square of successive interval differences; RR, respiration rate; SD, standard deviation; SDNN, standard deviation of all normal-to-normal intervals; TP, total power; and VLF, very low frequency. Bold values of <italic>p</italic> indicate statistical significance (value of <italic>p</italic>&#x003C;0.05).</p>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="sec8" sec-type="discussions">
<title>Discussion</title>
<p>This study aimed to compare the HRV of patients with breast tumors (benign tumors, early-stage BC, and advanced-stage BC) and evaluate the feasibility of HRV as a tool for the early diagnosis and prognosis of BC patients. Our results revealed that patients with advanced-stage BC had lower HRV than those with benign tumors and early-stage BC. However, no statistically significant difference was observed in the HRV indices between the benign and early-stage groups. After adjusting for age, BMI, Mean HR, and RR, our results showed that SD2, SDNN, VLF, TP, and LF were associated with tumor stage.</p>
<p>The vagus nerve also called the wandering nerve, works <italic>via</italic> many neurotransmitters and plays an important role in multiple systems, such as cardiovascular, neuroendocrine, and immunological (<xref ref-type="bibr" rid="ref32">Tracey, 2009</xref>). Studies have showed that the vagal nerve system transmits a variety of signals to the brain in order to restore the body to a steady state (<xref ref-type="bibr" rid="ref32">Tracey, 2009</xref>; <xref ref-type="bibr" rid="ref26">Ohira et al., 2013</xref>). Moreover, published preliminary studies have also demonstrated that vagal nerve tone is vital in the prognosis of cancer. A higher vagal nerve tone may protect cancer patients by reducing inflammation (<xref ref-type="bibr" rid="ref10">De Couck et al., 2016</xref>). Measuring the HRV is a noninvasive approach of measuring vagal nerve activity (<xref ref-type="bibr" rid="ref34">Vanderlei et al., 2009</xref>). HRV is known to be associated with vagal nerve tone (<italic>r</italic>=0.88; <xref ref-type="bibr" rid="ref18">Kuo et al., 2005</xref>). In recent years, various linear and nonlinear methods have been applied to analyze the time series of heartbeat cardiac intervals, reflecting the physiological and pathological information contained in the HRV signal from different angles.</p>
<p>Few studies have explored the association of HRV with TNM in patients with breast cancer. In one study, <xref ref-type="bibr" rid="ref24">Mouton et al. (2012)</xref> examined the data of 72 patients with colorectal cancer and found that the baseline HRV could predict the carcinoembryonic antigen levels at 12months. Moreover, they found that SDNN&#x003C;20ms was associated with significantly higher CEA at 12months. <xref ref-type="bibr" rid="ref1">Arab et al. (2016)</xref> showed the clinical significance of HRV in patients with breast cancer.</p>
<p>Several studies indicated that higher resting HF was strongly associated with longer overall survival in patients with recurrent or metastatic BC (<xref ref-type="bibr" rid="ref13">Giese-Davis et al., 2015</xref>). <xref ref-type="bibr" rid="ref7">Chiang et al. (2010)</xref> found that the survival time of patients with terminal hepatocellular carcinoma was significantly related to HF. More importantly, the results of these studies also indicated that HF strongly positively correlated with prognosis, particularly in patients with advanced-stage cancer. However, despite the interesting results of our study, we did not find any statistically significant differences in the HF among the three cancer stage groups. The difference in mean HR and RR may cause HF to not accurately estimate the cardiac autonomic regulation activity. In our study, the difference was not statistically significant in mean HR and RR between the groups, and the RR of all the enrolled subjects were in the HF band. Therefore, the interpretation of spectral HRV indices as autonomic cardiac regulation markers in our study was more accurate and reliable. The findings of the present study could be verified through a prospective study performed over a longer follow-up period.</p>
<p>Similar to the above results, the median HF at baseline was 122 (IQR, 55, 255) ms<sup>2</sup> in our study, and the median HF values in benign, early-stage, and advanced-stage BC were 151 (78, 300), 151 (55, 270), and 60 (23, 136), respectively, indicating that a higher HF may be associated with benign or early-stage BC, and consequently a better survival rate. However, unlike <xref ref-type="bibr" rid="ref24">Mouton et al. (2012)</xref>, we used a cutoff of SDNN=20ms, and found that the SDNN showed a significant inverse association with tumor stage. A lower SDNN was found to be associated with more advanced-stage BC.</p>
<p>The interpretation of LF/HF is controversial. <xref ref-type="bibr" rid="ref21">Malliani et al. (1991)</xref> showed that the LF/HF could reflect the balance between the vagus nerve and the sympathetic nerve. But LF/HF has been largely criticized as a marker of sympatho-vagal balance (<xref ref-type="bibr" rid="ref4">Billman, 2011</xref>, <xref ref-type="bibr" rid="ref5">2013</xref>). First, LF power is not a pure index of sympathetic nerve, it may also be affected by vagus nerve and other unspecified factors. Second, sympathetic and vagus nerve can be simultaneously active, and their interaction is complex and nonlinear. Third, respiratory parameters and mechanical factors will also cause uncertainty in the contribution of sympathetic and vagus nerve to LF/HF. Finally, HR can affect LF/HF independently of cardiac autonomic nerve activity (<xref ref-type="bibr" rid="ref5">Billman, 2013</xref>). In our study, no statistically significant difference was observed in LF/HF among the three cancer stage groups. This could be because of the complex physiological basis of LF/HF and the other unidentified factors.</p>
<p>Linear methods cannot be used to describe properly the complex nonlinear behavior, which is predominant in human systems. Therefore, it is necessary to search the novel indexes to reflect the correlation and the complexity characteristics of the HRV signal. The characteristic of HRV nonlinear analysis can better express the irregularity, complexity, and other dynamic characteristics of heartbeat fluctuations. Across various studies in the field of cardiovascular disorders, nonlinear dynamical HRV analysis is significantly superior to linear time-domain and frequency-domain methods (<xref ref-type="bibr" rid="ref20">M&#x00E4;kikallio et al., 2001</xref>; <xref ref-type="bibr" rid="ref30">Stein et al., 2005</xref>; <xref ref-type="bibr" rid="ref36">Voss et al., 2009</xref>; <xref ref-type="bibr" rid="ref12">de Godoy, 2016</xref>). Some preliminary studies also explored the correlation between cancer and several nonlinear heartbeat dynamics measurements. <xref ref-type="bibr" rid="ref3">Bettermann et al. (2001)</xref> showed that the variability, complexity, or rhythmicity of HRV in patients with BC was lower than that in patients with diabetes and age-matched healthy women. In particular, while comparing patients with and without BC metastasis, patients with metastasis had lower ApEn compared with those without metastasis. <xref ref-type="bibr" rid="ref29">Shi et al. (2019)</xref> explored the perturbations of HRV nonlinear dynamical patterns to predict the increase in the severity of gastric cancer and found that nonlinear HRV parameters were the markers of autonomic nervous function to tumor progression.</p>
<p>Although, analysis of HRV by methods based on nonlinear dynamics do not reflect vagal or sympathetic regulation, we found significant correlations between time- and frequency domain indices and some of the nonlinear HRV parameters in patients with BC. For example, SampEn, &#x03B1;<sub>1</sub>, and CD correlated with RMSSD [SampEn (<italic>r</italic>=0.546, <italic>p</italic>&#x003C;0.001), &#x03B1;<sub>1</sub> (<italic>r</italic>=&#x2212;0.564, <italic>p</italic>&#x003C;0.001), and CD (<italic>r</italic>=0.800, <italic>p</italic>&#x003C;0.001)], and also correlated with HF [SampEn (<italic>r</italic>=0.521, <italic>p</italic>&#x003C;0.001), &#x03B1;<sub>1</sub> (<italic>r</italic>=&#x2212;0.530, <italic>p</italic>&#x003C;0.001), and CD (<italic>r</italic>=0.792, <italic>p</italic>&#x003C;0.001)]. This illustrates that the nonlinear parameters also contain the component of time-frequency domain index. The nonlinear analysis method is still in the preliminary exploration stage, and the exact physiological and pathological background has not been fully clarified. The findings of the current study might provide new evidence on the role of nonlinear HRV in cancer. Further studies are needed to clarify the correlation of nonlinear HRV as a long-term predictor of survival.</p>
<p>This study had some limitations. First, its cross-sectional study design was a major notable limitation. The correlation between HRV parameters and outcomes could not be inferred. Second, a comprehensive understanding of the connections of nonlinear HRV with BC prognosis is currently lacking. Third, more background variables, such as physical activity, stress levels, use of medications, and other relevant medical variables, could not be included. To address these limitations, studies with larger sample sizes, more detailed background variables, and a prospective design should be conducted to clarify the correlation of linear and nonlinear HRV parameters with BC prognosis.</p>
</sec>
<sec id="sec9" sec-type="conclusions">
<title>Conclusion</title>
<p>This novel study investigated linear and nonlinear HRV parameters in breast tumor groups. It found that the HRV was related to BC staging, indicating a correlation between tumor and HRV. The results of our study showed that patients with advanced-stage BC had lower HRV and might have a poor prognosis, and demonstrated that nonlinear HRV parameters might predict tumor staging in patients with breast tumors. Nonlinear approaches are of great significance in coping well with the nonstationary and nonlinear nature of heartbeat fluctuations. It is suggested that the combined measurement of linear and nonlinear HRV parameters may benefit future investigations. Researchers should identify a comprehensive biomarker for predicting BC prognosis by leveraging existing linear methods and nonlinear indicators. In addition to evaluating tumor stage, vagal nerve activity should be considered to estimate the prognosis of a cancer patient. Vagal nerve activity can be easily assessed and has the potential to provide healthcare professionals with incremental information based on the treatment plans. Future research should investigate the therapeutic potential of vagal nerve activation in cancer treatments through different supportive therapies such as relaxation, exercise interventions, and Traditional Chinese Medicine treatments (<xref ref-type="bibr" rid="ref25">Niederer et al., 2013</xref>).</p>
</sec>
<sec id="sec10" sec-type="data-availability">
<title>Data Availability Statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding authors.</p>
</sec>
<sec id="sec11">
<title>Ethics Statement</title>
<p>This study followed the regulations of the National Research Ethics Committee and obtained the approval of the Clinical Medical Research Ethics Committee of the First Affiliated Hospital of Bengbu Medical College, China. The patients/participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="sec12">
<title>Author Contributions</title>
<p>BS: conceptualization, resource allocation, and review and editing of the manuscript. SW and MC: data collection, interpretation of the results, and manuscript preparation. JW: data analysis. YZ: supervision and resource allocation. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec id="sec13" sec-type="funding-information">
<title>Funding</title>
<p>This study was funded by the &#x201C;512&#x201D; Outstanding Talents Fostering Project of Bengbu Medical College under Grant BY51201312, the Scientific Research Innovation Project of Bengbu Medical College under Grant BYKC201905, and the Students Scientific Research Innovation Project of Bengbu Medical College under Grant byycx20103.</p>
</sec>
<sec id="conf1" sec-type="COI-statement">
<title>Conflict of Interest</title>
<p>A direct family member of BS owns stock in HeaLink Ltd., Bengbu, China.</p>
<p>The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="sec14" sec-type="disclaimer">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
</body>
<back>
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