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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title>Frontiers in Neurology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurol.</abbrev-journal-title>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fneur.2022.791298</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neurology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Brain Network Alterations in Rectal Cancer Survivors With Depression Tendency: Evaluation With Multimodal Magnetic Resonance Imaging</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Zhang</surname> <given-names>Wenwen</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zou</surname> <given-names>Ying</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhao</surname> <given-names>Feng</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Yang</surname> <given-names>Yongqing</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Mao</surname> <given-names>Ning</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Li</surname> <given-names>Yuan</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Huang</surname> <given-names>Gang</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1178009/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Yao</surname> <given-names>Zhijun</given-names></name>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
<xref ref-type="corresp" rid="c003"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1415084/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Hu</surname> <given-names>Bin</given-names></name>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
<xref ref-type="aff" rid="aff8"><sup>8</sup></xref>
<xref ref-type="aff" rid="aff9"><sup>9</sup></xref>
<xref ref-type="aff" rid="aff10"><sup>10</sup></xref>
<xref ref-type="corresp" rid="c004"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/352838/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Department of Radiology, Gansu Provincial Hospital</institution>, <addr-line>Lanzhou</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Information Engineering, Yantai Vocational College</institution>, <addr-line>Yantai</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>School of Computer Science and Technology, Shandong Technology and Business University</institution>, <addr-line>Yantai</addr-line>, <country>China</country></aff>
<aff id="aff4"><sup>4</sup><institution>School of Management Science and Engineering, Shandong Technology and Business University</institution>, <addr-line>Yantai</addr-line>, <country>China</country></aff>
<aff id="aff5"><sup>5</sup><institution>Department of Radiology, Yantai Yuhuangding Hospital</institution>, <addr-line>Yantai</addr-line>, <country>China</country></aff>
<aff id="aff6"><sup>6</sup><institution>Big data and Artificial Intelligence Laboratory, Yantai Yuhuangding Hospital, Qingdao University</institution>, <addr-line>Yantai</addr-line>, <country>China</country></aff>
<aff id="aff7"><sup>7</sup><institution>School of Information Science and Engineering, Lanzhou University</institution>, <addr-line>Lanzhou</addr-line>, <country>China</country></aff>
<aff id="aff8"><sup>8</sup><institution>Gansu Provincial Key Laboratory of Wearable Computing, School of Information Science and Engineering, Lanzhou University</institution>, <addr-line>Lanzhou</addr-line>, <country>China</country></aff>
<aff id="aff9"><sup>9</sup><institution>CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences</institution>, <addr-line>Shanghai</addr-line>, <country>China</country></aff>
<aff id="aff10"><sup>10</sup><institution>Beijing Institute for Brain Disorders, Capital Medical University</institution>, <addr-line>Beijing</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Xuntao Yin, Guangzhou Medical University, China</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Yuanchao Zhang, University of Electronic Science and Technology of China, China; Kai Wu, South China University of Technology, China; Tingshao Zhu, Institute of Psychology (CAS), China</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Yuan Li <email>liy20&#x00040;sdtbu.edu.cn</email></corresp>
<corresp id="c002">Gang Huang <email>keen0999&#x00040;163.com</email></corresp>
<corresp id="c003">Zhijun Yao <email>yaozj&#x00040;lzu.edu.cn</email></corresp>
<corresp id="c004">Bin Hu <email>bh&#x00040;lzu.edu.cn</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Applied Neuroimaging, a section of the journal Frontiers in Neurology</p></fn>
<fn fn-type="equal" id="fn002"><p>&#x02020;These authors have contributed equally to this work and share first authorship</p></fn></author-notes>
<pub-date pub-type="epub">
<day>29</day>
<month>06</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>13</volume>
<elocation-id>791298</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>10</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>05</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2022 Zhang, Zou, Zhao, Yang, Mao, Li, Huang, Yao and Hu.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Zhang, Zou, Zhao, Yang, Mao, Li, Huang, Yao and Hu</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>Surgery and chemotherapy may increase depression tendency in patients with rectal cancer (RC). Nevertheless, few comprehensive studies are conducted on alterations of brain network induced by depression tendency in patients with RC. Resting-state functional magnetic resonance imaging (rs-fMRI) and diffusion tensor imaging (DTI) data were collected from 42 patients with RC with surgery and chemotherapy and 38 healthy controls (HCs). Functional network (FN) was constructed from extracting average time courses in brain regions, and structural network (SN) was established by deterministic tractography. Graph theoretical analysis was used to calculate network properties. Networks resilient of two networks were assessed. Clinical correlation analysis was explored between altered network parameters and Hamilton depression scale (HAMD) score. This study revealed impaired FN and SN at both local and global levels and changed nodal efficiency and abnormal small-worldness property in patients with RC. On the whole, all FNs are more robust than SN. Moreover, compared with HC, patients with RC show less robustness in both networks. Regions with decreased nodal efficiency were associated with HAMD score. These cognitive dysfunctions are mainly attributable to depression-related brain functional and structural network alterations. Brain network reorganization is to prevent patients with RC from more serious depression after surgery and chemotherapy.</p></abstract>
<kwd-group>
<kwd>rectal cancer</kwd>
<kwd>depression tendency</kwd>
<kwd>functional network</kwd>
<kwd>structural network</kwd>
<kwd>multimodal research</kwd>
</kwd-group>
<contract-num rid="cn001">2016YFC1307203</contract-num>
<contract-num rid="cn001">2019YFA0706200</contract-num>
<contract-num rid="cn002">61627808</contract-num>
<contract-num rid="cn002">61632014</contract-num>
<contract-num rid="cn002">62176140</contract-num>
<contract-num rid="cn002">82001775</contract-num>
<contract-num rid="cn003">20JR5RA292</contract-num>
<contract-num rid="cn004">20BSH151</contract-num>
<contract-num rid="cn005">ZR2020MG013</contract-num>
<contract-num rid="cn005">ZR2021MH120</contract-num>
<contract-sponsor id="cn001">National Key Research and Development Program of China<named-content content-type="fundref-id">10.13039/501100012166</named-content></contract-sponsor>
<contract-sponsor id="cn002">National Natural Science Foundation of China<named-content content-type="fundref-id">10.13039/501100001809</named-content></contract-sponsor>
<contract-sponsor id="cn003">Natural Science Foundation of Gansu Province<named-content content-type="fundref-id">10.13039/501100004775</named-content></contract-sponsor>
<contract-sponsor id="cn004">National Social Science Fund of China<named-content content-type="fundref-id">10.13039/501100012456</named-content></contract-sponsor>
<contract-sponsor id="cn005">Natural Science Foundation of Shandong Province<named-content content-type="fundref-id">10.13039/501100007129</named-content></contract-sponsor>
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<ref-count count="63"/>
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</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Rectal cancer (RC) is a disease characterized by a high mortality rate. Patients with RC usually suffer from tremendous psychological stress, which leads to a series of psychological diseases (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>). Some contemporary studies showed that various discomfort symptoms caused by chemotherapy could induce cognitive impairment in patients with cancer, including impaired attention, memory, and executive function (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B4">4</xref>). The long-term emotional distress of the patient increased the risk of depression (<xref ref-type="bibr" rid="B5">5</xref>). Depression-related factors may contribute to the less optimal network topology in the functional network (FN) (<xref ref-type="bibr" rid="B6">6</xref>, <xref ref-type="bibr" rid="B7">7</xref>) and structural network (SN) (<xref ref-type="bibr" rid="B8">8</xref>) of patients with cancer. Neuroimaging studies reported that a considerable number of patients with cancer with surgery and chemotherapy had morphological variation and functional abnormalities in brain, such as decreased hippocampal volume (<xref ref-type="bibr" rid="B9">9</xref>), lower white matter volume (<xref ref-type="bibr" rid="B10">10</xref>), memory difficulties (<xref ref-type="bibr" rid="B1">1</xref>), and cognitive deficit (<xref ref-type="bibr" rid="B11">11</xref>). Therefore, research on FN and SN in this study could bring new insights into the neurophysiological mechanisms in patients with RC, and through the analysis of brain images, the emotional distress of patients with RC could be diagnosed and treated, thereby improving the quality of life of patients (<xref ref-type="bibr" rid="B12">12</xref>).</p>
<p>Combining multimodal data can reveal hidden relationships among different data, unifying different findings in brain imaging (<xref ref-type="bibr" rid="B13">13</xref>). Therefore, multimodal imaging is a prominent method in cognitive neuroscience research. Graph-based functional and structural brain connectivity analysis is a new method, which provides evidence for the complexity of the brain by modeling the interactions between different brain regions (<xref ref-type="bibr" rid="B14">14</xref>, <xref ref-type="bibr" rid="B15">15</xref>). Previous studies have consistently shown that the brain functional network is organized in a small-worldness property, with local specialization and high global information transmission capabilities (<xref ref-type="bibr" rid="B16">16</xref>, <xref ref-type="bibr" rid="B17">17</xref>). Bruno et al. (<xref ref-type="bibr" rid="B1">1</xref>) reported significantly reduced shortest path length and small-worldness property in the breast cancer group. Several findings point that the functional network of patients with cancer loses its ability to support various cognitive functions following chemotherapy (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>). Observational studies found that alterations in brain structural network had an adverse impact on the cognition of cancer survivors (<xref ref-type="bibr" rid="B20">20</xref>, <xref ref-type="bibr" rid="B21">21</xref>). Although there are many studies on brain cognitive impairment in patients with cancer, less is known about FN and SN abnormalities in patients with RC. We used multimodal neuroimaging to investigate the alterations in FCs and SCs for gaining insight into the brain cognitive dysfunction in patients with RC.</p>
<p>In view of the poor understanding of psychological disorders and cognitive impairment of RC survivors in existing studies, it is essential to study the depression tendency and related factors in patients with RC. Therefore, this study investigated the abnormalities in FN and SN using graph theory analysis in patients with RC with surgery and chemotherapy characterized by depression tendency compared with healthy controls (HCs). We hypothesized that patients with RC would show altered small-worldness property and topological architecture in the FN and SN due to the effects of depression tendency. We sought to expand our understanding of the resilience of the brain network in patients with RC. The study also explored the potential association between the significant alterations in network properties of patients with RC and severity of depression symptoms.</p></sec>
<sec sec-type="methods" id="s2">
<title>Methods</title>
<sec>
<title>Participants</title>
<p>A total of 42 patients with RC with surgery and chemotherapy were recruited from the Gansu Provincial Hospital, whereas the 38 age- and gender-matched healthy control participants were recruited through newspaper advertisements. They were recruited from July 2017 to June 2020. All participants were diagnosed according to DSM-IV criteria by two experienced psychiatrists. They have executed the evaluation of 17-item Hamilton Rating Scale for Depression (HAMD-17). The evaluation results showed that all the patients with RC included in the experiment had depression tendency. All participants were given written informed consent when image scanning. None of the subjects took any psychotropic drugs.</p></sec>
<sec>
<title>Data Acquisition</title>
<p>Magnetic resonance imaging data were acquired using a 3.0 T Siemens Trio scanner (Siemens Erlangen, Germany). Subjects were asked to relax with eyes closed and not to think about anything. The structural image was acquired with a T1-weighted spin-echo sequence: TR/TE = 2530/2.98 ms, slice thickness = 1 mm, slice gap = 0.8 mm, FOV = 256<sup>&#x0002A;</sup>256 mm, The resting-state functional images (rs-fMRI) were obtained with the following parameters: TR/TE = 2,000/30 ms, 64<sup>&#x0002A;</sup>64 matrix, FOV = 224<sup>&#x0002A;</sup>224 mm, total 240 volumes, 32 sequential ascending axial slices of 3.5 mm thickness. Diffusion tensor imaging (DTI) data were acquired using a single-shot echo-planar imaging-based sequence with the following parameters: TR = 11,600, TE = 85, FOV = 256 mm <sup>&#x0002A;</sup> 256 mm, acquisition matrix = 112<sup>&#x0002A;</sup>112, axial slices = 32, 64 diffusion directions with b = 1,000 s/mm<sup>2</sup>, and an additional image without b = 0 s/mm<sup>2</sup>.</p></sec>
<sec>
<title>Data Processing</title>
<p>We used the SPM8 (Statistical Parametric Mapping: <ext-link ext-link-type="uri" xlink:href="http://www.fil.ion.ucl.ac.uk/spm">http://www.fil.ion.ucl.ac.uk/spm</ext-link>) and DPARSFA (Data Processing Assistant Resting-State: <ext-link ext-link-type="uri" xlink:href="http://www.restfmri.net">http://www.restfmri.net</ext-link>) on the preprocessing of all the rs-fMRI data (<xref ref-type="bibr" rid="B22">22</xref>). The specific preprocessed steps were as follows: (1) the first 10 volumes of the fMRI were removed; (2) we performed the slice timing, head movement correction, and rearrangement; (3) all subjects were excluded if their head motion which was &#x0003E;2.0 mm maximum displacement in any of the x, y, or z directions was &#x0003E;2&#x000B0; (<xref ref-type="bibr" rid="B23">23</xref>); (4) all the rs-fMRI data were spatially normalized to the Montreal Neurological Institute (MNI) space using structural image normalization parameters; (5) the smoothing Gaussian kernel of full width at half maximum (FWHM) was 8 mm (<xref ref-type="bibr" rid="B24">24</xref>); (6) the 24 head motion parameters, averaged global, white matter signals, and cerebrospinal fluid were processed by nuisance covariates regression (<xref ref-type="bibr" rid="B25">25</xref>); (7) removing linear trends; and (8) temporal band-pass filtering (0.01&#x02013;0.08 Hz) (<xref ref-type="bibr" rid="B26">26</xref>).</p>
<p>The DTI data were preprocessed using PANDA (<ext-link ext-link-type="uri" xlink:href="http://www.nitrc.org/projects/panda">http://www.nitrc.org/projects/panda</ext-link>) (<xref ref-type="bibr" rid="B27">27</xref>) in MATLAB2014a. The specific preprocessed steps were as follows: in MATLAB2014a. (1) converting DICOM files into NIfTI images; (2) estimating the brain mask; (3) cropped the image; (4) correction of the eddy current effect and head motions; (5) averaging multiple acquisitions; and (7) FA metrics calculation.</p></sec>
<sec>
<title>Construction of Brain Networks</title>
<p>The Human Brainnetome Atlas (246 Atlas) were used to demarcate the nodes and edges of the brain network (<xref ref-type="bibr" rid="B28">28</xref>). In each subject, 246 atlas were used to construct brain networks for further graph theory analysis.</p>
<p>The GRETNA (a toolbox for analyzing brain network, <ext-link ext-link-type="uri" xlink:href="http://www.nitrc.org/projects/gretna/">www.nitrc.org/projects/gretna/</ext-link>) were used to construct the functional brain network. For each subject, Pearson correlation coefficient was used to construct the correlation matrix which the mean time series of each region was represented each node. Fisher Z transform was applied to each matrix to convert the data into Z-scores. A FA-weighted symmetric matrix was constructed for each participant by deterministic tractography as the following analysis basis. Each matrix represented the white matter network of the cerebral cortex, and each row or column in network represented the brain region of 246 atlas.</p></sec>
<sec>
<title>Threshold Calculation</title>
<p>To construct an undirected binary network and make the generated graph metrics stable, it is necessary to be thresholded for the weight of the brain networks. There is no fixed method to determine the threshold in current research. Therefore, in FN, we used sparsity (26&#x02013;50%) with a step of 1% (<xref ref-type="bibr" rid="B29">29</xref>) to divide the network threshold. Then, we calculated the topological properties of FN in a series of threshold range. In SN, we use FA (0.20.42) with a step of 0.2 as the threshold of the network according to the previous study (<xref ref-type="bibr" rid="B30">30</xref>). The small-worldness property is related to the threshold of the network (<xref ref-type="bibr" rid="B31">31</xref>), so we need to calculate a network threshold to get effective network properties.</p></sec>
<sec>
<title>Whole Brain Network Organization</title>
<p>Graph theoretical analyses of the FN and SN in patients with RC and HC were calculated with routines from the GRETNA toolbox. The network topological properties at the global levels were calculated, including (1) properties that suggest network segregation of brain, such as the normalized clustering coefficient (&#x003B3;), the local efficiency <italic>E</italic><sub><italic>loc</italic></sub>(<italic>G</italic>); (2) properties that indicate network integration of the brain, such as the normalized shortest path length(&#x003BB;), the global efficiency <italic>E</italic><sub><italic>glob</italic></sub>(<italic>G</italic>); (3) small-worldness (&#x003B4;) property which evaluates the balance of segregation and integration.</p>
<p>The nodal efficiency (<italic>E</italic><sub><italic>nod</italic></sub>) measures the ability of a particular node to propagate information with all other nodes in the network. It is considered as the inverse of the harmonic mean of the minimum path length between an index node and all other nodes in the network.</p></sec>
<sec>
<title>Network Resilience Analysis</title>
<p>Network resilience refers to the ability to withstand perturbations or failures in the network, which is usually related to the stability of complex networks (<xref ref-type="bibr" rid="B32">32</xref>, <xref ref-type="bibr" rid="B33">33</xref>). In FN and SN, we used random or targeted attacks with fixed sparsity or FA values to evaluate the network resilience, so as to ensure that all anatomical regions were involved in the network, thus minimizing the number of false-positive paths (<xref ref-type="bibr" rid="B32">32</xref>). In targeted attack analysis, the betweenness value of each node in the network was calculated and sorted in descending order. We deleted the nodes in the network in order of betweenness value and calculated the global efficiency of each network after attack (<xref ref-type="bibr" rid="B34">34</xref>). In random attack analysis, we deleted the nodes of network randomly and calculated the global efficiency of each network after attack.</p></sec>
<sec>
<title>Statistical Analysis</title>
<p>The demographic and clinical characteristics of the patients with RC and HC were analyzed by chi-square test and two-sample <italic>t</italic>-tests using SPSS 21. We performed statistical comparisons of topological measures between the two groups using non-parametric permutation tests with 5,000 iterations for each sparsity and FA value (<xref ref-type="bibr" rid="B35">35</xref>). For the <italic>E</italic><sub><italic>nod</italic></sub>, the non-parametric permutation tests was repeated at the sparsity = 26% and the FA value = 0.42. FDR correction was conducted for all these results. Besides, we used Pearson correlation analyses to explore the correlations in patients with RC between nodes with significant difference in <italic>E</italic><sub><italic>nod</italic></sub> and the severity of depression (HAMD score).</p></sec></sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>Demographic Characteristics</title>
<p>Demographic information is summarized in <xref ref-type="table" rid="T1">Table 1</xref>. There is no significant difference in age (<italic>p</italic> = 0.564) and gender (&#x003C7;<sup>2</sup> =1.312, <italic>p</italic> = 0.765) between the two groups. There was a significant difference in HAMD score between the two groups (<italic>p</italic> &#x0003C; 0.001).</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>Demographic and clinical characteristics of subjects.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Variables (Mean &#x000B1;SD)</bold></th>
<th valign="top" align="center"><bold>Patients with RC</bold><break/><bold>(<italic>n</italic> &#x0003D; 42)</bold></th>
<th valign="top" align="center"><bold>Healthy controls</bold><break/><bold>(<italic>n</italic> &#x0003D; 38)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Gender (M:F)</td>
<td valign="top" align="center">23:19</td>
<td valign="top" align="center">22:16</td>
<td valign="top" align="center">0.564&#x00023;</td>
</tr>
<tr>
<td valign="top" align="left">Age (years)</td>
<td valign="top" align="center">50.89 &#x000B1; 7.50</td>
<td valign="top" align="center">48.96 &#x000B1; 7.93</td>
<td valign="top" align="center">0.756&#x0002A;</td>
</tr>
<tr>
<td valign="top" align="left">HAMD</td>
<td valign="top" align="center">9.94 &#x000B1; 4.93</td>
<td valign="top" align="center">_</td>
<td valign="top" align="center">_</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>SD, standard deviation; HAMD, Hamilton depression rating scale</italic>.</p>
<p><italic><sup>&#x00023;</sup> and</italic></p>
<p><italic><sup>&#x0002A;</sup> indicate p-value for chi-square test and two-sample t-test, respectively</italic>.</p>
</table-wrap-foot>
</table-wrap></sec>
<sec>
<title>The Alterations of FN and SN Properties</title>
<p>In the functional network, patients with RC have a higher shortest path length (&#x003BB;) than HC (<xref ref-type="fig" rid="F1">Figure 1B</xref>, sparsity = 26%). Since there is no significant difference in the clustering coefficient (&#x003B3;) between the two groups under the same sparsity (<xref ref-type="fig" rid="F1">Figure 1A</xref>), this leads to the abnormal small-worldness(&#x003C3;) (<xref ref-type="fig" rid="F1">Figure 1C</xref>) of patients with RC. The local efficiency has increased in patients with RC (<xref ref-type="fig" rid="F1">Figure 1D</xref>, sparsity = 26%), and there is no significant change in global efficiency (<xref ref-type="fig" rid="F1">Figure 1E</xref>).</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption><p>Functional connectivity network at different sparsity for patients with RC (the blue line) and controls (the pink line) and their statistical comparison results (<italic>p</italic> &#x0003C; 0.05 5,000 permutation test, FDR correction). <bold>(A)</bold> Gamma, <bold>(B)</bold> lambda, <bold>(C)</bold> sigma, <bold>(D)</bold> local efficiency, and <bold>(E)</bold> global efficiency. The black triangles indicate a significant group difference.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fneur-13-791298-g0001.tif"/>
</fig>
<p>In the structural network, the clustering coefficient (&#x003B3;) (<xref ref-type="fig" rid="F2">Figure 2A</xref>, FA = 0.32) and small-worldness(&#x003C3;) (<xref ref-type="fig" rid="F2">Figure 2C</xref>, FA = 0.32, 0.34, and 0.38) of patients with RC is larger than that of HC, the shortest path length (&#x003BB;) (<xref ref-type="fig" rid="F1">Figure 1B</xref>) being unchanged. In addition, compared with HC, the global efficiency of patients with RC has increased (<xref ref-type="fig" rid="F2">Figure 2E</xref>, FA = 0.28&#x02013;0.32).</p>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption><p>Structural connectivity network at different FA threshold for RC (the blue line) and controls (the pink line) and their statistical comparison results (<italic>p</italic> &#x0003C; 0.05 5000 permutation test, FDR correction). <bold>(A)</bold> Gamma, <bold>(B)</bold> lambda, <bold>(C)</bold> sigma, <bold>(D)</bold> local efficiency, and <bold>(E)</bold> global efficiency. The black triangles indicate a significant group difference.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fneur-13-791298-g0002.tif"/>
</fig></sec>
<sec>
<title>Regional Efficiency Comparison</title>
<p>In FN, patients with RC showed that significantly decreased nodal efficiency. There were several regions including bilateral basal ganglia, right parahippocampal gyrus, bilateral thalamus, right precuneus, and right lateral occipital cortex. Meanwhile, the increased nodal efficiency was mainly in frontal lobe (orbital gyrus), basal ganglia, left inferior frontal gyrus, left amygdala, bilateral cingulate gyrus, left inferior parietal lobule, and right precentral gyrus in FN and SN for patients with RC (<italic>p</italic> &#x0003C; 0.05, after 5,000 permutation test, FDR test) (<xref ref-type="table" rid="T2">Tables 2</xref>, <xref ref-type="table" rid="T3">3</xref>; <xref ref-type="fig" rid="F3">Figure 3</xref>).</p>
<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption><p>Brain regions with significant group effect in the nodal efficiency between patients with RC and HC for FN.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th/>
<th valign="top" align="left"><bold>Regions</bold></th>
<th valign="top" align="center"><bold>Patients with RC</bold></th>
<th valign="top" align="center"><bold>Control</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><bold>RC</bold> <bold>&#x0003C;</bold> <bold>HC</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">vmPu.R</td>
<td valign="top" align="center">0.5580 &#x000B1; 0.0582</td>
<td valign="top" align="center">0.6190 &#x000B1; 0.0578</td>
<td valign="top" align="center">0.0002</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">dCa.L</td>
<td valign="top" align="center">0.5116 &#x000B1; 0.0694</td>
<td valign="top" align="center">0.5816 &#x000B1; 0.0592</td>
<td valign="top" align="center">0.0002</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">GP.R</td>
<td valign="top" align="center">0.5575 &#x000B1; 0.0732</td>
<td valign="top" align="center">0.6195 &#x000B1; 0.0526</td>
<td valign="top" align="center">0.0002</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">vmPu.L</td>
<td valign="top" align="center">0.5765 &#x000B1; 0.0490</td>
<td valign="top" align="center">0.6264 &#x000B1; 0.0542</td>
<td valign="top" align="center">0.0002</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">TL.R</td>
<td valign="top" align="center">0.5874 &#x000B1; 0.0466</td>
<td valign="top" align="center">0.5941 &#x000B1; 0.0533</td>
<td valign="top" align="center">0.0008</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">PPtha.R</td>
<td valign="top" align="center">0.5245 &#x000B1; 0.0737</td>
<td valign="top" align="center">0.5846 &#x000B1; 0.0519</td>
<td valign="top" align="center">0.0004</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">GP.L</td>
<td valign="top" align="center">0.5581 &#x000B1; 0.0661</td>
<td valign="top" align="center">0.6107 &#x000B1; 0.0620</td>
<td valign="top" align="center">0.0006</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">lPFtha.R</td>
<td valign="top" align="center">0.5645 &#x000B1; 0.0698</td>
<td valign="top" align="center">0.6148 &#x000B1; 0.0589</td>
<td valign="top" align="center">0.0032</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">vCa.R</td>
<td valign="top" align="center">0.5223 &#x000B1; 0.0507</td>
<td valign="top" align="center">0.5645 &#x000B1; 0.0514</td>
<td valign="top" align="center">0.0044</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A7m.R</td>
<td valign="top" align="center">0.6101 &#x000B1; 0.0540</td>
<td valign="top" align="center">0.6404 &#x000B1; 0.0656</td>
<td valign="top" align="center">0.0060</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Otha.R</td>
<td valign="top" align="center">0.5318 &#x000B1; 0.0491</td>
<td valign="top" align="center">0.5833 &#x000B1; 0.0610</td>
<td valign="top" align="center">0.0052</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">mPMtha.R</td>
<td valign="top" align="center">0.5719 &#x000B1; 0.0416</td>
<td valign="top" align="center">0.6158 &#x000B1; 0.0542</td>
<td valign="top" align="center">0.0060</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">msOccG.R</td>
<td valign="top" align="center">0.6029 &#x000B1; 0.0705</td>
<td valign="top" align="center">0.6429 &#x000B1; 0.0569</td>
<td valign="top" align="center">0.0098</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">dCa.R</td>
<td valign="top" align="center">0.5286 &#x000B1; 0.0650</td>
<td valign="top" align="center">0.5701 &#x000B1; 0.0647</td>
<td valign="top" align="center">0.0090</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">mPFtha.R</td>
<td valign="top" align="center">0.5545 &#x000B1; 0.0615</td>
<td valign="top" align="center">0.6007 &#x000B1; 0.0778</td>
<td valign="top" align="center">0.0090</td>
</tr>
<tr>
<td valign="top" align="left"><bold>RC</bold> <bold>&#x0003E;</bold> <bold>HC</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A23v.L</td>
<td valign="top" align="center">0.6719 &#x000B1; 0.0485</td>
<td valign="top" align="center">0.6601 &#x000B1; 0.0612</td>
<td valign="top" align="center">0.0018</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A40rd.L</td>
<td valign="top" align="center">0.6862 &#x000B1; 0.0527</td>
<td valign="top" align="center">0.6738 &#x000B1; 0.0686</td>
<td valign="top" align="center">0.0042</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A40rv.L</td>
<td valign="top" align="center">0.7195 &#x000B1; 0.0408</td>
<td valign="top" align="center">0.6875 &#x000B1; 0.0388</td>
<td valign="top" align="center">0.0048</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A23v,R</td>
<td valign="top" align="center">0.6742 &#x000B1; 0.0394</td>
<td valign="top" align="center">0.6360 &#x000B1; 0.0479</td>
<td valign="top" align="center">0.0064</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A4tl.R</td>
<td valign="top" align="center">0.7038 &#x000B1; 0.0857</td>
<td valign="top" align="center">0.6709 &#x000B1; 0.0631</td>
<td valign="top" align="center">0.0048</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>vmPu, ventromedial putamen; dCa, dorsal caudate; GP, globus pallidus; TL, area TL (lateral PPHC, posterior parahippocampal gyrus); PPtha, posterior parietal thalamus; lPFtha, lateral prefrontal thalamus; vCa, ventral caudate; A7m, medial area 7(PEp); Otha, occipital thalamus; mPMtha, pre-motor thalamus; msOccG, medial superior occipital gyrus; mPFtha, medial prefrontal thalamus; L, left; R, right</italic>.</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="T3">
<label>Table 3</label>
<caption><p>Brain regions with significant group effect in the nodal efficiency between patients with RC and HC for SN.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th/>
<th valign="top" align="left"><bold>Regions</bold></th>
<th valign="top" align="center"><bold>Patients with RC</bold></th>
<th valign="top" align="center"><bold>Control</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left" colspan="5"><bold>RC</bold> <bold>&#x0003E;</bold> <bold>HC</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A12/47l.L</td>
<td valign="top" align="center">0.2498 &#x000B1; 0.0352</td>
<td valign="top" align="center">0.2099 &#x000B1; 0.0717</td>
<td valign="top" align="center">0.0036</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">dlPu.L</td>
<td valign="top" align="center">0.3117 &#x000B1; 0.0386</td>
<td valign="top" align="center">0.2774 &#x000B1; 0.0610</td>
<td valign="top" align="center">0.0036</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A44op.L</td>
<td valign="top" align="center">0.2461 &#x000B1; 0.0316</td>
<td valign="top" align="center">0.2105 &#x000B1; 0.0698</td>
<td valign="top" align="center">0.0054</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">A32sg.L</td>
<td valign="top" align="center">0.2365 &#x000B1; 0.0365</td>
<td valign="top" align="center">0.1857 &#x000B1; 0.0993</td>
<td valign="top" align="center">0.0062</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">LAmyg.L</td>
<td valign="top" align="center">0.2589 &#x000B1; 0.0269</td>
<td valign="top" align="center">0.2148 &#x000B1; 0.0923</td>
<td valign="top" align="center">0.0086</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>A12/47l, lateral area 12/47; dlPu, dorsolateral putamen; A44op, opercular area 44; A32sg, subgenual area 32; LAmyg, lateral amygdala; L, left; R, right</italic>.</p>
</table-wrap-foot>
</table-wrap>
<fig id="F3" position="float">
<label>Figure 3</label>
<caption><p>Regions with significant differences in nodal efficiency between patients with RC and HC. Nonparametric permutation tests were applied to nodal efficiency of all 246 cortical regions (<italic>p</italic> &#x0003C; 0.05; 5,000 permutation test, FDR correction). <bold>(A)</bold> Represented FN, and <bold>(B)</bold> represented SN. Red is for increased nodal efficiency in RC patients group, while blue is for decreased nodal efficiency in RC patients group. L, left; R, right.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fneur-13-791298-g0003.tif"/>
</fig></sec>
<sec>
<title>The Analysis of Network Resilience</title>
<p>With the targeted and random attack, a significantly decreased decline of the global efficiency was found in FN and SN (<xref ref-type="fig" rid="F4">Figure 4</xref>). In both networks, the global efficiency of patients with RC decreased faster over a wide percentage of removal, which reflected that the networks of patients with RC were more fragile. In all subjects, the resilience of structural network is weaker than that of functional network under the same threshold.</p>
<fig id="F4" position="float">
<label>Figure 4</label>
<caption><p>Network resilience under random and target analysis. The alterations of global efficiency under removing node at random (first panel) and targeted pattern (second panel). The blue line corresponded to the performance of HC, pink line for RC. The <bold>(A,C)</bold> were for FN and the <bold>(B,D)</bold> were for SN.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fneur-13-791298-g0004.tif"/>
</fig></sec>
<sec>
<title>Correlations Between Network Properties and HAMD Scores for RC</title>
<p>In the analysis, there were correlations between the HAMD score and the nodes with significant <italic>E</italic><sub><italic>nod</italic></sub> in the FN. For FN, mPMtha.R (r = 0.389, <italic>p</italic> = 0.023) (<xref ref-type="fig" rid="F5">Figure 5B</xref>), and for SN, LAmyg.L (r = 0.440, <italic>p</italic> = 0.01) (<xref ref-type="fig" rid="F5">Figure 5A</xref>).</p>
<fig id="F5" position="float">
<label>Figure 5</label>
<caption><p><bold>(A,B)</bold> The nodal efficiency of several regions was positively correlated with the HAMD score for FN and SN. The brain map showed regions with decreased <italic>E</italic><sub><italic>nod</italic></sub>(Blue for mPMtha.R and pink for LAmyg.L). mPFtha, medial prefrontal thalamus; LAmyg, lateral amygdala; L, left; R, right.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fneur-13-791298-g0005.tif"/>
</fig></sec></sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>In this study, different topological organizations of FN and SN in patients with RC and HC were explored. The findings pointed patients with RC displayed altered small-worldness property and global topological organization compared with HC. Moreover, there were regions with significant abnormal <italic>E</italic><sub><italic>nod</italic></sub> being mainly distributed in frontal region, subcortical regions, and central region in patients with RC. In addition, patients with RC showed vulnerable network resilience in both networks, and FN would be more stable than SN across participants.</p>
<sec>
<title>Network Properties</title>
<p>Many studies have used fMRI (<xref ref-type="bibr" rid="B36">36</xref>, <xref ref-type="bibr" rid="B37">37</xref>) and DTI (<xref ref-type="bibr" rid="B21">21</xref>) images to explore the global and regional brain network properties of patients with breast cancer and lung cancer, but there are still few studies on rectal cancer. Compared with HC, the functional networks of patients with RC displayed a higher shortest path length (&#x003BB;) and decreased small-worldness(&#x003C3;), reflecting reduced global integration and disrupted organization balance (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B21">21</xref>). Our results also revealed increased local efficiency in patients with RC. It is a measure of local information transmission among adjacent nodes and therefore an indication of network segregation (<xref ref-type="bibr" rid="B38">38</xref>, <xref ref-type="bibr" rid="B39">39</xref>). Previous studies demonstrated reduced local efficiency, a common measure of the brain network&#x00027;s response to computational attack, associated with patients with breast cancer (<xref ref-type="bibr" rid="B21">21</xref>, <xref ref-type="bibr" rid="B40">40</xref>). Due to brain structural damage, decreased local efficiency would affect the fault tolerant ability of brain network. More detail, the result of weakening network fault tolerance is that if a node in the brain is damaged, the connection between previously linked nodes would be greatly affected (<xref ref-type="bibr" rid="B41">41</xref>). Therefore, reduced local efficiency is a risk factor for patients with RC. Recently, researchers use graph theory to analyze complex brain functional networks after chemotherapy. It has been proved that chemotherapy-related cognitive deficits were associated with abnormal topological alterations of brain functional and structural network (<xref ref-type="bibr" rid="B42">42</xref>, <xref ref-type="bibr" rid="B43">43</xref>). In this study, increased shortest path length and decreased local efficiency in patients with RC with surgery and chemotherapy could be seen as a brain compensation mechanism, which included changing the global pathway and adjusting regional activity to preserve a seesaw-like balance of the brain network.</p>
<p>Patients with RC showed increased clustering coefficients (&#x003B3;), small-worldness(&#x003C3;), and global efficiency in SN (<xref ref-type="fig" rid="F2">Figure 2</xref>). Abnormal small-worldness property of SN indicated that the local specialization and global integration of brain in patients with RC were disrupted, where the SN tended to be more randomized (<xref ref-type="bibr" rid="B44">44</xref>). Global efficiency is the inverse of the average shortest path between nodes. When nodes could interact directly, the efficiency is high (<xref ref-type="bibr" rid="B21">21</xref>). Therefore, global efficiency is an indicator of network function integration and parallel information processing capability (<xref ref-type="bibr" rid="B41">41</xref>). The present results of abnormal network properties reflected the undesired topological organization in SN, which exhibited that the deficits of emotional and cognitive processing in patients with RC might result from network damages. Besides, the increased network properties of SN in patients with RC might suggest that local nerve fibers reconstructed in response to the abnormalities in brain functional network. The compensatory response of the SN is activated for maintaining brain functional integrity to compensate the cognitive impairment caused by chemotherapy to patients with RC (<xref ref-type="bibr" rid="B24">24</xref>). Aforementioned evidence illuminated that cognitive deficit related to patients with RC may act <italic>via</italic> disrupted coordination between global and regional networks.</p></sec>
<sec>
<title>Nodal Efficiency of Networks</title>
<p>To explore the functional and structural characteristics of the human brain more accurately and quantitatively, our study employed a new standard brain atlas, containing 246 brain regions. This atlas would allow brain network analysis to use predefined nodes in an informed manner (<xref ref-type="bibr" rid="B45">45</xref>). Therefore, more detailed division of brain regions provides better help in multimodal data analysis. We observed decreased <italic>E</italic><sub><italic>nod</italic></sub> only in FN of patients with RC. The significantly changed regions were located in bilateral basal ganglia, bilateral thalamus, right parahippocampal gyrus, right precuneus, and right lateral occipital cortex. The basal ganglia is not only related to motor control, but also related to the cognitive and limbic functions (<xref ref-type="bibr" rid="B45">45</xref>). Moreover, basal ganglia is the collection of subcortical nuclei surrounding the thalamus (<xref ref-type="bibr" rid="B46">46</xref>). Abnormal activation of basal ganglia/thalamus was found in the depressive studies (<xref ref-type="bibr" rid="B47">47</xref>), suggesting that abnormalities in these brain regions may lead to abnormal emotional processing mechanisms. Prior studies reported that parahippocampal gyrus and precuneus were associated with memory function, so alterations in these regions might affect memory decline (<xref ref-type="bibr" rid="B48">48</xref>, <xref ref-type="bibr" rid="B49">49</xref>). Task fMRI study of memory factors found that the occipital cortex of patients with cancer was more significantly correlated with vigor and fatigue scores (<xref ref-type="bibr" rid="B50">50</xref>). Frequent fatigue is a common symptom of patients with cancer (<xref ref-type="bibr" rid="B51">51</xref>). Aforementioned evidence indicated that the decreased <italic>E</italic><sub><italic>nod</italic></sub> of FN in this study represented alterations in regional characteristics of the brain network, which further affected the cognitive impairment of patients with RC.</p>
<p>Furthermore, the increased nodal efficiency was mainly in frontal cortex, left amygdala, bilateral cingulate gyrus, left inferior parietal lobule, and right precentral gyrus in FN and SN for patients with RC. In experiments with high-demand condition, the right inferior frontal gyrus and other components of the two hemisphere working memory circuitry in patients with cancer were found greater activation than the control group in a prior study (<xref ref-type="bibr" rid="B52">52</xref>). These abnormalities might be a compensation mechanism to preserve normal thinking and responsiveness in patients with cancer. In addition, chemotherapy affects estrogen levels in patients with cancer. Estrogen levels are thought to have neuroprotective effects in the brain, thus helping to maintain cognitive function (<xref ref-type="bibr" rid="B53">53</xref>). Therefore, female patients with cancer are more likely to develop cognitive impairment in brain regions related to learning and memory after chemotherapy, such as hippocampus and amygdala (<xref ref-type="bibr" rid="B54">54</xref>). The anterior cingulate cortex is involved in attention control, response selection, and error monitoring (<xref ref-type="bibr" rid="B55">55</xref>). Abnormal brain activity patterns in the attention-controlled regions, including the anterior cingulate gyrus, are related to anxiety (<xref ref-type="bibr" rid="B56">56</xref>). The emotional fluctuation caused by excessive psychological stress in patients with RC could induce abnormal activation of cingulate gyrus. Saykin et al. (<xref ref-type="bibr" rid="B57">57</xref>) revealed that the activation of frontal and parietal lobes increased during the speech working memory task 1 month after chemotherapy. Compared with controls, the cancer group showed significantly greater activation in right precentral gyrus and right cingulate gyrus (<xref ref-type="bibr" rid="B19">19</xref>). Moreover, in the SN, the nodal efficiency was only increased. We speculated that after surgery and chemotherapy, the node efficiency of SN showed more obvious activation to maintain the robustness of overall network at the expense of other network property, such as integration. These results improved the understanding of chemotherapy-induced cognitive impairment in patients with RC from the perspective of brain node efficiency.</p>
<p>As shown in <xref ref-type="fig" rid="F5">Figure 5</xref>, the patients with RC showed a positive relationship between HAMD and decreased nodal efficiency in mPMtha.R of FN, as well as a positive relationship between HAMD and increased nodal efficiency in LAmyg.L of SN. The correlation between the changed node efficiency and HAMD score may indicate impaired cognitive control combined with abnormal affective processing in patients with RC (<xref ref-type="bibr" rid="B29">29</xref>). A prior study suggested that regions sensitive to negative emotions were hyperactive in processing negative information (<xref ref-type="bibr" rid="B36">36</xref>), and it was not surprising to find a significant positive correlation between increased nodal efficiency and HAMD in the amygdala. Moreover, the positive relationship between HAMD and decreased nodal efficiency revealed that abnormal activation of FN in patients with RC might cause cognitive impairments and depressed mood (<xref ref-type="bibr" rid="B58">58</xref>). Therefore, we speculated that alterations in brain network properties assist us to study the depression tendency in patients with RC after chemotherapy and surgery.</p></sec>
<sec>
<title>Comparison of Network Resilience</title>
<p>In both networks, a key finding of significantly decreased resilience to targeted and random attack was found (<xref ref-type="fig" rid="F4">Figure 4</xref>). Being more effective than other network properties to measure network integration performance, global efficiency of the FN and SN was utilized to explore network resilience quantitatively (<xref ref-type="bibr" rid="B34">34</xref>). In this study, both networks of patients with RC were more vulnerable and SN is less resilient than FN, which were consistent with our previous research results (<xref ref-type="bibr" rid="B59">59</xref>). This finding enhanced the conclusion that lower brain resilience was associated with progressive deterioration of cognitive impairment in breast cancer survivors (<xref ref-type="bibr" rid="B21">21</xref>). Similar results were investigated in other neurological diseases such as major depressive disorders (<xref ref-type="bibr" rid="B33">33</xref>) and temporal lobe epilepsy (<xref ref-type="bibr" rid="B32">32</xref>). A previous study showed that the degree distribution of brain network followed the exponentially truncated power law (<xref ref-type="bibr" rid="B60">60</xref>). This exponentially truncated power law distribution may be helpful in resisting the targeted attack of the hubs, which means that the brain networks of two groups were almost constant when deletion rate was low (<xref ref-type="bibr" rid="B61">61</xref>). The deletion ratios reaching 50%, and the decline rate of global efficiency in networks began to exhibit obvious differences. Exploring the resilient of networks actually simulated the process of cognitive decline in all participants. In detail, as the important nodes were deleted, the functional and structural integrity of brain networks were impaired. Additionally, the FN was more resilient than the SN this study, which were similar to these findings in the previous studies (<xref ref-type="bibr" rid="B30">30</xref>, <xref ref-type="bibr" rid="B62">62</xref>). A prior study discovered that there was commonly a functional connectivity between regions that have no direct structural connectivity, implying that functional network was a more stable system in brain network (<xref ref-type="bibr" rid="B63">63</xref>). Therefore, functional networks were more robust to node removal. Our results may provide a new direction for studying cognitive impairment in patients with RC after surgery and chemotherapy.</p></sec></sec>
<sec sec-type="conclusions" id="s5">
<title>Conclusion</title>
<p>This study explores the effects of depression tendency on brain functional and structural network in patients with RC with surgery and chemotherapy through multimodal brain connectivity analysis. Patients with RC show the abnormal small-worldness property and network topological organization in FN and SN. The alterations in nodal parameter are mainly observed in the limbic and parietal lobes as well as the subcortical nuclei in patients with RC. The patients with RC demonstrate significant cognitive impairment compared with HC, and this impairment may be associated with lower network attack tolerance. The discovery of functional and structural networks is critical for understanding the neurobiological mechanism associated with depression tendency in patients with RC with surgery and chemotherapy.</p></sec>
<sec id="s6">
<title>Limitation</title>
<p>The lack of follow-up data limited the ability of studying the causal relationship between alterations in brain network and depression tendency of patients with RC. The statistical power is restricted by small sample size to some extent. Finally, this study lacks the joint analysis for multimodal data. It is very meaningful to use different modal data for fusion research.</p></sec>
<sec sec-type="data-availability" id="s7">
<title>Data Availability Statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p></sec>
<sec id="s8">
<title>Ethics Statement</title>
<p>The studies involving human participants were reviewed and approved by Medical Ethics Committee of Gansu Provincial People&#x00027;s Hospital. The patients/participants provided their written informed consent to participate in this study.</p></sec>
<sec id="s9">
<title>Author Contributions</title>
<p>Conceived and designed the experiments: WZ, YZ, FZ, NM, GH, ZY, and BH. Analyzed the data and wrote the paper: WZ, YY, and YZ. Contributed reagents/materials/analysis tools: WZ, YZ, YL, GH, ZY, and BH. All authors contributed to and have approved the final manuscript.</p></sec>
<sec sec-type="funding-information" id="s10">
<title>Funding</title>
<p>This work was supported in part by the National Key Research and Development Program of China (Grant No. 2019YFA0706200), in part by the National Key Research and Development Program of China (Grant No. 2016YFC1307203), in part by the National Natural Science Foundation of China (Grant Nos. 61632014, 61627808, 62176140, and 82001775), in part by the Natural Science Foundation of Gansu Province of China (Grant No. 20JR5RA292), and in part by the Department of Education of Gansu Province: Innovation Star Project for Excellent Postgraduates (2021CXZX-121), in part by Gansu Provincial Hospital Youth Research Fund Project, 18GSSY5-5, in part by the Natural Science Foundation of Shandong Provincial of China (Grant Nos. ZR2021MH120 and ZR2020MG013), in part by the National Social Science Foundation of China (Grant No. 20BSH151), in part by Special Fund of Shandong Medical Association (YXH2021ZX055), in part by the Doctoral Scientific Research Foundation of Shandong Technology and Business University (Grant No. BS 202016), in part of Horizontal project of Yantai Vocational College (No. HX2021041).</p></sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of Interest</title>
<p>The 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 sec-type="disclaimer" id="s11">
<title>Publisher&#x00027;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>
<ack><p>We thank the staff of the Department of Radiology of the Gansu Provincial Hospital for their assistance in collecting the data. We thank all participants for their contributions to this article.</p>
</ack>
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