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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Psychiatry</journal-id>
<journal-title>Frontiers in Psychiatry</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Psychiatry</abbrev-journal-title>
<issn pub-type="epub">1664-0640</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-meta>
<article-id pub-id-type="doi">10.3389/fpsyt.2025.1486835</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Psychiatry</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Improved brain functional network in major depressive disorder with suicidal ideation after individual target-transcranial magnetic stimulation treatment: a graph-theory analysis</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Zhang</surname>
<given-names>Yao</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
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<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Mu</surname>
<given-names>Nan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
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<contrib contrib-type="author">
<name>
<surname>Qi</surname>
<given-names>Shun</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1461508"/>
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<contrib contrib-type="author">
<name>
<surname>Sun</surname>
<given-names>Chuanzhu</given-names>
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<xref ref-type="aff" rid="aff3">
<sup>3</sup>
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<contrib contrib-type="author">
<name>
<surname>Rao</surname>
<given-names>Yang</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
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<contrib contrib-type="author">
<name>
<surname>Yang</surname>
<given-names>Xinyi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Guo</surname>
<given-names>Jianying</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Mu</surname>
<given-names>Yunfeng</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
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<aff id="aff1">
<sup>1</sup>
<institution>Xijing Hospital, Air Force Medical University</institution>, <addr-line>Xi&#x2019;an, Shaanxi</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>The Key Laboratory of Biomedical Information Engineering of Ministry of Education, Institute of Health and Rehabilitation Science, School of Life Science and Technology, The Key Laboratory of Neuro-informatics &amp; Rehabilitation Engineering of Ministry of Civil Affairs, Xi&#x2019;an Jiaotong University</institution>, <addr-line>Xi&#x2019;an</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Shaanxi Brain Modulation and Scientific Research Center</institution>, <addr-line>Xi&#x2019;an, Shaanxi</addr-line>, <country>China</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Gynecological Oncology, Shaanxi Provincial Cancer Hospital</institution>, <addr-line>Xi&#x2019;an</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Andreia Vasconcellos Faria, Johns Hopkins University, United States</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Jie Yang, Central South University, China</p>
<p>Ji-An Li, University of California, San Diego, United States</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Jianying Guo, <email xlink:href="mailto:guojy@fmmu.edu.cn">guojy@fmmu.edu.cn</email>; Yunfeng Mu, <email xlink:href="mailto:837358473@qq.com">837358473@qq.com</email>
</p>
</fn>
<fn fn-type="equal" id="fn003">
<p>&#x2020;These authors have contributed equally to this work and share first authorship</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>22</day>
<month>01</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>16</volume>
<elocation-id>1486835</elocation-id>
<history>
<date date-type="received">
<day>27</day>
<month>08</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>03</day>
<month>01</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Zhang, Mu, Qi, Sun, Rao, Yang, Guo and Mu</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Zhang, Mu, Qi, Sun, Rao, Yang, Guo and Mu</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>
<sec>
<title>Introduction</title>
<p>Major depressive disorder with suicidal ideation (MDD/SI+) is characterized by high prevalence, high recurrence rate, high disability rate and low response rate. There is an urgent need for clarifying the pathogenesis and developing novel treatment methods.</p>
</sec>
<sec>
<title>Methods</title>
<p>Subjects were recruited for the collection of Magnetic Resonance Imaging data and clinical scales. Individual target-transcranial magnetic stimulation (IT-TMS) using Stanford Neuromodulation Therapy over individualized left dorsolateral prefrontal cortex was performed to treat MDD/SI+ with the ethical approval (KY20212218-C-1). GRETNA software was used to analyze brain network characteristics according to graph theory.</p>
</sec>
<sec>
<title>Results</title>
<p>A total of 32 patients (aged 18-55) and 28 healthy controls (aged 20-51) had been recruited. Patients after IT-TMS treatment had significant reduction in suicidal ideation and depressive symptom. The functional network of all three groups conformed to small-world topology. There was a renormalization in topology structure after IT-TMS treatment. Decreased functional connectivity between right insula and left anterior cingulate gyrus correlated with improvement in Beck Scale for Suicide Ideation scores.</p>
</sec>
<sec>
<title>Discussion</title>
<p>The current study highlights that MDD/SI+ patients in this cohort showed abnormal brain network connections compared to healthy controls, and that IT-TMS may exert its treatment effects by reducing spontaneous hyper-connectivity in the salience network and insula.</p>
</sec>
</abstract>
<kwd-group>
<kwd>depression</kwd>
<kwd>suicidal ideation</kwd>
<kwd>transcranial magnetic stimulation</kwd>
<kwd>small-world</kwd>
<kwd>graph-theory</kwd>
</kwd-group>
<counts>
<fig-count count="4"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="29"/>
<page-count count="10"/>
<word-count count="3933"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Neuroimaging</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<title>Introduction</title>
<p>Major depressive disorder (MDD) is the most common mental disorder, characterized by high prevalence, high recurrence rate, high disability rate and low response rate, with 58% MDD patients having suicidal ideation (MDD/SI+) and 15% committing suicide behavior (MDD/SB+) (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>). Although suicide prevention has been thoroughly researched, suicide remains a major cause of morbidity and mortality worldwide, causing a great burden to family and society (<xref ref-type="bibr" rid="B3">3</xref>). Only a few treatment options (e.g., lithium salt, antidepressant and cognitive therapy) are available, but these measures are also accompanied by side effects and unsatisfactory remission rate (<xref ref-type="bibr" rid="B4">4</xref>). Currently, the pathogenesis of MDD/SI+ is still not fully clear. There is an urgent need that clarifies the difference in brain functional networks underlying MDD/SI+ for developing novel treatment methods.</p>
<p>Brain functional networks are complex systems, and multiple connective networks serve different functions (<xref ref-type="bibr" rid="B5">5</xref>&#x2013;<xref ref-type="bibr" rid="B7">7</xref>). For example, Chase et&#xa0;al. found the lower connectivity between the salience network and default mode network in MDD/SI+ patients compared with healthy volunteers (<xref ref-type="bibr" rid="B8">8</xref>). Kim et&#xa0;al. reported that the functional network connectivity between the left superior frontal gyrus and the rest brain regions were significantly reduced in MDD/SI+ patients (<xref ref-type="bibr" rid="B9">9</xref>). These results indicate that abnormality in the widespread functional network might contribute to the pathogenesis of MDD/SI+. Whereas, the functional changes of certain brain networks or regions cannot reflect the brain network mechanism overall. The graph-theory analysis from Magnetic Resonance Imaging (MRI) is to analyze the topology of the whole brain connectomes by calculating the global and local neural network features, which is more suitable for clarifying the potential brain functional differences (<xref ref-type="bibr" rid="B10">10</xref>). Brain networks derived from graph theory, including rich-club (<xref ref-type="bibr" rid="B11">11</xref>) and small-world (<xref ref-type="bibr" rid="B12">12</xref>) networks, are responsible for processing and delivering information efficiently. For example, decreased degree centrality value in a frontoparietal network was found in MDD/SI+ patients that could help distinguish patients from healthy individuals (<xref ref-type="bibr" rid="B13">13</xref>). Among the bipolar disorder patients with high risk of suicide, the dysfunction of hubs, including ventromedial prefrontal cortex and right anterior insula, was found using graph&#x2010;theory analysis (<xref ref-type="bibr" rid="B14">14</xref>). These hubs may be targets for novel therapeutics to reduce suicide risk in bipolar disorder. The connectomics-based functional network alterations in depressed patients with suicidal behavior were also reported (<xref ref-type="bibr" rid="B15">15</xref>). However, graph-theory analysis of whole brain functional connectivity in MDD/SI+ patients is still absent.</p>
<p>If delivered properly, transcranial magnetic stimulation (TMS) can modulate the excitability and plasticity of stimulated regions and other brain parts connected to them (<xref ref-type="bibr" rid="B16">16</xref>). Repetitive TMS (rTMS) has been used with varying degrees of effectiveness in various neurological and psychiatric diseases (<xref ref-type="bibr" rid="B17">17</xref>). For example, rTMS spans six consecutive weeks and meets approximately 32% remission and 49% response in major depression (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>). Another study targeted the left dorsolateral prefrontal cortex (DLPFC) and used rTMS to intervene in six suicidal ideation patients at a dose five times the FDA-approved standard dose, which is named Stanford Neuromodulation Therapy (SNT) (<xref ref-type="bibr" rid="B20">20</xref>). The results showed that after 5 days of treatment, the suicidal ideation score of the 6 patients decreased by 86.27% on average, indicating that rTMS is an efficient and safe intervention option for suicidal ideation. However, the mechanism by which TMS interferes with the brain functional connectivity of suicidal ideation is unknown.</p>
<p>In the current study, we applied SNT as an intervention option for MDD/SI+ patients combined with individual target-transcranial magnetic stimulation (IT-TMS), which represents an innovative tool that opens new avenues in the treatment of mental disorders, especially MDD (<xref ref-type="bibr" rid="B21">21</xref>). We used graph theory to analyze the functional separation and integration, verifying that functional network connectivity and efficiency will be improved after IT-TMS therapy.</p>
</sec>
<sec id="s2" sec-type="materials|methods">
<title>Materials and methods</title>
<sec id="s2_1">
<title>Ethical approval statement</title>
<p>Written informed consent was obtained from the individuals for the publication of any potentially identifiable images or data included in this article. This study was approved by the Research Ethics Review Board of the Institute of Mental Health of Xijing Hospital with the approval number: KY20212218-C-1 in 2021.</p>
</sec>
<sec id="s2_2">
<title>Recruitment</title>
<p>Subjects were recruited from Xijing Hospital from January 2022 to December 2023. All MDD/SI+ patients were made a definite diagnosis using the Diagnostic and Statistical Manual of Mental Disorder. The inclusion criteria were as follows (1): right-handed (2); aged 18-60 (3); 17-item Hamilton Depression Rating Scale (HAMD-17) score &gt;17 and Beck Scale for Suicide Ideation-Chinese Version (BSI-CV) score &gt;6 (4); a negative urine drug screen, and a negative urine pregnancy test if female (5); acute suicide behavior (who needed immediate treatment) was excluded by clinical diagnosis and evaluation. The exclusion was: contraindications of TMS and MRI measurement. For safety, all MDD/SI+ patients were instructed to take venlafaxine or duloxetine constantly according to the doctor&#x2019;s advice. The age- and gender-matched healthy controls (HCs) were also recruited.</p>
</sec>
<sec id="s2_3">
<title>MRI data collection and processing</title>
<p>MRI data were acquired using a 3.0 T UNITED Discovery 770 MRI scanner (Shanghai, China). Subjects were required to keep still, think of nothing, and stay awake during the entire session. The resting-state functional images were obtained with the following parameters: field of view (FOV) = 224 &#xd7; 224 mm, in-plane resolution = 64 &#xd7; 64, echo time (TE) = 30 ms, repetition time (TR) = 2,000 ms, slice thickness = 4 mm, flip angle = 90<sup>&#xb0;</sup> and voxel size = 3.5 &#xd7; 3.5 &#xd7; 4 mm<sup>3</sup>. For anatomical reference, a high-resolution T1-weighted image was also acquired with the following parameters: TR = 7.24 ms, TE = 3.10 ms, FOV = 256 &#xd7; 256 mm, flip angle = 10&#xb0;, slice thickness = 0.5 mm and voxel size = 0.5 &#xd7; 0.5 &#xd7; 1 mm. MRI data were collected before the initiation of TMS treatment (baseline) and immediately after the last TMS treatment in patients&#x2019; group. MRI data of HCs were only collected at baseline.</p>
<p>MRI data were preprocessed using Data Processing and&#xa0;Analysis for Brain imaging (DPABI) software (<ext-link ext-link-type="uri" xlink:href="http://rfmri.org/dpabi">http://rfmri.org/dpabi</ext-link>). The initial 10 volumes were discarded to avoid&#xa0;scanning noise. The remaining images were subjected to slice timing correction and motion realignment (less than 2 mm or 2&#xb0;), during which the mean frame-wise displacement was calculated. Subjects with maximal translation more than 2 mm or&#xa0;maximal rotation more than 2&#xb0; were excluded. Next, to regress&#xa0;out the nuisance signals from cerebrospinal fluid and white matter head motion effects, the Friston-24 model was used. The MRI data were finally normalized to the Montreal Neurological Institute (MNI) space using the diffeomorphic anatomical registration through exponentiated lie algebra (DARTEL) method, smoothed with a Gaussian kernel and band-pass filtered (0.01-0.08 Hz).</p>
</sec>
<sec id="s2_4">
<title>IT-TMS treatment</title>
<p>The individualized TMS targets in left DLPFC (L-DLPFC) were calculated according to SNT algorithms (<xref ref-type="bibr" rid="B22">22</xref>&#x2013;<xref ref-type="bibr" rid="B24">24</xref>). Firstly, each patient&#x2019;s L-DLPFC and subgenual anterior cingulate cortex (sgACC) regions were subdivided into numerous functional subnuclei defined according to correlated voxel pairs using a hierarchical agglomerative clustering algorithm. For each subnucleus in L-DLPFC and sgACC, a single time-series value representing the single voxel time series that was most correlated with the median time series was identified. The correlation matrix between L-DLPFC and sgACC subnuclei was then calculated. Secondly, the optimal targets in L-DLPFC were determined by considering the most anticorrelation subnucleus, the larger size of subnucleus, and the higher spatial concentration, which are equally weighted in this algorithm.</p>
<p>IT-TMS was performed using the Black Dolphin Navigation Robot (S-50, a sub-millimeter smart positioning system, Solide Medical Co., Ltd., Xi&#x2019;an, Shaanxi, China) with a figure-of-8 coil (YINGCHI, Shenzhen, China) by trained professionals. A 3D-printed mask with ball-like tracking points was attached to the patient&#x2019;s head. The position of the tracking points and the location and orientation of the coil were co-registered and visualized by an infrared camera system, which allowed the precise and repetitive navigation of the coil over the target area under real-time visualization. Fifty intermittent theta-burst stimulation (iTBS) sessions (1,800 pulses per session, 50-min intervals) were delivered in 10 daily sessions over 5 consecutive days at a 90% resting motor threshold. These parameters were set according to SNT that was approved by FDA (<xref ref-type="bibr" rid="B25">25</xref>).</p>
</sec>
<sec id="s2_5">
<title>Clinical assessment</title>
<p>Suicidal ideation was assessed using the BSI-CV and HAMD-17 before (baseline) and after IT-TMS therapy (follow-up: immediately, 15 days and 30 days after the last treatment). The assessment was done by the same trained physiotherapist. Response of suicidal ideation was defined as the reduction of more than 50% relative to the baseline BSI-CV score, and remission was defined as that BSI-CV score was 0 (<xref ref-type="bibr" rid="B22">22</xref>). Response of depression was defined as the reduction of more than 50% relative to the baseline HAMD-17 score, and remission was defined as that HAMD-17 score was less than 7.</p>
</sec>
<sec id="s2_6">
<title>Brain network analysis</title>
<p>GRETNA software (<ext-link ext-link-type="uri" xlink:href="http://www.nitrc.org/projects/gretna">http://www.nitrc.org/projects/gretna</ext-link>) was used to analyze brain network characteristics according to graph theory (<xref ref-type="bibr" rid="B11">11</xref>). Briefly, the whole brain was divided into 116 network nodes based on the automated anatomical labeling (AAL) atlas. Pearson correlation coefficient between the time series of all possible pairs of nodes was calculated, yielding a 116 &#xd7; 116 correlation matrix for each subject, which was then transformed into an undirected binarized matrix using sparsity thresholding (5% &#x2264; s &#x2264; 40%) at an interval of 0.1. The functional segregation metrics consist of clustering coefficient (Cp), normalized clustering coefficient (&#x3b3;), and local efficiency (Eloc). The functional integration metrics consist of characteristic path length (Lp), normalized characteristic path length (&#x3bb;), and global efficiency (Eglob). The small-world metric includes &#x3c3; (&#x3c3; = &#x3b3;/&#x3bb;). These metrics were all obtained. The area under the curve (AUC) for each network metric was calculated for further statistical comparisons.</p>
</sec>
<sec id="s2_7">
<title>Statistical analysis</title>
<p>SPSS software (version 26) was used for statistical analysis. Differences in demographic information (HCs vs. patients at baseline) and clinical scales (HCs vs. patients at baseline) were compared using the chi-square test and Student&#x2019;s <italic>t</italic>-test. Differences in clinical scales (patients at baseline vs. patients at follow-up) were compared using ANOVA for repeated measurement. The demographic and clinical data were expressed as mean &#xb1; Standard Deviation (SD). Two-sample <italic>t</italic>-test (HCs vs. patients at baseline) or paired <italic>t</italic>-test (patients at baseline vs. patients at follow-up) were used to identify changes in global network metrics. The AUC values of each network metric showing abnormal differences were extracted and drawn. A network-based statistic (NBS) approach and paired <italic>t</italic>-test were used to reveal any significant differences in Edges and Nodes of node network (patients at baseline vs. patients at follow-up). BrainNet software was then used to visualize the brain regions with statistical differences. <italic>P</italic> value in node network was calculated using MedCalc software. Pearson analysis was performed to examine the correlation between changes in network metrics and clinical scores. Multiple comparisons were corrected by false discovery rate (FDR) with a corrected significance level of <italic>P</italic> = 0.05.</p>
</sec>
</sec>
<sec id="s3" sec-type="results">
<title>Results</title>
<sec id="s3_1">
<title>Subjects</title>
<p>A total of 36 patients (aged 18-55) and 28 HCs (aged 20-51) had been recruited, among which 4 patients were excluded. All patients had suicidal ideation at the time of screening for BSI-CV (score &gt; 6), and depression symptom for HAMD-17 (score &gt; 17). There was no significant difference in age (<italic>P</italic> = 0.358), gender (<italic>P</italic> = 0.365), and year of education (<italic>P</italic> = 0.061) between patients and HCs (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>). The patients had significantly higher BSI-CV (17.6 &#xb1; 7.06, <italic>P</italic> = 0.000) and HAMD-17 (27.9 &#xb1; 4.31, <italic>P</italic> = 0.000) scores compared with HCs (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>). All patients were tolerable to TMS without dropping out. None of the HCs had psychopathy currently or previously. Detailed information is listed in <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>. The STROBE flow diagram is shown below in <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Demographic and clinical characteristics of subjects at baseline.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="left">Characteristics (mean (SD))</th>
<th valign="middle" align="left">Patients (n=32)</th>
<th valign="middle" align="left">Healthy controls (n=28)</th>
<th valign="middle" align="left">
<italic>P</italic> value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">Age (years)</td>
<td valign="middle" align="left">27.7 (10.38)</td>
<td valign="middle" align="left">29.6 (5.01)</td>
<td valign="middle" align="left">0.358</td>
</tr>
<tr>
<td valign="middle" align="left">Gender (Male/Female)</td>
<td valign="middle" align="left">5/27</td>
<td valign="middle" align="left">7/21</td>
<td valign="middle" align="left">0.365</td>
</tr>
<tr>
<td valign="middle" align="left">Education (years)</td>
<td valign="middle" align="left">13.34 (2.79)</td>
<td valign="middle" align="left">15.8 (1.93)</td>
<td valign="middle" align="left">0.061</td>
</tr>
<tr>
<td valign="middle" align="left">BSI-CV</td>
<td valign="middle" align="left">17.6 (7.06)</td>
<td valign="middle" align="left">0.0 (0.00)</td>
<td valign="middle" align="left">&lt; 0.0001</td>
</tr>
<tr>
<td valign="middle" align="left">HAMD-17</td>
<td valign="middle" align="left">27.9 (4.31)</td>
<td valign="middle" align="left">4.4 (2.60)</td>
<td valign="middle" align="left">&lt; 0.0001</td>
</tr>
<tr>
<td valign="middle" align="left">Duration of illness (months)</td>
<td valign="middle" align="left">11.4 (1.39)</td>
<td valign="middle" align="left">&#x2013;</td>
<td valign="middle" align="left">&#x2013;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>At baseline, demographic and clinical characteristics were compared between patients and healthy controls.</p>
</fn>
<fn>
<p>P value: healthy controls vs. patients at baseline; SD, standard deviation; BSI-CV, Beck Scale for Suicide Ideation-Chinese Version; HAMD-17, 17-item Hamilton Depression Rating Scale.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>The STROBE flow diagram.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-16-1486835-g001.tif"/>
</fig>
<p>As shown in <xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref>, patients showed significant reduction in BSI-CV ((6.1 &#xb1; 5.98) &lt; 6, <italic>P</italic> &lt; 0.001) and HAMD-17 ((9.4 &#xb1; 5.43) &lt; 17, <italic>P</italic> &lt; 0.001) scores immediately after IT-TMS treatment. Moreover, the scores acquired 15 and 30 days after treatment continued the trend of decrease. The response and remission rates of suicidal ideation reached 93.75% and 37.50%, respectively, 30 days after treatment. There were no missing data in this study.</p>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Clinical characteristics of patients before and after IT-TMS.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" rowspan="3" align="left">Characteristics</th>
<th valign="top" rowspan="3" align="center">Baseline (n=32)</th>
<th valign="top" colspan="12" align="center">Follow-up (n=32)</th>
</tr>
<tr>
<th valign="middle" colspan="4" align="center">Immediately after IT-TMS treatment</th>
<th valign="middle" colspan="4" align="center">15 days after IT-TMS treatment</th>
<th valign="middle" colspan="4" align="center">30 days after IT-TMS treatment</th>
</tr>
<tr>
<th valign="middle" align="center">Mean (SD)</th>
<th valign="middle" align="center">
<italic>P</italic>
</th>
<th valign="middle" align="center">Response (%)</th>
<th valign="middle" align="center">Remission (%)</th>
<th valign="middle" align="center">Mean (SD)</th>
<th valign="middle" align="center">
<italic>P</italic>
</th>
<th valign="middle" align="center">Response (%)</th>
<th valign="middle" align="center">Remission (%)</th>
<th valign="middle" align="center">Mean (SD)</th>
<th valign="middle" align="center">
<italic>P</italic>
</th>
<th valign="middle" align="center">Response (%)</th>
<th valign="middle" align="center">Remission (%)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">BSI-CV</td>
<td valign="middle" align="center">17.6 (7.06)</td>
<td valign="top" align="center">6.1 (5.98)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">65.63</td>
<td valign="top" align="center">28.13</td>
<td valign="top" align="center">5.8 (6.01)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">75.00</td>
<td valign="top" align="center">28.13</td>
<td valign="top" align="center">3.2 (4.53)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">93.75</td>
<td valign="top" align="center">37.50</td>
</tr>
<tr>
<td valign="top" align="left">HAMD-17</td>
<td valign="middle" align="center">27.9 (4.31)</td>
<td valign="top" align="center">9.4 (5.43)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">84.38</td>
<td valign="top" align="center">31.25</td>
<td valign="top" align="center">7.8 (4.57)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">93.75</td>
<td valign="top" align="center">50.00</td>
<td valign="top" align="center">5.5 (4.24)</td>
<td valign="top" align="center">&lt; 0.0001</td>
<td valign="top" align="center">96.88</td>
<td valign="top" align="center">71.88</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>BSI-CV and HAMD-17 scores were compared before and after IT-TMS treatment.</p>
</fn>
<fn>
<p>P value: patients at baseline vs. patients at follow-up in BSI-CV or HAMD-17 scales; SD, standard deviation; IT-TMS, individual target-transcranial magnetic stimulation; BSI-CV, Beck Scale for Suicide Ideation-Chinese Version; HAMD-17, 17-item Hamilton Depression Rating Scale.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3_2">
<title>Global network</title>
<p>Overall, the functional networks of all three groups (HCs at baseline, patients at baseline and patients at follow-up) conformed to the small-world attribution (&#x3c3; &gt; 1, &#x3b3; &gt; 1, &#x3bb; &#x2248; 1, <xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>) using sparsity thresholding between 0.05 and 0.40. In addition, two-sample <italic>t</italic>-test results indicated that MDD/SI+ patients at baseline had altered global properties (decreased &#x3c3;), reduced functional segregation metrics (Cp and Eloc), and abnormal functional integration metrics (increased Lp and decreased Eglob) compared with HCs at baseline. After IT-TMS treatment in the patients&#x2019; group, the above metrics at follow-up were significantly reversed compared with baseline (paired <italic>t</italic>-test, <italic>P</italic> &lt; 0.05), indicating that the efficiency of functional separation and functional integration was improved.</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Alteration of global topological properties across the sparsity from 0.05 to 0.40, including the typical small-world network architectures (<bold>A</bold> &#x3c3; &gt; 1, <bold>B</bold>: &#x3b3; &gt; 1, and <bold>C</bold>: &#x3bb; &#x2248; 1), the functional segregation metrics (<bold>D</bold>: Eloc and <bold>E</bold>: Cp) and the functional integration metrics (<bold>F</bold>: Eglob and <bold>G</bold>: Lp). The solid circle stands for the healthy control, the cross for the MDD/SI+ patients at baseline and the hollow circle for patients at follow-up. The area under the curve (AUC) for each topological property in healthy control at baseline, patients at baseline and patients at follow-up was calculated. *<italic>P</italic>&lt;0.05. **<italic>P</italic>&lt;0.01.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-16-1486835-g002.tif"/>
</fig>
</sec>
<sec id="s3_3">
<title>Node network</title>
<p>After NBS multiple correction and paired <italic>t</italic>-test (<italic>P</italic> &lt; 0.05), the patients showed reduced functional connections of nodes at follow-up compared with baseline values. The nodes were mainly located at superior frontal gyrus, anterior cingulate gyrus (ACG), insula, amygdala, thalamus and middle frontal gyrus (orbital part) (<xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>). Detailed connections (Edges and Nodes) are shown in <xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>.</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Node network with altered functional connections.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Regions</th>
<th valign="top" align="left">Betweenness (<italic>P</italic>)</th>
<th valign="top" align="left">Centrality (<italic>P</italic>)</th>
<th valign="top" align="left">Nodal efficiency (<italic>P</italic>)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">baseline &gt; follow-up</td>
<td valign="top" align="left"/>
<td valign="top" align="left"/>
<td valign="top" align="left"/>
</tr>
<tr>
<th valign="top" colspan="4" align="left">Left</th>
</tr>
<tr>
<td valign="top" align="left">Superior frontal gyrus (dorsolateral) (SFGdor)</td>
<td valign="top" align="left">0.0045</td>
<td valign="top" align="left">0.0012</td>
<td valign="top" align="left">0.0029</td>
</tr>
<tr>
<td valign="top" align="left">Insula (INS)</td>
<td valign="top" align="left">0.1038</td>
<td valign="top" align="left">0.0139</td>
<td valign="top" align="left">0.0289</td>
</tr>
<tr>
<td valign="top" align="left">Anterior cingulate gyrus (ACG)</td>
<td valign="top" align="left">0.0027</td>
<td valign="top" align="left">0.0148</td>
<td valign="top" align="left">0.0401</td>
</tr>
<tr>
<td valign="top" align="left">Amygdala (AMYG)</td>
<td valign="top" align="left">0.0010</td>
<td valign="top" align="left">0.0318</td>
<td valign="top" align="left">0.0180</td>
</tr>
<tr>
<td valign="top" align="left">Thalamus (THA)</td>
<td valign="top" align="left">0.0015</td>
<td valign="top" align="left">0.1469</td>
<td valign="top" align="left">0.1388</td>
</tr>
<tr>
<th valign="top" colspan="4" align="left">Right</th>
</tr>
<tr>
<td valign="top" align="left">Precuneus (PCUN)</td>
<td valign="top" align="left">0.0008</td>
<td valign="top" align="left">0.0201</td>
<td valign="top" align="left">0.0378</td>
</tr>
<tr>
<td valign="top" align="left">Middle frontal gyrus (orbital part) (ORBmid)</td>
<td valign="top" align="left">0.0108</td>
<td valign="top" align="left">0.0358</td>
<td valign="top" align="left">0.1569</td>
</tr>
<tr>
<td valign="top" align="left">Insula (INS)</td>
<td valign="top" align="left">0.0098</td>
<td valign="top" align="left">0.0016</td>
<td valign="top" align="left">0.0018</td>
</tr>
<tr>
<td valign="top" align="left">Amygdala (AMYG)</td>
<td valign="top" align="left">0.0021</td>
<td valign="top" align="left">0.0250</td>
<td valign="top" align="left">0.0468</td>
</tr>
<tr>
<td valign="top" align="left">Thalamus (THA)</td>
<td valign="top" align="left">0.0016</td>
<td valign="top" align="left">0.0156</td>
<td valign="top" align="left">0.0038</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Alteration of functional connections of the node network after IT-TMS treatment in the patients. L, left; R, right. The nodes (blue points) and edges (yellow lines) are shown in this figure. The corresponding brain regions are also marked. The nodes were mainly located at superior frontal gyrus, anterior cingulate gyrus (ACG), insula, amygdala, thalamus and middle frontal gyrus (orbital part).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-16-1486835-g003.tif"/>
</fig>
</sec>
<sec id="s3_4">
<title>Correlation analysis</title>
<p>Although no significant correlations were found between the small-world properties and clinical characteristics, a significant positive correlation was found between improvements in BSI-CV (baseline score minus score acquired immediately after the last treatment) and changes in functional connectivity between right insula and left ACG (<italic>r</italic> = 0.57, <italic>p</italic> &lt; 0.001). The correlation result is shown in <xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>.</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>A significant positive correlation between improvements in BSI-CV and changes in functional connectivity between right insula and left ACG (<italic>r</italic> = 0.57, <italic>p</italic> &lt; 0.001). BSI-CV: Beck Scale for Suicide Ideation-Chinese Version. ACG, anterior cingulate gyrus. Follow-up: immediately after the last treatment.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-16-1486835-g004.tif"/>
</fig>
</sec>
</sec>
<sec id="s4" sec-type="discussion">
<title>Discussion</title>
<p>This study focused on the manifestation of cerebral topological structure in MDD/SI+ patients. Using MRI data based on graph-theory analysis, the functional network of all these three groups was found to conform to small-world topology. However, at baseline, MDD/SI+ patients exhibited impaired and inefficient small-world properties and aberrant functional segregation and functional integration compared with the HCs. These properties showed a renormalization after IT-TMS treatment. We found that patients after IT-TMS treatment targeting individualized DLPFC sites led to significant reduction in suicidal ideation and depressive symptom. The clinical scales in <xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref> demonstrated the downtrend of BSI-CV and HAMD-17 scores till the end of 30 days after treatment, which confirmed the lasting effects of IT-TMS. Some key nodes were discovered, including superior frontal gyrus, ACG, insula, amygdala, thalamus and middle frontal gyrus (orbital part). Furthermore, decreased functional connectivity between right insula and left ACG correlated with improvement in BSI-CV scores. The current study highlights that MDD/SI+ patients in this cohort showed abnormal brain network connections compared to healthy controls, and that TMS may exert its treatment effects by reducing spontaneous hyper-connectivity in the salience network and insula.</p>
<p>Venlafaxine and duloxetine have quick effects on depressive and suicidal behavior. Considering that patients might conduct suicidal behavior if medications were taken away, they took venlafaxine or duloxetine constantly during IT-TMS treatment, which also met the principles of ethical review and safety requirements. As a result, false-positive results and confounding effects may exist. The sham TMS group and medication-only group are being conducted to exclude false-positive results. In addition, Alina Zaidi et&#xa0;al. concluded that the combination of rTMS with antidepressants significantly reduced depression severity, increasing response and remission rates (<xref ref-type="bibr" rid="B26">26</xref>). In consequence, a conclusion that IT-TMS (concurrent medication) exerts better effects can be drawn, but to what extent IT-TMS may interact with medication remains to be explored.</p>
<p>Brain is a complex information system to coordinate multiple regions as a network, hence it is necessary to study the neural mechanisms of MDD/SI+ from a network perspective. Using graph theory-based analysis methods, MDD/SI+ patients demonstrated poorly efficient network properties (&#x3c3;), reduced functional segregation (Cp and Eloc) and abnormal functional integration metrics (Lp and Eglob) at baseline (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>), indicating that the balance between energy cost and communication efficiency had been broken. Functional segregation refers to local network efficiency, and reduced Cp and Eloc indicates that the &#x201c;speed&#x201d; of information transfer between adjacent nodes within a network is compromised (<xref ref-type="bibr" rid="B27">27</xref>). Functional integration ensures prompt interregional transfer of information, and abnormal functional integration (lower Eglob and higher Lp) indicates that the parallel information transfer in a brain network and communication efficiency are impaired (<xref ref-type="bibr" rid="B28">28</xref>). Consistent with these conclusions, this study indicates that MDD/SI+ in this cohort is a dysconnectivity disorder involving multiple neuronal circuits and brain networks, rather than a focal pathology affecting a single or certain regions. Moreover, the graph-theory metrics (Eloc, Cp, Eglob and Lp) were significantly restored after IT-TMS treatment, indicating that both local and global network efficiency were recovered. The rebuilding of information transfer within a network and recovering of interregional transfer of information ensured the rebalance between energy cost and communication efficiency. As a result, depressive symptoms and suicidal ideation were relieved. The previous studies showed that direction of flow of brain activity from left anterior insula to ACC was significantly reversed in MDD patients, hence ACC-based directed signaling patterns are a potential biomarker for MDD (<xref ref-type="bibr" rid="B29">29</xref>). This flow was abnormally from ACC to anterior insula, enlightening us to focus on these two brain regions. Under normal circumstances, the anterior insula is the region that belongs to salience network and integrates physical sensations and sends signals to ACC, the region that controls emotions to maintain normal mental state. Our study used TMS to significantly improve suicidal scales and relieve suicidal symptoms among MDD patients with extra suicidal ideation (<xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref>), and the insula-related functional connectivity was notably decreased (<xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>, <xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>), indicating that the ability of insula to block irrelevant information and prevent interference from sensory signals has improved. This was consistent with illustrations that improvement in MDD is strongly associated with functional recovery in the insula and anterior cingulate area. Additionally, the more improved BSI-CV scales showed, the less functional connectivity between right insula and left ACG (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>), suggesting that TMS relieved the interference with insula function. As a result, TMS exerted therapeutic effects by reducing the connectivity between right insula and left ACG, which may be potential imaging markers for the diagnosis and treatment of MDD/SI+.</p>
</sec>
<sec id="s5">
<title>Limitations and conclusion</title>
<p>To our knowledge, this study is the first to examine graph-theory network alterations after TMS therapy for MDD/SI+ patients. In conclusion, our study concluded that MDD/SI+ was a dysfunction of multiple brain networks, rather than a focal pathology affecting a single or certain regions. IT-TMS exerted better therapeutic effects by reducing the connectivity between right insula and left ACG, which may ultimately inform a clinical protocol for the remission of suicidal ideation and depressive symptoms.</p>
<p>This study has several limitations. Firstly, the sample size is relatively small, which is limited by the number of enrolled subjects, because this is single-center research. This may not reflect the overall characteristics of MDD/SI+ patients. Secondly, the long-lasting (not limited to 30 days) effects of IT-TMS still need to be verified. Finally, the graph-theory results need to be further explained to verify the relationship between MDD/SI+ and network alterations.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="data-availability">
<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="s7" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The studies involving humans were approved by the Research Ethics Review Board of the Institute of Mental Health of Xijing Hospital. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="s8" sec-type="author-contributions">
<title>Author contributions</title>
<p>YZ: Conceptualization, Formal analysis, Investigation, Methodology, Resources, Validation, Writing &#x2013; original draft. NM: Conceptualization, Formal analysis, Investigation, Methodology, Resources, Validation, Writing &#x2013; original draft. SQ: Formal analysis, Investigation, Validation, Writing &#x2013; review &amp; editing. CS: Formal analysis, Methodology, Software, Validation, Writing &#x2013; original draft. YR: Formal analysis, Methodology, Validation, Writing &#x2013; review &amp; editing. XY: Formal analysis, Validation, Writing &#x2013; original draft. JG: Data curation, Formal analysis, Resources, Software, Writing &#x2013; original draft. YM: Data curation, Formal analysis, Project administration, Resources, Writing &#x2013; review &amp; editing.</p>
</sec>
<sec id="s9" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article.This work was supported by fast response research topic of Air Force Medical University (No. 2023KXKT048), National Natural Science Foundation of China (No. 82371529 and 82330043) and Shaanxi Province technology innovation guidance program project (No. 2024QCY-KXJ-035).</p>
</sec>
<ack>
<title>Acknowledgments</title>
<p>We want to give special thanks to Shaanxi Brain Modulation and Scientific Research Center, for its kind help and cooperation. All subjects have been thanked for their contributions, including language editing.</p>
</ack>
<sec id="s10" sec-type="COI-statement">
<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 id="s11" 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>
<fn-group>
<title>Abbreviations</title>
<fn fn-type="abbr" id="abbrev1">
<p>MDD/SI+, Major depressive disorder with suicidal ideation; IT-TMS, Individual target-transcranial magnetic stimulation; DLPFC, dorsolateral prefrontal cortex; L-DLPFC: left dorsolateral prefrontal cortex; MDD/SB+, Major depressive disorder with suicide behavior; SNT, Stanford Neuromodulation Therapy; HAMD-17, 17-item Hamilton Depression Rating Scale score; BSI-CV, Beck Scale for Suicide Ideation-Chinese Version; HCs, Healthy controls; sgACC, subgenual anterior cingulate cortex; iTBS, intermittent theta-burst stimulation.</p>
</fn>
</fn-group>
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