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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Oncol.</journal-id>
<journal-title>Frontiers in Oncology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Oncol.</abbrev-journal-title>
<issn pub-type="epub">2234-943X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fonc.2025.1626529</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Oncology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The risk prediction model for acute urine retention after perineal prostate biopsy based on the LASSO approach and Boruta feature selection</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Shen</surname>
<given-names>Cheng</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1987344/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Chen</surname>
<given-names>Gen</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Chen</surname>
<given-names>Zhan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/998299/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>You</surname>
<given-names>Junjie</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/project-administration/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Zheng</surname>
<given-names>Bing</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1397439/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
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</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Urology, Affiliated Hospital 2 of Nantong University</institution>, <addr-line>Nantong, Jiangsu</addr-line>,&#xa0;<country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Jiangsu Nantong Urological Clinical Medical Center</institution>, <addr-line>Nantong, Jiangsu</addr-line>,&#xa0;<country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Institute of Urological Diseases, Nantong University</institution>, <addr-line>Nantong, Jiangsu</addr-line>,&#xa0;<country>China</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Urology, Nantong Second People&#x2019;s Hospital</institution>, <addr-line>Nantong, Jiangsu</addr-line>,&#xa0;<country>China</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Department of Urology, Rudong Hospital, Xinglin College of Nantong University</institution>, <addr-line>Nantong, Jiangsu</addr-line>,&#xa0;<country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1684905/overview">Wenlin Yang</ext-link>, University of Florida, United States</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2144297/overview">Shuai Chen</ext-link>, Affiliated Hospital of Jining Medical University, China</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3172912/overview">Manikandan Ganesan</ext-link>, SASTRA University, India</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Junjie You, <email xlink:href="mailto:972482570@qq.com">972482570@qq.com</email>; Bing Zheng, <email xlink:href="mailto:ntzb2008@163.com">ntzb2008@163.com</email>
</p>
</fn>
<fn fn-type="equal" id="fn003">
<p>&#x2020;These authors have contributed equally to this work</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>11</day>
<month>09</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>15</volume>
<elocation-id>1626529</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>05</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>29</day>
<month>08</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Shen, Chen, Chen, You and Zheng.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Shen, Chen, Chen, You and Zheng</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>Objective</title>
<p>One known side effect of transperineal (TP) prostate biopsies is acute urine retention (AUR). We aimed to create and evaluate a predictive model for the post-paracentesis risk of acquiring AUR.</p>
</sec>
<sec>
<title>Methods</title>
<p>This study included 599 patients undergoing prostate biopsies (April 2020-July 2023) at the Second Affiliated Hospital of Nantong University, selected based on abnormal digital rectal examination and/or PSA (prostate-specificantigen) &gt; 4 ng/mL. Acute urinary retention (AUR) was defined as the inability to void within 72 hours post-biopsy, requiring catheterization. Patients were randomly divided into training (419 cases) and test (180 cases) sets. Univariate logistic analysis and feature selection Boruta and LASSO (Least absolute shrinkage and selection operator) identified predictors, followed by multivariate logistic regression to develop a predictive nomogram for AUR. Internal validation used the test set, with model performance assessed via the c-index, ROC (Receiver Operating Characteristic) curve, calibration plot, and decision curve analysis. The nomogram demonstrated strong discrimination, calibration, and clinical utility for AUR risk prediction.</p>
</sec>
<sec>
<title>Results</title>
<p>In 86 patients (14.3%), AUR happened. An examination of multivariate logistic regression revealed six distinct risk variables for AUR. Based on these independent risk factors, a nomogram was constructed. The training and validation groups&#x2019; c-indices showed the model&#x2019;s high accuracy and stability. The calibration curve demonstrates that the corrective effect of the training and verification groups is perfect, and the area under the receiver operating characteristic curve indicates great identification capacity. DCA (Decision Curve Analysis) curves, or decision curve analysis, demonstrated the model&#x2019;s significant net therapeutic effect.</p>
</sec>
<sec>
<title>Discussion</title>
<p>The nomogram model created in this work can offer a personalized and intuitive analysis of the risk of AUR and has intense discrimination and accuracy. It can help create efficient preventative measures and identify high-risk populations.</p>
</sec>
</abstract>
<kwd-group>
<kwd>acute urinary retention</kwd>
<kwd>prostate biopsy</kwd>
<kwd>machine learning</kwd>
<kwd>predictive model</kwd>
<kwd>Boruta feature selection</kwd>
</kwd-group>
<counts>
<fig-count count="8"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="46"/>
<page-count count="12"/>
<word-count count="5218"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Genitourinary Oncology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<title>Introduction</title>
<p>In 2022, prostate cancer accounted for around 27% of all new cancer diagnoses in the United States and was the most common cancer diagnosis among men (<xref ref-type="bibr" rid="B1">1</xref>). Research has focused on prostate biopsies as the gold standard for diagnosing prostate cancer in recent years. There are two methods for prostate biopsies: transrectal (TR) and transperineal (TP) (<xref ref-type="bibr" rid="B2">2</xref>). TR has historically carried out prostate biopsies. The burden that postoperative sepsis places on patient health and adds to the expenditures to the healthcare system, however, is the primary critique of this strategy (<xref ref-type="bibr" rid="B3">3</xref>&#x2013;<xref ref-type="bibr" rid="B6">6</xref>). As a result of the declining percentage of TP biopsy in sepsis cases, there has been a nationwide movement to offer TP biopsy. AUR, or acute urinary retention, is another danger associated with prostate biopsies that may be higher than other TR techniques (<xref ref-type="bibr" rid="B7">7</xref>&#x2013;<xref ref-type="bibr" rid="B10">10</xref>). AUR frequently necessitates catheterization and additional hospitalization (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B12">12</xref>). While TP biopsy may lessen infection, it does not entirely prevent infection. According to studies referenced by NICE, urinary retention rates range from 1.6 to 11.4% (<xref ref-type="bibr" rid="B12">12</xref>).</p>
<p>Data evaluating possible risk factors for AUR after prostate biopsy in TP are currently hard to come by (<xref ref-type="bibr" rid="B13">13</xref>&#x2013;<xref ref-type="bibr" rid="B15">15</xref>). Because medical big data is so common, machine learning (ML), the most significant artificial intelligence implementation technique, has been applied extensively to data-driven risk prediction (<xref ref-type="bibr" rid="B16">16</xref>, <xref ref-type="bibr" rid="B17">17</xref>). Given the high dimensionality of the data, we chose to use LASSO first for preliminary screening to reduce Boruta &#x2018;s computational burden and improve the efficiency of the overall analysis. Therefore, after screening out risk factors using LASSO regression. We further screened variables using Boruta &#x2018;s feature screening method. We then iteratively processed random fluctuations in forest importance scores and factor interactions to screen for significant urinary retention predictors. In addition, this approach is commonly used for feature selection in diabetes mellitus (DM) studies (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>). In addition, Meng Zirui et&#xa0;al. constructed predictive models for severe novel coronavirus pneumonia using variant analysis and least absolute contraction and selection operator (LASSO) modeling along with Boruta &#x2018;s algorithm (<xref ref-type="bibr" rid="B20">20</xref>). Ding Xuexuan et&#xa0;al. identified the core genes of asthma using five machine learning algorithms: LASSO, SVM-RFE, Boruta, XGBoost, and RF (<xref ref-type="bibr" rid="B21">21</xref>).</p>
<p>In view of the high clinical incidence of acute urinary retention (AUR) after transperineal prostate puncture (TP) and the lack of a precise predictive model for this complication, the aim of this study was to construct and validate a nomogram model that can be used to rapidly assess the risk of AUR preoperatively by integrating clinical routine indicators (such as BMI, prostate volume, etc.) using LASSO and Boruta feature selection algorithms to provide a quantitative tool for clinical decision-making in order to reduce the postoperative catheter indwelling rate and length of hospital stay.</p>
</sec>
<sec id="s2">
<title>Patients and methods</title>
<sec id="s2_1">
<title>Study design and participants</title>
<p>We conducted a retrospective analysis of a cohort of patients who underwent prostate biopsy in the day ward of the Department of Urology, the First People&#x2019;s Hospital of Nantong, from April 2020 to July 2023. Abnormal digital rectal examination, high PSA (&gt; 4.0 ng/mL), or positive prostate multiparametric MRI (prostate imaging report and data system &#x2265; 3) were the inclusion criteria. The following conditions precluded study participation: hypersensitivity to ciprofloxacin, prostate-related surgery within the previous three months, urinary tract infection during biopsy or therapy, and denial of informed written consent. The study excluded patients with a history of urine retention and those with urinary retention during biopsy. Data parameters included patient demographics, PSA readings, the International Prostate Symptom Score (IPSS), prostate volume, post-void residual (PVR) volume before biopsy, comorbidities, blood and urine routines, post-void residual (PVR) volume, and histopathological findings.</p>
</sec>
<sec id="s2_2">
<title>Ethics and informed consent</title>
<p>The research adhered to the principles outlined in the Declaration of Helsinki. All subjects gave informed consent, which was approved by the First People&#x2019;s Hospital Center of Nantong&#x2019;s Ethics Committee (ethical approval number 2022KT100). Because this study was a retrospective cross-sectional study, informed consent was not required and all subjects included in the study had signed an informed consent form authorizing the use of the information for future scientific research. Retrospective data analysis followed the ethical guidelines applicable at the time of source data collection (Declaration of Helsinki 2013 revision).</p>
</sec>
<sec id="s2_3">
<title>Data collection and variable definition</title>
<p>Demographic information was obtained from electronic medical records, along with PSA values, the International Prostate Symptom Score (IPSS), prostate volume, post-void residual (PVR) volume before biopsy, comorbidities, blood and urine routines, routine inflammatory parameters, and post-void residual (PVR) volume. Before being included in the study, a second reviewer verified the chart review data&#x2019;s accuracy. We used multiple imputation to handle missing values, the number of imputations was 5, and variables with &lt; 5% missing proportion were finally retained; abnormal values (identified by Z-score method, | Z | &gt; 3) were verified, corrected after confirming abnormal values due to measurement error, and the rest retained original data to avoid information loss; normality tests were performed for continuous variables (e.g., prostate volume, IPSS score), and logarithmic transformation was used for non-normally distributed variables (e.g., residual urine volume) to ensure the rationality of model input data. AUR was defined as the inability to void within 72 hours following biopsy, necessitating the implantation of a urinary catheter (<xref ref-type="bibr" rid="B22">22</xref>).</p>
</sec>
<sec id="s2_4">
<title>Histopathologic evaluation</title>
<p>All biopsies were analyzed by 2 urogenital pathologists (&gt; 10 years&#x2019; experience). The location, proportion of cancer tissue per core, and Gleason score (GS), based on the 2005 consensus of the International Society of Uropathology (<xref ref-type="bibr" rid="B23">23</xref>), were recorded for each prostate cancer-positive biopsy core.</p>
</sec>
<sec id="s2_5">
<title>PI-RADS score</title>
<p>Before having a prostate biopsy, all patients had 3.0 T mpMRIs (no endorectal coils). T1-weighted imaging (T1WI), T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and dynamic contrast-enhanced imaging (DCE) are among the scanning techniques used for mpMRI. After DWI data were collected at b-values of 0 and 1500 s/mm 2, ADC maps were produced. Two genitourinary radiologists with at least three years of prostate MRI expertise evaluated the mpMRI, and the PI-RADSv2.1 score was used to record the results. For CSPCa, it is doubtful to originate in PI-RADS 1 (doubtful to occur in CSPCa), PI-RADS 2 (unlikely to happen in CSPCa), and PI-RADS 3 (suspicious for CSPCa); nevertheless, for PI-RADS 4 (high) and PI-RADS 5 (very high) (<xref ref-type="bibr" rid="B24">24</xref>, <xref ref-type="bibr" rid="B25">25</xref>).</p>
</sec>
<sec id="s2_6">
<title>Statistical analysis</title>
<p>The continuous data were evaluated using the Student&#x2019;s t-test or the Mann-Whitney U test, and the results were reported as mean &#xb1; standard deviation (SD) or median and interquartile range. Alternatively, categorical data reported as numbers (%) was evaluated using Fisher&#x2019;s exact or Chi-square tests. We used LASSO regression to reduce the dimension of high-dimensional data and identify the best predictive characteristics and variables of AUR after performing univariate logistic regression analysis of the training group to first screen the factors and determine the risk factors of AUR (<xref ref-type="bibr" rid="B26">26</xref>). In addition, we employed Boruta&#x2019;s technique for feature selection, which involved 100 random forest iterations and the creation of logistic regression prediction models. Nomograms are validated by measuring their calibration (calibration graph) and discriminant capacity (C-statistic). C-statistic values above 0.75 are generally indicative of comparatively excellent discriminant ability. Lastly, we used decision curve analysis (DCA) to assess how applicable nomograms are in clinical practice. In every analysis, a p-value of less than 0.05 was deemed statistically significant.</p>
</sec>
</sec>
<sec id="s3" sec-type="results">
<title>Results</title>
<sec id="s3_1">
<title>Clinical features</title>
<p>Between January 1, 2020, and December 31, 2023, 599 patients who underwent prostate biopsies in Urology Department Day Ward at the Second Affiliated Hospital of Nantong University provided data for our analysis. Of these, 513 cases (85.64%) did not experience postoperative acute urine retention, while 86 (14.36%) experienced it. <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref> is a flow chart of the case selection and study process. The patients&#x2019; demographic features are detailed in <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>.</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Research pathway diagram.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g001.tif">
<alt-text content-type="machine-generated">Flowchart detailing a study on prostate biopsy. It starts with 622 patients, excludes 23 for various reasons, leaving 599. Data split into training (419) and validation (180) cohorts. Univariate and Lasso regression, Boruta feature selection, and logistic multivariate regression analysis are conducted. A nomogram model is constructed and verified for discrimination, calibration, clinical utility, and rationality.</alt-text>
</graphic>
</fig>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Baseline characteristics of patients.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="center">Characteristics</th>
<th valign="middle" align="center">Total (N=599)</th>
<th valign="middle" align="center">No AUR (N=513)</th>
<th valign="middle" align="center">AUR (N=86)</th>
<th valign="middle" align="center">P</th>
<th valign="middle" align="center">Statistic</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="center">Age(year)</td>
<td valign="middle" align="center">72.00[67.00;77.00]</td>
<td valign="middle" align="center">72.00 [67.00;77.00]</td>
<td valign="middle" align="center">73.00 [68.00;76.00]</td>
<td valign="middle" align="center">0.837</td>
<td valign="middle" align="center">21753</td>
</tr>
<tr>
<td valign="middle" align="center">BMI(kg/m^2)</td>
<td valign="middle" align="center">23.63[21.33;24.80]</td>
<td valign="middle" align="center">23.41 [21.19;24.74]</td>
<td valign="middle" align="center">24.59 [23.54;26.35]</td>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" align="center">13189.5</td>
</tr>
<tr>
<td valign="middle" align="center">Serum PSA(ng/ml)</td>
<td valign="middle" align="center">13.34 [7.56;23.73]</td>
<td valign="middle" align="center">13.34 [7.56;23.73]</td>
<td valign="middle" align="center">16.50 [11.24;22.69]</td>
<td valign="middle" align="center">0.018</td>
<td valign="middle" align="center">18536</td>
</tr>
<tr>
<td valign="middle" align="center">Prostate volume(ml)</td>
<td valign="middle" align="center">40.77[28.66;57.42]</td>
<td valign="middle" align="center">37.62 [27.95;49.76]</td>
<td valign="middle" align="center">98.17 [59.71;125.70]</td>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" align="center">6894</td>
</tr>
<tr>
<td valign="middle" align="center">Urine leukocyte</td>
<td valign="middle" align="center">17.00 [9.00;24.00]</td>
<td valign="middle" align="center">17.00 [9.00;24.00]</td>
<td valign="middle" align="center">17.00 [11.00;22.00]</td>
<td valign="middle" align="center">0.552</td>
<td valign="middle" align="center">22942</td>
</tr>
<tr>
<td valign="middle" align="center">Blood White cell</td>
<td valign="middle" align="center">6.90 [5.50;7.80]]</td>
<td valign="middle" align="center">6.90 [5.50;7.80]</td>
<td valign="middle" align="center">7.15 [5.82;7.77]</td>
<td valign="middle" align="center">0.979</td>
<td valign="middle" align="center">22020.5</td>
</tr>
<tr>
<td valign="middle" align="center">History of Electrocision</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.161</td>
<td valign="middle" rowspan="3" align="center">1.966</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">494 (82.47%)</td>
<td valign="middle" align="center">418 (81.48%)</td>
<td valign="middle" align="center">76 (88.37%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">105 (17.53%)</td>
<td valign="middle" align="center">95 (18.52%)</td>
<td valign="middle" align="center">10 (11.63%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Diabetes</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" rowspan="3" align="center">54.496</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">405 (67.61%)</td>
<td valign="middle" align="center">377 (73.49%)</td>
<td valign="middle" align="center">28 (32.56%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">194 (32.39%)</td>
<td valign="middle" align="center">136 (26.51%)</td>
<td valign="middle" align="center">58 (67.44%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Constipation</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" rowspan="3" align="center">53.505</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">398 (66.44%)</td>
<td valign="middle" align="center">371 (72.32%)</td>
<td valign="middle" align="center">27 (31.40%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">201 (33.56%)</td>
<td valign="middle" align="center">142 (27.68%)</td>
<td valign="middle" align="center">59 (68.60%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Before biopsy PVR(ml)</td>
<td valign="middle" align="center">63.00 [42.00;89.00]</td>
<td valign="middle" align="center">56.00 [42.00;78.00]</td>
<td valign="middle" align="center">114.00 [88.00;156.00]</td>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" align="center">7272</td>
</tr>
<tr>
<td valign="middle" align="center">IPSS</td>
<td valign="middle" align="center">12.00 [8.00;19.00]</td>
<td valign="middle" align="center">12.00 [7.00;17.00]</td>
<td valign="middle" align="center">22.00 [12.00;28.00]</td>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" align="center">11758</td>
</tr>
<tr>
<td valign="middle" align="center">Repeated biopsies</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">6</td>
<td valign="middle" align="center">0.006</td>
<td valign="middle" rowspan="3" align="center">7.536</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">519 (86.64%)</td>
<td valign="middle" align="center">453 (88.30%)</td>
<td valign="middle" align="center">66 (76.74%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">80 (13.36%)</td>
<td valign="middle" align="center">60 (11.70%)</td>
<td valign="middle" align="center">20 (23.26%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">PI-RADS Score</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.623</td>
<td valign="middle" rowspan="4" align="center">0.946</td>
</tr>
<tr>
<td valign="middle" align="center">3</td>
<td valign="middle" align="center">184 (30.72%)</td>
<td valign="middle" align="center">159 (30.99%)</td>
<td valign="middle" align="center">25 (29.07%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">4</td>
<td valign="middle" align="center">223 (37.23%)</td>
<td valign="middle" align="center">187 (36.45%)</td>
<td valign="middle" align="center">36 (41.86%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">5</td>
<td valign="middle" align="center">192 (32.05%)</td>
<td valign="middle" align="center">167 (32.55%)</td>
<td valign="middle" align="center">25 (29.07%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Target Location</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" rowspan="3" align="center">17.394</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">316 (52.75%)</td>
<td valign="middle" align="center">289 (56.34%)</td>
<td valign="middle" align="center">27 (31.40%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">283 (47.25%)</td>
<td valign="middle" align="center">224 (43.66%)</td>
<td valign="middle" align="center">59 (68.60%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Number of needles</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.837</td>
<td valign="middle" rowspan="3" align="center">0.042</td>
</tr>
<tr>
<td valign="middle" align="center">12</td>
<td valign="middle" align="center">76 (12.69%)</td>
<td valign="middle" align="center">64 (12.48%)</td>
<td valign="middle" align="center">12 (13.95%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">16</td>
<td valign="middle" align="center">523 (87.31%)</td>
<td valign="middle" align="center">449 (87.52%)</td>
<td valign="middle" align="center">74 (86.05%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Prostate Ca</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.901</td>
<td valign="middle" rowspan="3" align="center">0.015</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">216 (36.06%)</td>
<td valign="middle" align="center">186 (36.26%)</td>
<td valign="middle" align="center">30 (34.88%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">383 (63.94%)</td>
<td valign="middle" align="center">327 (63.74%)</td>
<td valign="middle" align="center">56 (65.12%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Histopathologic inflammation</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">&lt;0.001</td>
<td valign="middle" rowspan="3" align="center">24.85</td>
</tr>
<tr>
<td valign="middle" align="center">NO</td>
<td valign="middle" align="center">413 (68.95%)</td>
<td valign="middle" align="center">374 (72.90%)</td>
<td valign="middle" align="center">39 (45.35%)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="center">Yes</td>
<td valign="middle" align="center">186 (31.05%)</td>
<td valign="middle" align="center">139 (27.10%)</td>
<td valign="middle" align="center">47 (54.65%)</td>
<td valign="middle" align="center"/>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>PSA, prostate-specific antigen; AUR, Acute urinary retention; IPSS, International Prostate Symptom Score.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3_2">
<title>Risk factors associated with AUR</title>
<p>For each univariate logistic regression analysis, we created a forest plot (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>). We created a forest plot for each univariate logistic regression analysis (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>). We employed LASSO regression to select variables and simplify the model due to the many covariates. We utilized a 10-fold cross-validation strategy for internal validation using Lambda as the dependent variable and pi incidence as the dependent variable. The choice for the &#x3bb; filter variable was Min. The Lasso method&#x2019;s numerical variable screening procedure, which uses 14 variable coefficients that fluctuate with penalty coefficients, is shown in <xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3A</bold>
</xref>. The initial integration factor&#x2019;s coefficient is compressed and eliminated from the model when the coefficient is 0. Every row represents a different variable. The target covariates were ascertained by applying 10-fold cross-validation and the area under the ROC curve (ACU), as illustrated in <xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3B</bold>
</xref>. Two lines represent Lambda. Min and Lambda. Lse and each red dot represent the confidence interval for the appropriate &#x3bb; value for the covariate of interest. We then used the Boruta feature selection algorithm on optimal parameters to help separate AUR patients from non-AUR patients. Six variables were ultimately chosen, including body mass index, prostate volume, history of diabetes, constipation, IPSS, and residual urine before biopsy (<xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3C</bold>
</xref>). After that, we divided the six variables into groups and used logistic multivariate regression to examine them. The outcomes of the univariate and multivariate logistic regression analyses are shown in <xref ref-type="table" rid="T2">
<bold>Tables&#xa0;2</bold>
</xref> and <xref ref-type="table" rid="T3">
<bold>3</bold>
</xref>, respectively.</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>A forest plot illustrating the all of characteristics identified by univariate logistic regression analyses.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g002.tif">
<alt-text content-type="machine-generated">Forest plot showing odds ratios (OR) with 95% confidence intervals for various prostate-related variables. Significant factors include histopathologic inflammation (OR 2.676), target location (OR 2.56), repeated biopsies (OR 2.318), IPSS (OR 1.131), and constipation (OR 6.504). P-values indicate statistical significance, particularly for inflammation, location, IPSS, and constipation. Arrows indicate wide confidence intervals for constipation and diabetes.</alt-text>
</graphic>
</fig>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Boruta algorithm is used for feature selection, while LASSO is used for significant variable selection. <bold>(A)</bold> The clinical features&#x2019; LASSO coefficient profiles. <bold>(B)</bold> Tenfold cross-validation in LASSO produced the ideal penalization coefficient lambda. The figure displays the minimal mean square error&#x2019;s lambda value. The most minor absolute shrinkage and selection operator is known as LASSO. <bold>(C)</bold> Boruta&#x2019;s choice of function. We could counteract the predictive capacity of variables through these randomization features by using blue controls, which were risk permutation characteristics. Green features were validated as applicable; red features did not help predict AUR. The y-axis, linked to the standard deviation derived from 100 iterations, shows the variation in accuracy between each Z-score on the feature and the control. Level thresholds represent significant differences in thresholds between features and controls.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g003.tif">
<alt-text content-type="machine-generated">Graph A shows coefficient paths against log lambda for multiple variables. Graph B displays mean squared error versus log lambda, with highlighted values. Graph C is a box plot comparing importance scores of various attributes, ranked from &#x201c;alkalin&#x201d; to &#x201c;Prostate volumedel&#x201d;.</alt-text>
</graphic>
</fig>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Univariate Cox regression analysis of risk factors associated with AUR in patients undergoing TP.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="center">Characteristics</th>
<th valign="middle" align="center">B</th>
<th valign="middle" align="center">SE</th>
<th valign="middle" align="center">OR</th>
<th valign="middle" align="center">CI</th>
<th valign="middle" align="center">Z</th>
<th valign="middle" align="center">P</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">Age(year)</td>
<td valign="middle" align="right">-0.013</td>
<td valign="middle" align="right">0.01827</td>
<td valign="middle" align="right">0.987</td>
<td valign="middle" align="left">0.987(0.952-1.023)</td>
<td valign="middle" align="right">-0.721</td>
<td valign="middle" align="right">0.471</td>
</tr>
<tr>
<td valign="middle" align="left">BMI(kg/m^2)</td>
<td valign="middle" align="right">0.262</td>
<td valign="middle" align="right">0.06779</td>
<td valign="middle" align="right">1.299</td>
<td valign="middle" align="left">1.299(1.141-1.49)</td>
<td valign="middle" align="right">3.858</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">Serum PSA(ng.ml)</td>
<td valign="middle" align="right">0.004</td>
<td valign="middle" align="right">0.00759</td>
<td valign="middle" align="right">1.004</td>
<td valign="middle" align="left">1.004(0.988-1.018)</td>
<td valign="middle" align="right">0.494</td>
<td valign="middle" align="right">0.621</td>
</tr>
<tr>
<td valign="middle" align="left">Prostate volume(ml)</td>
<td valign="middle" align="right">0.045</td>
<td valign="middle" align="right">0.00583</td>
<td valign="middle" align="right">1.046</td>
<td valign="middle" align="left">1.046(1.035-1.059)</td>
<td valign="middle" align="right">7.73</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">Urine leukocyte</td>
<td valign="middle" align="right">-0.009</td>
<td valign="middle" align="right">0.01302</td>
<td valign="middle" align="right">0.991</td>
<td valign="middle" align="left">0.991(0.965-1.016)</td>
<td valign="middle" align="right">-0.68</td>
<td valign="middle" align="right">0.497</td>
</tr>
<tr>
<td valign="middle" align="left">Blood white cell</td>
<td valign="middle" align="right">-0.01</td>
<td valign="middle" align="right">0.0984</td>
<td valign="middle" align="right">0.99</td>
<td valign="middle" align="left">0.99(0.816-1.201)</td>
<td valign="middle" align="right">-0.102</td>
<td valign="middle" align="right">0.919</td>
</tr>
<tr>
<td valign="middle" align="left">History of electrocision</td>
<td valign="middle" align="right">-0.991</td>
<td valign="middle" align="right">0.53748</td>
<td valign="middle" align="right">0.371</td>
<td valign="middle" align="left">0.371(0.109-0.95)</td>
<td valign="middle" align="right">-1.845</td>
<td valign="middle" align="right">0.065</td>
</tr>
<tr>
<td valign="middle" align="left">Diabetes</td>
<td valign="middle" align="right">1.644</td>
<td valign="middle" align="right">0.31042</td>
<td valign="middle" align="right">5.178</td>
<td valign="middle" align="left">5.178(2.847-9.673)</td>
<td valign="middle" align="right">5.298</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">constipation</td>
<td valign="middle" align="right">1.872</td>
<td valign="middle" align="right">0.32194</td>
<td valign="middle" align="right">6.504</td>
<td valign="middle" align="left">6.504(3.519-12.52)</td>
<td valign="middle" align="right">5.816</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">Before biopsy PVR(ml)</td>
<td valign="middle" align="right">0.035</td>
<td valign="middle" align="right">0.00464</td>
<td valign="middle" align="right">1.036</td>
<td valign="middle" align="left">1.036(1.027-1.046)</td>
<td valign="middle" align="right">7.591</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">IPSS</td>
<td valign="middle" align="right">0.123</td>
<td valign="middle" align="right">0.01993</td>
<td valign="middle" align="right">1.131</td>
<td valign="middle" align="left">1.131(1.089-1.178)</td>
<td valign="middle" align="right">6.185</td>
<td valign="middle" align="right">0</td>
</tr>
<tr>
<td valign="middle" align="left">Repeated biopsies</td>
<td valign="middle" align="right">0.841</td>
<td valign="middle" align="right">0.35673</td>
<td valign="middle" align="right">2.318</td>
<td valign="middle" align="left">2.318(1.119-4.574)</td>
<td valign="middle" align="right">2.357</td>
<td valign="middle" align="right">0.018</td>
</tr>
<tr>
<td valign="middle" align="left">PI-RADS Score 4</td>
<td valign="middle" align="right">0.182</td>
<td valign="middle" align="right">0.3591</td>
<td valign="middle" align="right">1.2</td>
<td valign="middle" align="left">1.2(0.598-2.467)</td>
<td valign="middle" align="right">0.508</td>
<td valign="middle" align="right">0.612</td>
</tr>
<tr>
<td valign="middle" align="left">PI-RADS Score 5</td>
<td valign="middle" align="right">-0.09</td>
<td valign="middle" align="right">0.38257</td>
<td valign="middle" align="right">0.914</td>
<td valign="middle" align="left">0.914(0.43-1.952)</td>
<td valign="middle" align="right">-0.234</td>
<td valign="middle" align="right">0.815</td>
</tr>
<tr>
<td valign="middle" align="left">Target Location</td>
<td valign="middle" align="right">0.94</td>
<td valign="middle" align="right">0.30865</td>
<td valign="middle" align="right">2.56</td>
<td valign="middle" align="left">2.56(1.415-4.777)</td>
<td valign="middle" align="right">3.045</td>
<td valign="middle" align="right">0.002</td>
</tr>
<tr>
<td valign="middle" align="left">Number of needles</td>
<td valign="middle" align="right">0.282</td>
<td valign="middle" align="right">0.45824</td>
<td valign="middle" align="right">1.326</td>
<td valign="middle" align="left">1.326(0.579-3.597)</td>
<td valign="middle" align="right">0.616</td>
<td valign="middle" align="right">0.538</td>
</tr>
<tr>
<td valign="middle" align="left">Prostate Ca</td>
<td valign="middle" align="right">0.289</td>
<td valign="middle" align="right">0.31827</td>
<td valign="middle" align="right">1.336</td>
<td valign="middle" align="left">1.336(0.727-2.553)</td>
<td valign="middle" align="right">0.909</td>
<td valign="middle" align="right">0.363</td>
</tr>
<tr>
<td valign="middle" align="left">Histopathologic inflammation</td>
<td valign="middle" align="right">0.984</td>
<td valign="middle" align="right">0.29808</td>
<td valign="middle" align="right">2.676</td>
<td valign="middle" align="left">2.676(1.492-4.825)</td>
<td valign="middle" align="right">3.302</td>
<td valign="middle" align="right">0.001</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>AUR, Acute urinary retention; IPSS, International Prostate Symptom Score.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Multivariate Logistic regression analysis of risk factors for AUR.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="left">Variables</th>
<th valign="middle" align="center">B</th>
<th valign="middle" align="center">SE</th>
<th valign="middle" align="center">OR</th>
<th valign="middle" align="center">CI</th>
<th valign="middle" align="center">Z</th>
<th valign="middle" align="center">P</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">BMI(kg/m^2)</td>
<td valign="middle" align="right">0.17</td>
<td valign="middle" align="right">0.09227</td>
<td valign="middle" align="right">1.186</td>
<td valign="middle" align="left">1.185 (0.990-1.425)</td>
<td valign="middle" align="right">1.845</td>
<td valign="middle" align="right">0.065</td>
</tr>
<tr>
<td valign="middle" align="left">Prostate volume(ml)</td>
<td valign="middle" align="right">0.02</td>
<td valign="middle" align="right">0.00694</td>
<td valign="middle" align="right">1.02</td>
<td valign="middle" align="left">1.020 (1.007-1.035)</td>
<td valign="middle" align="right">2.867</td>
<td valign="middle" align="right">0.004</td>
</tr>
<tr>
<td valign="middle" align="left">Diabetes</td>
<td valign="middle" align="right">0.848</td>
<td valign="middle" align="right">0.40028</td>
<td valign="middle" align="right">2.334</td>
<td valign="middle" align="left">2.334 (1.054-5.125)</td>
<td valign="middle" align="right">2.118</td>
<td valign="middle" align="right">0.034</td>
</tr>
<tr>
<td valign="middle" align="left">constipation</td>
<td valign="middle" align="right">0.894</td>
<td valign="middle" align="right">0.40652</td>
<td valign="middle" align="right">2.444</td>
<td valign="middle" align="left">2.443 (1.090-5.434)</td>
<td valign="middle" align="right">2.198</td>
<td valign="middle" align="right">0.028</td>
</tr>
<tr>
<td valign="middle" align="left">Before biopsy PVR(ml)</td>
<td valign="middle" align="right">0.019</td>
<td valign="middle" align="right">0.00548</td>
<td valign="middle" align="right">1.019</td>
<td valign="middle" align="left">1.019 (1.008-1.030)</td>
<td valign="middle" align="right">3.436</td>
<td valign="middle" align="right">0.001</td>
</tr>
<tr>
<td valign="middle" align="left">IPSS</td>
<td valign="middle" align="right">0.006</td>
<td valign="middle" align="right">0.02788</td>
<td valign="middle" align="right">1.006</td>
<td valign="middle" align="left">1.006 (0.951-1.062)</td>
<td valign="middle" align="right">0.23</td>
<td valign="middle" align="right">0.818</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>AUR, Acute urinary retention; IPSS, International Prostate Symptom Score; PVR, pre-biopsy post-void residual.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3_3">
<title>Modal chart model for estimating the risk of AUR following TP</title>
<p>The enrolled patients were split into training and test groups in a 7:3 ratio using a randomized stratified grouping technique (<xref ref-type="supplementary-material" rid="SM1">
<bold>Supplementary Data</bold>
</xref>). We constructed individualized nomogram estimates to estimate the chance of AUR in patients following TP based on the risk factors determined by binary logistic regression, Boruta feature selection method, and Lasso regression (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>). Each element is assigned a score between 0 and 100 on a modal plot, representing its regression coefficient about the requirement of AUR. Adding the scores related to each component may determine the cumulative score, representing an individual&#x2019;s probability of developing a post-TP AUR. For this calculation, a vertical line from each factor axis intersecting the nomogram&#x2019;s point axis must be drawn. The total score obtained can then be compared to the total score table for explanatory purposes.</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>The probability of AUR in TP patients was predicted using clinical nomograms based on multiple logistic regression analysis and Boruta&#x2019;s algorithm for feature selection. A line was drawn from the matching value to a &#x201c;dot line&#x201d; for every indicator to allocate points. By computing the likelihood of similar &#x201c;totals&#x201d; and using the individual score totals of the six measurements that comprise the nomogram, we can ascertain the patient&#x2019;s risk of AUR. BMI, health index. PVR, post-void residual urine volume. IPSS, International Prostate Symptom Score.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g004.tif">
<alt-text content-type="machine-generated">Nomogram displaying points assigned to factors like BMI, prostate volume, diabetes, constipation, pre-biopsy PVR, and IPSS. It correlates total points to diagnostic probability, aiding in clinical evaluation.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3_4">
<title>Validation of nomogram models</title>
<p>For the training cohort model (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>), the AUC was 0.874 (95% CI: 0.806 &#x2013; 0.9419), and for the testing cohort model (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>), it was 0.898 (0.8218 &#x2013; 0.9741). The results of the training and testing cohorts showed that the model was effective in discriminating between high and low risk patients. The model was well corrected based on the Hosmer-Lemeshow goodness-of-fit test results for the training cohort (&#x3c7;2 = 10.797, P = 0.2135) and validation cohort (&#x3c7;2 = 11568, P = 0.1716). The model&#x2019;s calibration analysis revealed that the model had been calibrated following 500 internal Bootstrap samplings. For the training set (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6A</bold>
</xref>), the Brier score was 0.059 with a p-value of 0.775 (&gt;&#xa0;0.05), and for the validation set (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6B</bold>
</xref>), it was 0.074 with a p-value of 0.697 (&gt; 0.05). The calibration curve revealed a high degree of agreement between the actual likelihood of occurrence and the projected probability.</p>
<fig id="f5" position="float">
<label>Figure&#xa0;5</label>
<caption>
<p>The evaluation and internal validation of the nomogram. <bold>(A)</bold> The AUC of the training group (AUC = 0.874) and <bold>(B)</bold> the validation group (AUC = 0.898) showed that the model had a high discrimination ability.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g005.tif">
<alt-text content-type="machine-generated">Two ROC curve plots, labeled A and B, show sensitivity versus 1-specificity. Curve A has an AUC of 0.874 with a significant point at 0.229 (sensitivity 0.962, specificity 0.755). Curve B has an AUC of 0.898 with a significant point at 0.147 (sensitivity 0.918, specificity 0.848). Both curves are above the diagonal reference line.</alt-text>
</graphic>
</fig>
<fig id="f6" position="float">
<label>Figure&#xa0;6</label>
<caption>
<p>Calibration curves were used to assess the consistency of predicted versus actual risk of AUR following TP. <bold>(A)</bold> calibration curve of the training group and <bold>(B)</bold> calibration curve of the validation group.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g006.tif">
<alt-text content-type="machine-generated">Calibration plots A and B compare predicted probabilities with actual probabilities. Each plot includes three lines: ideal (dashed), apparent (blue), and bias-corrected (red). Both plots show predicted probabilities on the x-axis and actual probabilities on the y-axis. Plot A has a mean absolute error of 0.031 with sample size 419, while plot B has a mean absolute error of 0.025 with sample size 180.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3_5">
<title>Analysis of clinical practicability and rationality of prediction model</title>
<p>We employed the incidence of AUR in patients following TP as a state variable and the predicted probability of the calibration plot as a test variable to evaluate the nomogram&#x2019;s clinical value. As illustrated in <xref ref-type="fig" rid="f7">
<bold>Figure&#xa0;7</bold>
</xref>, we created a clinical decision curve (DCA) for the nomogram model. The Y-axis shows net benefit, whereas the X-axis shows threshold probability. A solid gray line denotes that every patient had AUR, while a narrow solid black line shows that none did. The decision curve indicates that the model is clinically useful throughout a comparatively extensive threshold probability range. In contrast, the red curve shows the advantage for patients utilizing the prediction model for this study. Overall, DCA showed a net clinical benefit of the model over a wide range of thresholds, better than single measures (e.g., IPSS, prostate volume).</p>
<fig id="f7" position="float">
<label>Figure&#xa0;7</label>
<caption>
<p>Clinical decision curves for nomogram models. <bold>(A)</bold> denote the decision curve for the training set, and <bold>(B)</bold> denote the decision curve for the validation set.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g007.tif">
<alt-text content-type="machine-generated">Two line graphs, labeled A and B, show net benefit versus threshold probability. Graph A peaks at a net benefit of 0.1, and Graph B peaks at 0.2. Both graphs use red lines to represent &#x201c;Nomo,&#x201d; gray for &#x201c;All,&#x201d; and black for &#x201c;None.&#x201d; The x-axes are labeled with threshold probability and cost-benefit ratio.</alt-text>
</graphic>
</fig>
<p>We contrasted the ROC curves of the predicted nomograms with those of models that only used one predictor to provide a more thorough assessment. In <xref ref-type="fig" rid="f8">
<bold>Figure&#xa0;8</bold>
</xref>, the nomogram area under the curve (AUR) was more significant than that of BMI, IPSS, pre-biopsy residual urine, and prostate volume alone, indicating the model&#x2019;s plausibility; this suggests that the AUR of individual predictors was consistently smaller than that of the predictive model, highlighting the model&#x2019;s robust performance.</p>
<fig id="f8" position="float">
<label>Figure&#xa0;8</label>
<caption>
<p>Rationality curve analysis of residual variable risk nomogram.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fonc-15-1626529-g008.tif">
<alt-text content-type="machine-generated">ROC curve chart displaying sensitivity against one minus specificity for five variables: Before biopsy PVR in milliliters (red), BMI in kilograms per square meter (green), IPSS (turquoise), Nomo (blue), and prostate volume in milliliters (pink). Each line indicates the diagnostic ability of a test across different cutoff points.</alt-text>
</graphic>
</fig>
</sec>
</sec>
<sec id="s4" sec-type="discussion">
<title>Discussion</title>
<p>Current studies have mostly focused on the comparison of diagnostic accuracy and complication rates between transperineal and transrectal prostate biopsy in the diagnosis of prostate cancer (<xref ref-type="bibr" rid="B27">27</xref>&#x2013;<xref ref-type="bibr" rid="B30">30</xref>). Since template biopsies are carried out more frequently than TRUS biopsies, evaluating any problems and the patient&#x2019;s following effects is critical. Before template biopsy, it is helpful to understand that postoperative complications, counseling, and patient consent are clinically significant risk factors linked with urine retention. According to reports, between 0.10% and 3% of TP biopsies result in infection (<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B31">31</xref>, <xref ref-type="bibr" rid="B32">32</xref>). AUR occurs in 1.5-13% of patients having TP prostate biopsies (<xref ref-type="bibr" rid="B14">14</xref>, <xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B33">33</xref>, <xref ref-type="bibr" rid="B34">34</xref>). Although the frequency of these occurrences has been reported, there is a shortage of information evaluating probable risk factors for infection and AUR following prostate biopsy for TP (<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B14">14</xref>). Predictive models are receiving more attention in several clinical domains, including sepsis, Kawasaki disease, and malignant tumors. Additionally, there is a growing body of pertinent research in these domains (<xref ref-type="bibr" rid="B35">35</xref>&#x2013;<xref ref-type="bibr" rid="B38">38</xref>). For AUR following TP, there aren&#x2019;t many prediction models available yet. Therefore, to support clinical decision-making and offer individualized treatment plans, we set out to create a predictive model for developing AUR following TP surgery.</p>
<p>The clinical information and laboratory parameters of 599 patients who had prostate biopsies were reviewed retrospectively. These included easily accessible laboratory and anthropological data, such as age, sex, BMI, prostate-specific antigen, diabetes, and residual urine before biopsy. We determined the independent variables for AUR in TP patients to be body mass index, prostate volume, history of diabetes, constipation, IPSS, and residual urine before biopsy using various statistical techniques. We created a straightforward and precise nomogram, verified it within the model, and demonstrated its clinically solid applicability and efficacy.</p>
<p>In 14.3% of our cohort, urinary retention happened. Urinary retention has an incidence ranging from 1.6 to 11.4%, according to the NICE guidelines for transperineal template biopsy of the prostate (<xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B33">33</xref>). Pepe et&#xa0;al. (<xref ref-type="bibr" rid="B34">34</xref>) conducted a large single-center study involving 3000 patients with varied amounts of biopsies, and they found a low mean incidence of urine retention of 6.7%. Our rate was compared to other groups (<xref ref-type="bibr" rid="B39">39</xref>), even though it was marginally higher than the incidence reported by NICE, as reported by Merrick et&#xa0;al. Urinary retention occurs 1.7% of the time in patients receiving TRUS biopsy, according to a comprehensive review by Loeb et&#xa0;al. (<xref ref-type="bibr" rid="B11">11</xref>). In contrast to transperineal biopsy, which typically requires at least 24 cores, the conventional protocol for TRUS biopsy only requires 12 cores. Urinary retention can also be prevented by reducing the number of biopsies performed. Taking targeted biopsies instead of entire templates can also save operating time. However, it is contingent upon the operator&#x2019;s cognitive objectives. We selected targeted + systematic access, a total of 16 needles, for patients with apparent targets on MRIs, which may be why the number of biopsy needles we used did not lower the rate of urine retention.</p>
<p>In line with our findings, several studies have found a positive correlation between the frequency of urine retention and the number of needle biopsies performed; however, this relationship was not statistically significant (<xref ref-type="bibr" rid="B33">33</xref>, <xref ref-type="bibr" rid="B34">34</xref>). Urinary retention was linked to a prostate volume of more than 68 milliliters, according to Willis et&#xa0;al. (<xref ref-type="bibr" rid="B22">22</xref>). Increased prostate volume has also been found in several studies to be an independent predictor of AUR diagnosis after TP (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B14">14</xref>). The ratio of the transitional zone volume to the total prostate volume and a greater IPSS are two additional prostate volume markers that may predispose patients to urine retention and worsen LUTS (<xref ref-type="bibr" rid="B11">11</xref>). Urinary retention was significantly predisposed to the severity of LUTS in our study. Furthermore, it has been suggested that more enormous prostate volumes and higher baseline IPSS values may be indicators of LUTS and AUR following PB (<xref ref-type="bibr" rid="B40">40</xref>). Consequently, discussing risk with patients could be considered a preoperative risk factor. Constipation can be regarded as a significant and trustworthy predictor of AUR in individuals receiving transrectal ultrasonography-guided prostate biopsy, according to research by Cahit Sahin et&#xa0;al. (<xref ref-type="bibr" rid="B41">41</xref>). Acute postoperative urine retention has also been described in our community and is also connected with diabetes mellitus and aging (<xref ref-type="bibr" rid="B11">11</xref>). One known consequence of diabetes is neuroautonomic dysfunction, which has been linked to an increased risk of urine retention. According to other research, diagnosing chronic urine retention (CUR) is typically more challenging. It is generally related to higher levels of postvoid residual urine (PVR) (<xref ref-type="bibr" rid="B42">42</xref>), and our data imply that PVR before biopsy is a separate risk factor for AUR following TP. Ultimately, our research revealed that AUR patients&#x2019; BMIs were greater than non-AUR patients. This appears to be a discovery. No study has been done on how BMI affects AUR following TP biopsy. BMI is a little-studied topic, and while we show some intriguing findings, further research is needed to draw firm conclusions.</p>
<p>Existing studies mostly focus on complications after transrectal puncture (TR), there are very few studies on AUR after TP, and most of them are univariate analysis (such as only focusing on prostate volume or number of puncture needles); a few studies involving TP do not establish prediction models and do not include machine learning algorithms to optimize variable screening (<xref ref-type="bibr" rid="B29">29</xref>, <xref ref-type="bibr" rid="B43">43</xref>, <xref ref-type="bibr" rid="B44">44</xref>). As Francesca Kum et&#xa0;al. found factors for urinary retention after transperineal template biopsy of the prostate, but only a univariate association, no predictive model was constructed (<xref ref-type="bibr" rid="B14">14</xref>). Sabri Cavkaytar et&#xa0;al. (<xref ref-type="bibr" rid="B45">45</xref>) used logistic regression to analyze risk factors for postpartum urinary retention, but given the high dimensionality of the data, no further dimensionality reduction was performed using machine learning algorithms. Samuel L Malnik et&#xa0;al. used machine learning to develop a postoperative predictive model for urinary retention after lumbar spine surgery, but only LASSO regression models were used, but often this was not able to eliminate random fluctuations in factor interactions (<xref ref-type="bibr" rid="B46">46</xref>). Moreover, the AUC of our two machine learning algorithms was more significant than that of Ding Xuexuan et&#xa0;al., who identified the core genes of asthma using five machine learning algorithms (<xref ref-type="bibr" rid="B21">21</xref>).</p>
<p>The clinical nomogram of this study integrates biomarkers and clinical characteristics, includes factors such as constipation and BMI in the prediction model of AUR after TP for the first time, and improves the rigor of variable screening through a two-feature selection algorithm to provide a personalized assessment of whether to continue Foley catheter or take additional safety measures to prevent AUR in TP patients. The nomogram constructed in this study is based on six easily accessible clinical measures (body mass index, prostate volume, history of diabetes, constipation, International Prostate Symptom Score, preoperative residual urine volume) that can be directly integrated into the preoperative assessment process of transperineal prostate biopsy (TP). Clinicians achieve precise stratified management by rapidly calculating the patient &#x2018;s acute urinary retention (AUR) risk score: for example, high-risk patients (score &gt; 70%): prophylactic use of alpha-blockers to relax the bladder neck preoperatively, or prolonged monitoring to 72 hours postoperatively, timely detection of signs of urinary retention, and reduction in the risk of complications such as emergency catheterization rate and overdistension of the bladder; for low-risk patients (score &lt; 30%): use a standardized discharge regimen to reduce unnecessary inpatient observation and reduce medical costs while ensuring safety.</p>
<p>The current study has some limitations. It is a single-center cross-sectional study with a limited sample size that may introduce selection bias. In addition, we only performed internal validation on nomogram models, and subsequent studies also required external validation. Furthermore, potential influencing factors such as the number of puncture needles and operator experience were not included, and subsequent studies could expand the range of variables. Subsequent studies can be conducted in a large sample, multicenter, prospective study to find more risk factors for AUR complications in TP patients so that relevant measures can be taken early to avoid repeated catheterization and further hospitalization and improve patient discomfort.</p>
</sec>
</body>
<back>
<sec id="s5" sec-type="data-availability">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="supplementary-material" rid="SM1">
<bold>Supplementary Material</bold>
</xref>. Further inquiries can be directed to the corresponding authors.</p>
</sec>
<sec id="s6" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The studies involving humans were approved by the Medical Ethics Review Committee of the First People &#x2018;s Hospital of Nantong. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants&#x2019; legal guardians/next of kin in accordance with the national legislation and institutional requirements.</p>
</sec>
<sec id="s7" sec-type="author-contributions">
<title>Author contributions</title>
<p>CS: Investigation, Writing &#x2013; original draft. GC: Investigation, Methodology, Writing &#x2013; review &amp; editing. ZC: Investigation, Methodology, Writing &#x2013; review &amp; editing. JY: Investigation, Project administration, Writing &#x2013; review &amp; editing. BZ: Formal Analysis, Investigation, Methodology, Writing &#x2013; review &amp; editing.</p>
</sec>
<sec id="s8" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research and/or publication of this article. The present study was supported by Nantong Minsheng Science and Technology Program (MS22022085), Jiangsu Geriatric Health Research Project (LKM2022059), Yaodong Shenzhou Pharmaceutical Research Capacity Building Fund Project (2024-KY002-01), Nantong University Clinical Medicine Special Scientific Research Fund Project (2024LQ019), and Basic Research and Social Minsheng Plan Project (MS22022085).</p>
</sec>
<sec id="s9" 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="s10" sec-type="ai-statement">
<title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</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>
<sec id="s12" sec-type="supplementary-material">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fonc.2025.1626529/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fonc.2025.1626529/full#supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="Table1.xlsx" id="SM1" mimetype="application/vnd.openxmlformats-officedocument.spreadsheetml.sheet"/>
</sec>
<fn-group>
<title>Abbreviations</title>
<fn fn-type="abbr" id="abbrev1">
<p>TP, Transperineal; TR, Transrectal; LASSO, Least absolute shrinkage and selection operator; PSA, prostate-specific antigen; AUR, Acute urinary retention; IPSS, International Prostate Symptom Score; PVR, Pre-biopsy post-void residual.</p>
</fn>
</fn-group>
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