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<front>
<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>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpsyt.2023.1102258</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>Measuring resilience by cognitive diagnosis models and its prediction of 6-month quality of life in Be Resilient to Breast Cancer (BRBC)</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Liang</surname> <given-names>Mu Zi</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x2020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Chen</surname> <given-names>Peng</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x2020;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1137075/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Knobf</surname> <given-names>M. Tish</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1117705/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Molassiotis</surname> <given-names>Alex</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/731661/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Tang</surname> <given-names>Ying</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1067887/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Hu</surname> <given-names>Guang Yun</given-names></name>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Sun</surname> <given-names>Zhe</given-names></name>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Yu</surname> <given-names>Yuan Liang</given-names></name>
<xref ref-type="aff" rid="aff8"><sup>8</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Ye</surname> <given-names>Zeng Jie</given-names></name>
<xref ref-type="aff" rid="aff9"><sup>9</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/905836/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Guangdong Academy of Population Development</institution>, <addr-line>Guangzhou, Guangdong</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Basic Medical School, Guizhou University of Traditional Chinese Medicine</institution>, <addr-line>Guiyang</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>School of Nursing, Yale University</institution>, <addr-line>Orange, CT</addr-line>, <country>United States</country></aff>
<aff id="aff4"><sup>4</sup><institution>College of Arts, Humanities and Education, University of Derby</institution>, <addr-line>Derby</addr-line>, <country>United Kingdom</country></aff>
<aff id="aff5"><sup>5</sup><institution>Institute of Tumor, Guangzhou University of Chinese Medicine</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country></aff>
<aff id="aff6"><sup>6</sup><institution>School of Nursing, Army Medical University</institution>, <addr-line>Chongqing</addr-line>, <country>China</country></aff>
<aff id="aff7"><sup>7</sup><institution>The First Affiliated Hospital, Guangzhou University of Chinese Medicine</institution>, <addr-line>Guangzhou, Guangdong</addr-line>, <country>China</country></aff>
<aff id="aff8"><sup>8</sup><institution>Mental Health Education and Counseling Center, South China University of Technology</institution>, <addr-line>Guangzhou, Guangdong</addr-line>, <country>China</country></aff>
<aff id="aff9"><sup>9</sup><institution>School of Nursing, Guangzhou University of Chinese Medicine</institution>, <addr-line>Guangzhou, Guangdong</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Daniela Laricchiuta, University of Perugia, Italy</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Wenchao Ma, The University of Alabama, United States; Ho Nam Cheung, The University of Hong Kong, Hong Kong SAR, China</p></fn>
<corresp id="c001">&#x002A;Correspondence: Zeng Jie Ye, <email>zengjieye@qq.com</email></corresp>
<fn fn-type="equal" id="fn002"><p><sup>&#x2020;</sup>These authors have contributed equally to this work and share first authorship</p></fn>
<fn fn-type="other" id="fn004"><p>This article was submitted to Aging Psychiatry, a section of the journal Frontiers in Psychiatry</p></fn>
</author-notes>
<pub-date pub-type="epub">
<day>16</day>
<month>02</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>14</volume>
<elocation-id>1102258</elocation-id>
<history>
<date date-type="received">
<day>18</day>
<month>11</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>01</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2023 Liang, Chen, Knobf, Molassiotis, Tang, Hu, Sun, Yu and Ye.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Liang, Chen, Knobf, Molassiotis, Tang, Hu, Sun, Yu and Ye</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>The application of advanced Cognitive Diagnosis Models (CDMs) in the Patient Reported Outcome (PRO) is limited due to its complex statistics. This study was designed to measure resilience using CDMs and its prediction of 6-month Quality of Life (QoL) in breast cancer.</p>
</sec>
<sec>
<title>Methods</title>
<p>A total of 492 patients were longitudinally enrolled from Be Resilient to Breast Cancer (BRBC) and administered with 10-item Resilience Scale Specific to Cancer (RS-SC-10) and Functional Assessment of Cancer Therapy-Breast (FACT-B). Generalized Deterministic Input, Noisy &#x201C;And&#x201D; Gate (G-DINA) was performed to measure cognitive diagnostic probabilities (CDPs) of resilience. Integrated Discrimination Improvement (IDI) and Net Reclassification Improvement (NRI) were utilized to estimate the incremental prediction value of cognitive diagnostic probabilities over total score.</p>
</sec>
<sec>
<title>Results</title>
<p>CDPs of resilience improved prediction of 6-month QoL above conventional total score. AUC increased from 82.6&#x2013;88.8% to 95.2&#x2013;96.5% in four cohorts (all <italic>P</italic> &#x003C; 0.001). The NRI ranged from 15.13 to 54.01% and IDI ranged from 24.69 to 47.55% (all <italic>P</italic> &#x003C; 0.001).</p>
</sec>
<sec>
<title>Conclusion</title>
<p>CDPs of resilience contribute to a more accurate prediction of 6-month QoL above conventional total score. CDMs could help optimize Patient Reported Outcomes (PROs) measurement in breast cancer.</p>
</sec>
</abstract>
<kwd-group>
<kwd>cognitive diagnosis models (CDMs)</kwd>
<kwd>cognitive diagnostic probabilities</kwd>
<kwd>resilience</kwd>
<kwd>6-month quality of life (QoL)</kwd>
<kwd>breast cancer</kwd>
<kwd>prediction model</kwd>
<kwd>multicenter cohorts</kwd>
</kwd-group>
<counts>
<fig-count count="5"/>
<table-count count="0"/>
<equation-count count="1"/>
<ref-count count="50"/>
<page-count count="9"/>
<word-count count="5344"/>
</counts>
</article-meta>
</front>
<body>
<sec id="S1" sec-type="intro">
<title>Introduction</title>
<p>Breast cancer accounts for 24.5% of all cancer cases in women and 2.3 million new cases are identified worldwide in 2020 (<xref ref-type="bibr" rid="B1">1</xref>). Among which, 18.3% of all breast cancer cases (about 420 thousand) occur in China. In addition, with advances in early detection and new therapies of breast cancer, 5-year survival has increased to near 90% and breast cancer is now treated as a chronic disease (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>). However, breast cancer survivors still suffer from many psychosocial burdens including stigma, depression, anxiety, fear of cancer recurrence, etc., which will result in reduced Quality of Life (QoL) (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B4">4</xref>). Different from physical symptoms (i.e., lymphedema), psychosocial burdens cannot be measured by objective indicators and Patient Reported Outcomes (PROs) are developed to improve the detection of the patients&#x2019; subjective experience (<xref ref-type="bibr" rid="B5">5</xref>). For example, Self-Rating Depression Scale (SDS), the Center for Epidemiologic Studies Depression Scale (CES-D) and the Beck Depression Inventory (BDI) have been well developed to assess the severity of the depressive disorder (<xref ref-type="bibr" rid="B6">6</xref>&#x2013;<xref ref-type="bibr" rid="B8">8</xref>). However, many existing PROs instruments are developed based on classical test theory (CTT) and focus on the accurate estimation of the symptom severity (i.e., depression, fatigue, etc.), which cannot provide detailed information at item-level. For example, most depression inventories are unidimensional and total scores are calculated to estimate the severity of the depressive symptoms with several cutoffs as reference. This procedure is straightforward but item-level information (specific symptom) is neglected, which is not consistent with definition in 10th revision of the International Classification of Diseases (ICD-10) and 5th edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (<xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B10">10</xref>).</p>
<p>Cognitive Diagnosis Models (CDMs), or diagnostic classification models (DCMs), are state of art psychometric models, which have been developed to classify participants into latent classes with unique profiles of attributes (<xref ref-type="bibr" rid="B11">11</xref>). Compared with CTT or item response theory (IRT), the CDMs provide an alternative psychometric framework for test development and score reporting. Due to the complex statistics in CDMs, most CDMs-related articles are published in the field of education measurement. However, multidiscipline researchers have been recently aware of their usefulness in PROs assessments for symptom profiles at item-level, which will be helpful to screening or intervention (<xref ref-type="bibr" rid="B12">12</xref>&#x2013;<xref ref-type="bibr" rid="B14">14</xref>). Further, compared with factor analysis in CCT, CDMs allow latent attributes/symptom criteria to interact resulting in a more flexible psychometric model. Therefore, from a different perspective, the current study was designed to provide more information for the screening and monitoring of resilience as an example under the framework of CDMs. Based on the data from our previous Be Resilient to Breast Cancer (<xref ref-type="bibr" rid="B15">15</xref>&#x2013;<xref ref-type="bibr" rid="B18">18</xref>), the current study was designed to compare the prediction ability of resilience to 6-month Quality of Life (QoL), between total score based on CTT and cognitive diagnostic probabilities (CDPs) based on CDMs. We hypothesized that: (1) CDMs could well extract diagnostic details about patients&#x2019; resilience strengths and weaknesses, (2) CDPs of resilience could offer incremental predictive value above conventional total score.</p>
</sec>
<sec id="S2" sec-type="materials|methods">
<title>Materials and methods</title>
<sec id="S2.SS1">
<title>Patients and data collection</title>
<p>Four cohorts were developed based on our previous Be Resilient to Breast Cancer (BRBC) (<xref ref-type="bibr" rid="B15">15</xref>&#x2013;<xref ref-type="bibr" rid="B18">18</xref>), including: (1) Cohort A, 151 patients were consecutively enrolled from hospital A in Guangzhou between February 2017 and May 2017, (2) Cohort B, 95 patients were consecutively enrolled from hospital B in Foshan between June 2017 and August 2017, (3) Cohort C, 111 patients were consecutively enrolled from hospital C in Jiangmen between July 2017 and September 2017, and (4) Cohort D, 135 patients were consecutively enrolled from hospital D in Zhuhai between September 2017 and November 2017. The enrollment line was described in <xref ref-type="fig" rid="F1">Figure 1A</xref>. The inclusion criteria were: (1) confirmed diagnosis of breast cancer (within 4 weeks), (2) aged &#x003E;18 years, (3) could communicate in Mandarin or Cantonese fluently, and (4) receiving active treatment. The exclusion criteria were: (1) linguistic or intellectual difficulties, (2) had a currently active Axis I psychiatric disorder, (3) life expectancy less than 12 months, and (4) unwilling to participate in the study. The patients were approached by trained research nurses in the current study and baseline information (T0, i.e., demographics, QoL, resilience, etc.) was collected when their informed consent were obtained. Patients can choose telephone or online interview follow-ups (T1, 6-month) when pencil-and-paper test was not available.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption><p><bold>(A)</bold> The enrollment line <bold>(B)</bold> and demographics for patients.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-14-1102258-g001.tif"/>
</fig>
</sec>
<sec id="S2.SS2">
<title>Ethics approval</title>
<p>The current study was part of BRBC trial and ethic approval number was 2016KYTD08. Informed consent was obtained before formal investigation. Other details about BRBC were described elsewhere (<xref ref-type="bibr" rid="B15">15</xref>&#x2013;<xref ref-type="bibr" rid="B18">18</xref>).</p>
</sec>
<sec id="S2.SS3">
<title>Instruments</title>
<sec id="S2.SS3.SSS1">
<title>10-item Resilience Scale Specific to Cancer (RS-SC-10)</title>
<p>The original RS-SC is a 25-item resilience instrument specific to cancer that has five domains of generic element, benefit finding, support and coping, hope for the future, and meaning for existence (<xref ref-type="bibr" rid="B19">19</xref>, <xref ref-type="bibr" rid="B20">20</xref>). RS-SC is rated based on a five-point Likert scale, with higher scores indicating higher resilience levels (score ranges from 25 to 125). In this study, a short-form of 10-item RS-SC (RS-SC-10) was administered (<xref ref-type="bibr" rid="B21">21</xref>&#x2013;<xref ref-type="bibr" rid="B23">23</xref>). RS-SC and RS-SC-10 were attached in the <xref ref-type="supplementary-material" rid="TS1">Supplementary material</xref>.</p>
</sec>
<sec id="S2.SS3.SSS2">
<title>Functional Assessment of Cancer Therapy-Breast (FACT-B)</title>
<p>The Chinese version of FACT-B consists of 37 items and are divided into five domains, including Physical (GP), Social/Family (GS), Emotional (GE), Functional (GF), and Breast Cancer Subscale (BCS) (<xref ref-type="bibr" rid="B24">24</xref>). The total score ranges from 0 to 144 with higher scores indicating better functions. In the current study, the changes of FACT-B between T0 and T1 was used as an anchor against resilience. The change group with loss indicated by &#x2265;0.5 SD (standard deviation) of change was defined as Decreased (outcome = 1) and other groups were defined as Non-decreased (outcome = 0).</p>
</sec>
</sec>
<sec id="S2.SS4">
<title>Statistical analysis</title>
<p>First, based on the two-factor structure of RS-SC-10 in our previous research (<xref ref-type="bibr" rid="B21">21</xref>&#x2013;<xref ref-type="bibr" rid="B23">23</xref>), two theory-based Q matrix were developed for validating the number of item attributes and detecting the misidentified elements, including a bifactor Q-matrix and a non-bifactor one (<xref ref-type="fig" rid="F2">Figures 2A, B</xref>). A cell with the value of 1 indicates that the corresponding item attribute is captured by the corresponding item.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption><p>Q-matrix comparison and validation. <bold>(A)</bold> A non-bifactor Q-matrix, <bold>(B)</bold> a bifactor Q-matrix, <bold>(C)</bold> heatmaps for adjusted <italic>p</italic>-values of transformed correlation, and <bold>(D)</bold> mesa plots mapping attributes to items.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-14-1102258-g002.tif"/>
</fig>
<p>Second, an unrestricted and saturated model named as Generalized Deterministic Input, Noisy &#x201C;And&#x201D; Gate (G-DINA) was utilized in the current study with two different Q matrix to avoid potential model misspecifications. The item response function (IRF) of G-DINA was detailed as below (<xref ref-type="bibr" rid="B25">25</xref>):</p>
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<mml:mo>&#x2032;</mml:mo>
</mml:msup>
</mml:mrow>
</mml:msub>
</mml:mrow>
</mml:math>
</disp-formula>
<p>where <italic>g</italic>[&#x22C5;] represents an identity, logit, or log link function, &#x03B4;<sub><italic>j</italic>0</sub> is the intercept of item <italic>j</italic>, &#x03B4;<italic><sub><italic>jk</italic></sub></italic> is the main effect of attribute <italic>k</italic>, &#x03B4;<sub><italic>jkk</italic>&#x2019;</sub> is the two-way interaction effect of attributes <italic>k</italic> and <italic>k</italic>&#x2032;, and &#x03B4;<sub><italic>j</italic>12.<italic>Kj&#x002A;</italic></sub> is <italic>Kj</italic>&#x002A;-way interaction effect of attributes 1 to <italic>Kj</italic>&#x002A;. In addition, a higher-order 2PL model was chosen for the attribute distribution and monotonic constraints was also applied in the G-DINA model.</p>
<p>Third, relative-fit statistics including Akaike Information Criterion (AIC), Bayesian Information Criterion (BIC), Consistent AIC (CAIC), Sample Adjusted BIC (SABIC), as well as a likelihood ratio (LR) test were compared between the two models with different Q matrix (<xref ref-type="bibr" rid="B26">26</xref>). In addition, absolute-fit statistics including Second-order Marginal Statistic (M2, less is better), Root Mean Square Error of Approximation (RMSEA, RMSEA &#x003C; 0.045 is defined as a good fit) and Standardized Mean Square Root of Squared Residuals (SRMSR, SRMSR &#x003C; 0.05 is defined as a good fit) were also considered (<xref ref-type="bibr" rid="B26">26</xref>). Further, a heatmap for residuals between the observed and predicted correlations of item pairs was checked and the optimal G-DINA model was retained for further model evaluation (<xref ref-type="bibr" rid="B27">27</xref>).</p>
<p>Fourth, Q-matrix was validated by mesa plots mapping attributes to items (<xref ref-type="bibr" rid="B28">28</xref>). The cutoff of Proportion of Variance Accounted For (PVAF) by a particular q-vector was set at 0.95.</p>
<p>Fifth, item parameter including success probabilities of reduced latent classes, guessing and slip parameters, delta parameters, and success probabilities of all latent classes with or without standard errors (SEs) were estimated in the G-DINA model (<xref ref-type="bibr" rid="B25">25</xref>).</p>
<p>Sixth, success probabilities of attributes for each person were extracted from the G-DINA model and two models, Model 1: (TNM stage + Total Score) vs. Model 2: (TNM stage + Cognitive Diagnostic Probabilities, were compared based on indicators of AUC, NRI (Net Reclassification Improvement), IDI (Integrated Discrimination Improvement), calibration curves (estimated by Brier score), and Decision Curve Analysis (<xref ref-type="bibr" rid="B29">29</xref>, <xref ref-type="bibr" rid="B30">30</xref>). In addition, Clinical Impact Curve were also estimated to evaluate Model 2&#x2032; clinical utilizations (<xref ref-type="bibr" rid="B31">31</xref>).</p>
<p>At last, Wald test was performed to compare G-DINA model against other reduced model (i.e., DINA, DINO, etc.) at the item level, which could provide better classification results without losing significant fits to models (<xref ref-type="bibr" rid="B32">32</xref>). All statistical analyses were performed by GDINA R Package (<xref ref-type="bibr" rid="B33">33</xref>).</p>
</sec>
</sec>
<sec id="S3" sec-type="results">
<title>Results</title>
<sec id="S3.SS1">
<title>Demographics</title>
<p>Overall, 151, 95, 111, 135 patients were enrolled from four different cohorts. Finally, 145 (96.0%), 86 (90.5%), 104 (93.7%),123 (91.1%) patients completed 6-month follow-up assessments at T1 and a total of 458 patients were analyzed. Compared to those enrolled in the analysis, patients lost to follow-up were reported to have more combordities (<italic>P</italic> = 0.078) and no other significant demographics were identified. The baseline characteristics of the patients were summarized in <xref ref-type="fig" rid="F1">Figure 1B</xref>.</p>
</sec>
<sec id="S3.SS2">
<title>Q-matrix comparison and validation</title>
<p>Two theory-based Q matrix were developed for validating the number of item attributes and detecting the misidentified elements, including a non-bifactor Q-matrix (Model 1, <xref ref-type="fig" rid="F2">Figure 2A</xref>) and a bifactor one (Model 2, <xref ref-type="fig" rid="F2">Figure 2B</xref>). It demonstrated that Model 2 had better fitting indicators in terms of Relative-fit Statistics (i.e., AIC = 4899.073 vs. 5121.619, BIC = 5090.294 vs. 5221.386, etc.) and Absolute-fit Statistics (i.e., RMSEA = 0.0386 vs. 0.0589, SRMSR = 0.0321 vs. 0.0881, etc.) compared to those based on Model 1. The LR test also confirmed these findings (<italic>X</italic><sup>2</sup> = 266.544, df = 24, <italic>P</italic> &#x003C; 0.0001). In addition, the heatmap for Model 1 demonstrated that residuals between the observed and predicted correlations of item pairs were significant resulting in misfitting (<xref ref-type="fig" rid="F2">Figure 2C</xref>, adjusted <italic>P</italic>-value for transformed correlation = 0.0058). Thus, Model 2 was chosen for further Q-matrix validation. Based on the cutoff of 0.95 of PVAF, mesa plots were provided for mapping attributes to items and no changes should be made to all 10 items. Full details about different q-vectors were described in <xref ref-type="fig" rid="F2">Figure 2D</xref>.</p>
</sec>
<sec id="S3.SS3">
<title>Item parameter estimation</title>
<p>At the item-level, guessing (<italic>g</italic>) and slip (<italic>s</italic>) parameters with SEs were presented in <xref ref-type="fig" rid="F3">Figure 3A</xref>, indicating the lower (<italic>g</italic>) and upper bound (<italic>1-s</italic>) of success probabilities. In addition, delta parameters (&#x03B4;) for IRF of G-DINA, and success probabilities of all latent classes (i.e., 000, 100, 010, etc.) were also presented in <xref ref-type="fig" rid="F3">Figure 3A</xref>. The distributions of the success probability across all reduced latent classes in each item were drawn in <xref ref-type="fig" rid="F3">Figure 3B</xref>. It showed that an increase was observed in the success probability as a patient mastered more attributes in most items (i.e., item 8, 9, 10, etc.) indicating a perfect fitting. At the test-level, 67.6, 41.3, 45.6% of patients successfully mastered &#x201C;Generic Elements (A1),&#x201D; &#x201C;Shift-Persist (A2),&#x201D; &#x201C;General Factor (A3)&#x201D; which were described in <xref ref-type="fig" rid="F3">Figure 3C</xref>. In addition, the most proportions of latent classes were &#x201C;111,&#x201D; &#x201C;100,&#x201D; and &#x201C;000,&#x201D; accounting for 30.0, 27.2, 22.0% of the patients, respectively. Other details about latent classes could be identified in <xref ref-type="fig" rid="F3">Figure 3D</xref>. The accuracy at test level was 0.8377 and were 0.9528 (A1), 0.9042 (A2), and 0.9155 (A3) at attribute level, respectively.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption><p>Item parameter estimation. <bold>(A)</bold> Item parameter estimation, <bold>(B)</bold> success probabilities distribution, <bold>(C)</bold> mastery attributes distribution, and <bold>(D)</bold> latent classes distribution.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-14-1102258-g003.tif"/>
</fig>
</sec>
<sec id="S3.SS4">
<title>The comparison of different prediction models (total score vs. cognitive diagnostic probabilities)</title>
<p>Two models were developed to construct the prediction model for Decreased QoL outcome, including: Model 1: TNM stage + Total Score and Model 2: TNM stage + Cognitive Diagnostic Probabilities. Compared with Model 1, AUC in Model 2 increased from 82.6&#x2013;88.8 to 95.2&#x2013;96.5% in four cohorts (all <italic>P</italic> &#x003C; 0.001, <xref ref-type="fig" rid="F4">Figure 4A</xref>). The NRI in Model 2 ranged from 15.13 to 54.01% and IDI ranged from 24.69 to 47.55% (all <italic>P</italic> &#x003C; 0.0001, <xref ref-type="fig" rid="F4">Figure 4A</xref>). In addition, Brier scores in Model 2 ranged from 7.8 to 10.2, which were significantly less than those in Model 1 (ranged from 14.1 to 20.9, <xref ref-type="fig" rid="F4">Figure 4B</xref>). DCA indicated that Model 2 showed higher net benefits compared with Model 1 (<xref ref-type="fig" rid="F4">Figure 4C</xref>) in different cohorts. Thus, Model 2 had better predictable ability to Decreased QoL outcome than Model 1 and CICs about Model 2&#x2032; clinical utilization in different cohorts were detailed in <xref ref-type="fig" rid="F4">Figure 4D</xref>.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption><p>The comparison of different prediction models (total score vs. cognitive diagnostic probabilities). <bold>(A)</bold> Area under curve, net reclassification improvement and integrated discrimination improvement in Model 1 and Model 2, <bold>(B)</bold> calibration curves in Model 1 and Model 2, <bold>(C)</bold> decision curve analysis in Model 1 and Model 2, and <bold>(D)</bold> clinical impact curves in Model 1 and Model 2.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-14-1102258-g004.tif"/>
</fig>
</sec>
<sec id="S3.SS5">
<title>Item-level model comparison</title>
<p>Wald test indicated that the DINA model could be replaced by several reduced cognitive diagnostic models. For example, in item 1, 3, and 6, Linear Logistic Model (LLM) could provide better classification results without losing significant fits to models. Other information about Additive Cognitive Diagnosis Model (ACDM) and Reduced Reparameterized Unified Model (RRUM) could be recognized in <xref ref-type="fig" rid="F5">Figure 5</xref>.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption><p>Item-level model comparison.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-14-1102258-g005.tif"/>
</fig>
</sec>
</sec>
<sec id="S4" sec-type="discussion">
<title>Discussion</title>
<p>This is the first study to measure resilience by CDMs and its prediction of 6-month Quality of Life (QoL) in breast cancer, though CDMs have been performed to analyze PROs in pathological gambler, schizophrenia, internet addition, etc (<xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B34">34</xref>). The findings demonstrated in this manuscript confirmed the usefulness of CDMs as a sophisticated method for jointly performing resilience assessment and investigating theory-based structural facets of resilience traits. With the additional item-level information from G-DINA model, the prediction ability of resilience to 6-month QoL was significantly enhanced. Thus, the underlying structure of resilience traits or other psychological indicators (i.e., depression, anxiety, etc.) should also be considered in future PROs research. Furthermore, G-DINA-based RS-SC-10 could reduce the burden of psychologist/psychiatrist when large patients are screened or monitored.</p>
<p>However, two important issues in the application of CDMs should be discussed here. First, a theoretical framework or Q matrix should be set for CDMs before the formal analysis and the results will have limited diagnostic information if the theoretical framework is not relevant to the diagnosis. For example, based on our previous study, two theory-based Q matrix were developed for validating the number of item attributes and detecting the misidentified elements, including a non-bifactor Q-matrix (Model 1, <xref ref-type="fig" rid="F2">Figure 2A</xref>) and a bifactor one (Model 2, <xref ref-type="fig" rid="F2">Figure 2B</xref>). If both Q matrix are biased, misguided Q-matrices will lead to meaningless results with inflated slip and guess parameters, high RMSE and low Monte Carlo <italic>p</italic>-values. However, there exists no golden standard/definition for resilience and whether resilience should be conceptualized as a trait or a state is also debated (<xref ref-type="bibr" rid="B35">35</xref>&#x2013;<xref ref-type="bibr" rid="B37">37</xref>). Therefore, we should be cautious about the exploratory Q matrix-based findings derived from the current study which should be replicated and validated in future research. Also, Q-matrix discovery techniques have been developed to handle with the issue about unknown Q-matrix. For example, a Q-matrix discovery method has been developed to allows for uncertainty in instrument development process by using experts&#x2019; comments in a Bayesian algorithm (<xref ref-type="bibr" rid="B38">38</xref>).</p>
<p>Second, the cognitive diagnostic probabilities (CDPs) should be validated by external indicators. In the current study, CDPs of resilience were anchored against 6-month QoL based on a prospective cohort design. However, researchers might prefer that external validation come not only from PRO instruments but also from diagnoses elicited from trained physicians. More objective indicators, i.e., cortisol, C-reactive protein, systolic pressure, etc., can be incorporated into the CDMs research, which will give more confidence to the interpretation of results (<xref ref-type="bibr" rid="B39">39</xref>, <xref ref-type="bibr" rid="B40">40</xref>). In addition, we should be noted that CDMs take complex interactions among latent variables into consideration which allows greater flexibility than most IRT models in modeling item responses. However, this also results in complex model with too many parameters. In the current study, several reduced models have been recommended for replacing G-DINA (<xref ref-type="fig" rid="F5">Figure 5</xref>) and these models can be tried in the future research to obtain more stable parameter estimates. At last, if a long item instrument with many attributes is administered in a large sample, computerized adaptive testing (CAT) can be considered to reduce the test time without a loss of measurement precision. Some research on combining CDMs and CAT has been explored in the field of psychometrics and CDMs-CAT is promising in the field of medicine (<xref ref-type="bibr" rid="B41">41</xref>, <xref ref-type="bibr" rid="B42">42</xref>).</p>
</sec>
<sec id="S5">
<title>Limitation</title>
<p>There are several limitations should be considered. First, many parameters are involved in G-DINA and the sample size in the current study may not be large enough resulting in potential biased estimation of Wald test for model selection or DIF detection (<xref ref-type="bibr" rid="B43">43</xref>). Larger sample should be considered in future research to get a robust estimated covariance matrix. Second, our sample was collected from an extremely narrow Chinese population with breast cancer and the generalizability of these findings should be further validated in other populations (i.e., lung cancer, colon-rectal cancer, etc.). In addition, CDMs allow for measurement of differences in attribute patterns cross-culturally which can help explain how cultural differences are manifested in the patterns of attributes mastered (<xref ref-type="bibr" rid="B44">44</xref>, <xref ref-type="bibr" rid="B45">45</xref>). Third, RS-SC-10 has been validated in family caregivers (i.e., parents of children with cancer) as well as patients with different cancer types, and CDMs might also have great potentials in these vulnerable populations (<xref ref-type="bibr" rid="B46">46</xref>&#x2013;<xref ref-type="bibr" rid="B50">50</xref>). More CDM-based evaluation and intervention for these vulnerable groups are urgently warranted. At last, although various CDMs have been developed to detect mastery and non-mastery of multiple fine-grained skills or attributes (i.e., DINO, DINA, ACDM, RRUM, etc.), most researchers in the field of medicine are still not familiar with CDMs due to their novelty as well as complex statistics. There exist several software programs available to estimate CDMs, for example, several R packages are available for the CDMs analyses. However, syntax preparation of these programs requires researchers&#x2019; substantial effort and more easy-use software should be developed to facilitate the application of CDMs.</p>
</sec>
<sec id="S6" sec-type="conclusion">
<title>Conclusion</title>
<p>Cognitive diagnostic probabilities of resilience contribute to a more accurate prediction of 6-month QoL above conventional total score. CDMs could help optimize Patient Reported Outcomes (PROs) measurement in breast cancer.</p>
</sec>
<sec id="S7" 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="S8" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The studies involving human participants were reviewed and approved by Guangzhou University of Chinese Medicine. The patients/participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="S9" sec-type="author-contributions">
<title>Author contributions</title>
<p>ML and PC: investigation, formal analysis, supervision, and writing&#x2014;original draft. MK and AM: methodology and writing&#x2014;review and editing. YT: investigation and visualization. GH and ZS: investigation. YY: data curation and software. ZY: conceptualization, funding acquisition, project administration, resources, and writing&#x2014;review and editing. All authors contributed to the article and approved the submitted version.</p>
</sec>
</body>
<back>
<sec id="S10" sec-type="funding-information">
<title>Funding</title>
<p>This research was funded by grants from National Natural Science Foundation of China (Nos. 72274043 and 71904033), Young Elite Scientists Sponsorship Program by CACM (No. 2021-QNRC2-B08), Humanity and Social Science Foundation of Department of Education of Guangdong Province (No. 2020WTSCX009), Humanity and Social Science Foundation of Guangzhou (No. 2021GZGJ57), Guangdong Research Center for TCM Service and Industrial Development, Guangzhou University of Chinese Medicine (No. 2022ZDA03), and Humanity and Social Science Foundation of Guangzhou University of Chinese Medicine (No. 2021SKYB07).</p>
</sec>
<sec id="S11" 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="S12" 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="S13" 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/fpsyt.2023.1102258/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fpsyt.2023.1102258/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Table_1.DOCX" id="TS1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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