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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JMIR</journal-id>
      <journal-id journal-id-type="nlm-ta">J Med Internet Res</journal-id>
      <journal-title>Journal of Medical Internet Research</journal-title>
      <issn pub-type="epub">1438-8871</issn>
      <publisher>
        <publisher-name>JMIR Publications</publisher-name>
        <publisher-loc>Toronto, Canada</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">v23i2e20298</article-id>
      <article-id pub-id-type="pmid">33625369</article-id>
      <article-id pub-id-type="doi">10.2196/20298</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Paper</subject>
        </subj-group>
        <subj-group subj-group-type="article-type">
          <subject>Original Paper</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>A Risk Prediction Model Based on Machine Learning for Cognitive Impairment Among Chinese Community-Dwelling Elderly People With Normal Cognition: Development and Validation Study</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Eysenbach</surname>
            <given-names>Gunther</given-names>
          </name>
        </contrib>
        <contrib contrib-type="editor">
          <name>
            <surname>Zeng</surname>
            <given-names>Qing</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Ling</surname>
            <given-names>Xuefeng</given-names>
          </name>
        </contrib>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Li</surname>
            <given-names>Chen</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib id="contrib1" contrib-type="author">
          <name name-style="western">
            <surname>Hu</surname>
            <given-names>Mingyue</given-names>
          </name>
          <degrees>MSc</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-2052-6643</ext-link>
        </contrib>
        <contrib id="contrib2" contrib-type="author">
          <name name-style="western">
            <surname>Shu</surname>
            <given-names>Xinhui</given-names>
          </name>
          <degrees>MSc</degrees>
          <xref rid="aff2" ref-type="aff">2</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-5380-426X</ext-link>
        </contrib>
        <contrib id="contrib3" contrib-type="author">
          <name name-style="western">
            <surname>Yu</surname>
            <given-names>Gang</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff3" ref-type="aff">3</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-3599-8985</ext-link>
        </contrib>
        <contrib id="contrib4" contrib-type="author">
          <name name-style="western">
            <surname>Wu</surname>
            <given-names>Xinyin</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff4" ref-type="aff">4</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-3772-2376</ext-link>
        </contrib>
        <contrib id="contrib5" contrib-type="author" equal-contrib="yes">
          <name name-style="western">
            <surname>Välimäki</surname>
            <given-names>Maritta</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <xref rid="aff5" ref-type="aff">5</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-3124-9290</ext-link>
        </contrib>
        <contrib id="contrib6" contrib-type="author" corresp="yes" equal-contrib="yes">
          <name name-style="western">
            <surname>Feng</surname>
            <given-names>Hui</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff1" ref-type="aff">1</xref>
          <address>
            <institution>Xiangya Nursing School</institution>
            <institution>Central South University</institution>
            <addr-line>Yuelu District</addr-line>
            <addr-line>172 Tongzipo Road</addr-line>
            <addr-line>Changsha </addr-line>
            <country>China</country>
            <phone>86 15173121969</phone>
            <email>feng.hui@csu.edu.cn</email>
          </address>
          <xref rid="aff6" ref-type="aff">6</xref>
          <xref rid="aff7" ref-type="aff">7</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0001-6930-4780</ext-link>
        </contrib>
      </contrib-group>
      <aff id="aff1">
        <label>1</label>
        <institution>Xiangya Nursing School</institution>
        <institution>Central South University</institution>
        <addr-line>Changsha</addr-line>
        <country>China</country>
      </aff>
      <aff id="aff2">
        <label>2</label>
        <institution>Henan Cancer Hospital Province</institution>
        <institution>Zhengzhou University</institution>
        <addr-line>Zhengzhou</addr-line>
        <country>China</country>
      </aff>
      <aff id="aff3">
        <label>3</label>
        <institution>Department of Biomedical Engineering</institution>
        <institution>School of Basic Medical Science</institution>
        <institution>Central South University</institution>
        <addr-line>Changsha</addr-line>
        <country>China</country>
      </aff>
      <aff id="aff4">
        <label>4</label>
        <institution>Xiangya School of Public Health</institution>
        <institution>Central South University</institution>
        <addr-line>Changsha</addr-line>
        <country>China</country>
      </aff>
      <aff id="aff5">
        <label>5</label>
        <institution>Department of Nursing Science</institution>
        <institution>University of Turku</institution>
        <addr-line>Helsinki</addr-line>
        <country>Finland</country>
      </aff>
      <aff id="aff6">
        <label>6</label>
        <institution>Oceanwide Health Management Institute</institution>
        <institution>Central South University</institution>
        <addr-line>Changsha</addr-line>
        <country>China</country>
      </aff>
      <aff id="aff7">
        <label>7</label>
        <institution>National Clinical Research Center for Geriatric Disorders</institution>
        <institution>Xiangya Hospital</institution>
        <institution>Central South University</institution>
        <addr-line>Changsha</addr-line>
        <country>China</country>
      </aff>
      <author-notes>
        <corresp>Corresponding Author: Hui Feng <email>feng.hui@csu.edu.cn</email></corresp>
      </author-notes>
      <pub-date pub-type="collection">
        <month>2</month>
        <year>2021</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>24</day>
        <month>2</month>
        <year>2021</year>
      </pub-date>
      <volume>23</volume>
      <issue>2</issue>
      <elocation-id>e20298</elocation-id>
      <history>
        <date date-type="received">
          <day>15</day>
          <month>5</month>
          <year>2020</year>
        </date>
        <date date-type="rev-request">
          <day>28</day>
          <month>8</month>
          <year>2020</year>
        </date>
        <date date-type="rev-recd">
          <day>14</day>
          <month>1</month>
          <year>2021</year>
        </date>
        <date date-type="accepted">
          <day>18</day>
          <month>1</month>
          <year>2021</year>
        </date>
      </history>
      <copyright-statement>©Mingyue Hu, Xinhui Shu, Gang Yu, Xinyin Wu, Maritta Välimäki, Hui Feng. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 24.02.2021.</copyright-statement>
      <copyright-year>2021</copyright-year>
      <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
        <p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.</p>
      </license>
      <self-uri xlink:href="https://www.jmir.org/2021/2/e20298" xlink:type="simple"/>
      <abstract>
        <sec sec-type="background">
          <title>Background</title>
          <p>Identifying cognitive impairment early enough could support timely intervention that may hinder or delay the trajectory of cognitive impairment, thus increasing the chances for successful cognitive aging.</p>
        </sec>
        <sec sec-type="objective">
          <title>Objective</title>
          <p>We aimed to build a prediction model based on machine learning for cognitive impairment among Chinese community-dwelling elderly people with normal cognition.</p>
        </sec>
        <sec sec-type="methods">
          <title>Methods</title>
          <p>A prospective cohort of 6718 older people from the Chinese Longitudinal Healthy Longevity Survey (CLHLS) register, followed between 2008 and 2011, was used to develop and validate the prediction model. Participants were included if they were aged 60 years or above, were community-dwelling elderly people, and had a cognitive Mini-Mental State Examination (MMSE) score ≥18. They were excluded if they were diagnosed with a severe disease (eg, cancer and dementia) or were living in institutions. Cognitive impairment was identified using the Chinese version of the MMSE. Several machine learning algorithms (random forest, XGBoost, naïve Bayes, and logistic regression) were used to assess the 3-year risk of developing cognitive impairment. Optimal cutoffs and adjusted parameters were explored in validation data, and the model was further evaluated in test data. A nomogram was established to vividly present the prediction model.</p>
        </sec>
        <sec sec-type="results">
          <title>Results</title>
          <p>The mean age of the participants was 80.4 years (SD 10.3 years), and 50.85% (3416/6718) were female. During a 3-year follow-up, 991 (14.8%) participants were identified with cognitive impairment. Among 45 features, the following four features were finally selected to develop the model: age, instrumental activities of daily living, marital status, and baseline cognitive function. The concordance index of the model constructed by logistic regression was 0.814 (95% CI 0.781-0.846). Older people with normal cognitive functioning having a nomogram score of less than 170 were considered to have a low 3-year risk of cognitive impairment, and those with a score of 170 or greater were considered to have a high 3-year risk of cognitive impairment.</p>
        </sec>
        <sec sec-type="conclusions">
          <title>Conclusions</title>
          <p>This simple and feasible cognitive impairment prediction model could identify community-dwelling elderly people at the greatest 3-year risk for cognitive impairment, which could help community nurses in the early identification of dementia.</p>
        </sec>
      </abstract>
      <kwd-group>
        <kwd>prediction model</kwd>
        <kwd>cognitive impairment</kwd>
        <kwd>machine learning</kwd>
        <kwd>nomogram</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="introduction">
      <title>Introduction</title>
      <p>Dementia constitutes a major health care burden nationally and worldwide [<xref ref-type="bibr" rid="ref1">1</xref>]. Approximately every 3 seconds, a person somewhere in the world is diagnosed with dementia, and the current annual cost of dementia is estimated to be US $1 trillion, which is set to double by 2030 [<xref ref-type="bibr" rid="ref2">2</xref>]. China has the largest population of patients with dementia in the world (9.5 million) followed by the United States (4.2 million) [<xref ref-type="bibr" rid="ref1">1</xref>]. Evidence suggests that delaying the onset of dementia by 1 year is likely to reduce its prevalence by 11% by 2050, while delaying it by 5 years could halve the number of people living with dementia by 2050 [<xref ref-type="bibr" rid="ref3">3</xref>]. Given that dementia is incurable, it is of high importance to detect cognitive impairment in its early stages [<xref ref-type="bibr" rid="ref4">4</xref>].</p>
      <p>Good evidence already exists that specific risk factors can contribute to increased dementia risk at different life stages. The risk factors are education in early life, hypertension and obesity in midlife, and smoking and depression in later life [<xref ref-type="bibr" rid="ref5">5</xref>]. Prediction models concerning risk factors for cognitive impairment have already been published. However, the variables included in the models vary, and they mostly focus on laboratory markers only [<xref ref-type="bibr" rid="ref6">6</xref>-<xref ref-type="bibr" rid="ref8">8</xref>]. A systematic review by Hou et al included 61 studies of the prediction models of dementia. They found that age, sex, education, cognition assessment scales, BMI, alcohol intake, and genetic variables were the most common predictors included in the models [<xref ref-type="bibr" rid="ref8">8</xref>]. Questionnaire-based data have also been used to explore the clinical variables with promising predictive values in the transition to cognitive impairment (demographic characteristics and neuropsychiatric symptoms). Other studies have used data based on medical imaging (brain atrophy), genes (apolipoprotein Eε4), or biomarkers (amyloid-β, tau, etc) [<xref ref-type="bibr" rid="ref5">5</xref>,<xref ref-type="bibr" rid="ref9">9</xref>,<xref ref-type="bibr" rid="ref10">10</xref>]. One study used the C-Pittsburgh compound B (C-PiB) medial temporal standard uptake value ratio with the Mini-Mental State Examination (MMSE) for the prediction of a person going from mild cognitive impairment to dementia, and the area under the curve was 0.92 [<xref ref-type="bibr" rid="ref6">6</xref>]. Kivipelto et al used big data to develop a prediction model of the risk of late-life dementia in middle-aged people, and the model included age, education, hypertension, hypercholesterolemia, and obesity as variables, with an average area under the curve of 0.77 [<xref ref-type="bibr" rid="ref7">7</xref>]. However, these prediction models are complex, less accurate, and difficult to implement in practice for nursing staff who are working with elderly patients. Therefore, especially for use in community environments, simpler, more accurate, and feasible models are needed [<xref ref-type="bibr" rid="ref8">8</xref>].</p>
      <p>Machine learning has recently been used to produce a prediction model for practice. Machine learning can help in modeling information based on causal and/or statistical data, potentially revealing hidden dependencies between factors and diseases in a big data environment [<xref ref-type="bibr" rid="ref11">11</xref>]. Published studies show how machine learning algorithms, such as naïve Bayes (NB), AdaBoost, and random forest (RF), have been used to predict or detect cognitive impairment [<xref ref-type="bibr" rid="ref12">12</xref>-<xref ref-type="bibr" rid="ref15">15</xref>].</p>
      <p>We systematically searched PubMed ([“cognitive impairment” OR “cognitive decline” OR “dementia” OR “alzheimer*”] AND [“machine learning” OR “data mining” OR “big data”] AND “prediction”) and found four studies in which machine learning was used to identify risk factors for dementia among people with normal cognition at baseline. One study [<xref ref-type="bibr" rid="ref16">16</xref>] used unsupervised machine learning to develop a dementia prediction model that could identify people at a high risk of developing dementia. Another study [<xref ref-type="bibr" rid="ref13">13</xref>] used the medical records of 93,120 patients to develop a model for exploring undetected dementia using a machine learning approach (with an area under the curve of 0.74). One study [<xref ref-type="bibr" rid="ref17">17</xref>] developed a model for predicting the risk of developing dementia within the next 2 years among older people (aged 85 years or above) without dementia (with an area under the curve of 0.73). The study showed that the predictors differed between the youngest and oldest individuals in the population. Further, another study used supervised machine learning to develop a dementia prediction model (area under the curve values of 0.75 and 0.79) and found that the Disease State Index is useful for identifying individuals who are most at risk [<xref ref-type="bibr" rid="ref18">18</xref>].</p>
      <p>However, a variety of difficulties have been identified in implementing the results of machine learning in clinical practice, as the data have been collected at one time point only, meaning that the causality of the data can be questioned [<xref ref-type="bibr" rid="ref13">13</xref>]. Some prediction models have been too complicated, and there have been problems with accuracy in the prediction [<xref ref-type="bibr" rid="ref16">16</xref>-<xref ref-type="bibr" rid="ref18">18</xref>]. In addition, although the results seem to be acceptable from a statistical point of view, understanding the interpretation of the unsupervised machine learning result and its implementation into practice is demanding [<xref ref-type="bibr" rid="ref16">16</xref>]. There is still room for the improvement of prediction models for forecasting risks for dementia. In addition, more studies are needed to develop and translate the results into clinical practice, especially for community environments [<xref ref-type="bibr" rid="ref19">19</xref>]. We therefore aimed to develop an algorithm to be used in a prediction model to identify risk factors for cognitive impairment among Chinese community-dwelling elderly people with normal cognition. The study results are important, as an approach to stratify the individual risks for cognitive impairment is needed in community settings for both national and international purposes [<xref ref-type="bibr" rid="ref20">20</xref>].</p>
    </sec>
    <sec sec-type="methods">
      <title>Methods</title>
      <sec>
        <title>Design and Participants</title>
        <p>This study strictly followed the Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis (TRIPOD): The TRIPOD Statement [<xref ref-type="bibr" rid="ref21">21</xref>]. In this machine learning approach, the national prospective longitudinal results of the Chinese Longitudinal Healthy Longevity Survey (CLHLS) were used [<xref ref-type="bibr" rid="ref22">22</xref>]. The CLHLS is one of the largest national longitudinal studies for investigating the health of older Chinese adults. Launched in 1998, the CLHLS implemented follow-up surveys in 2000, 2002, 2005, 2008-09, 2011-12, and 2014. A total of 22 Chinese provinces were randomly recruited, and the sampling frame covered about 85% of the total population of China. The survey results in the national database are freely accessible and available online [<xref ref-type="bibr" rid="ref23">23</xref>]. The 2008-09 survey included a total of 16,954 participants.</p>
        <p>We included 11,788 participants from the 2008-09 wave, and 6718 participants were eligible for model development and internal validation. Participants were included if they were (1) aged 60 years or above; (2) community-dwelling elderly people; and (3) normally cognitive (MMSE score ≥18). They were excluded if they (1) were diagnosed with a severe disease (eg, cancer and dementia) or (2) lived in an institution. A detailed flow chart of participant selection is shown in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>. Among the remaining participants, in the 2011-12 wave, a total of 1913 participants were lost in the follow-up and 2879 died. Those who were excluded from analyses owing to nonparticipation or death were on average older (<italic>P</italic>&#60;.001) and had lower physical function scores (<italic>P</italic>&#60;.001) and lower baseline cognition scores (<italic>P</italic>&#60;.001). The two groups were not significantly different in terms of sex (<italic>P</italic>=.45).</p>
      </sec>
      <sec>
        <title>Outcome Variables and Predictors</title>
        <p>Cognitive impairment was defined by the Chinese version of the Mini-Mental State Examination (CMMSE) [<xref ref-type="bibr" rid="ref24">24</xref>], which was culturally translated from the international standard of the MMSE questionnaire. The CMMSE contains 24 items within six dimensions (five items for orientation, three for registration, one for naming, five for attention and calculation, three for recall, and seven for language). The score of the Chinese MMSE ranges from 0 to 30 points, with higher scores indicating better cognition. The CMMSE has been validated among the Chinese elderly population, and a score below 18 points has been defined as cognitive impairment [<xref ref-type="bibr" rid="ref24">24</xref>].</p>
        <p>Predictors related to cognitive impairment were assessed a priori based on clinical importance, scientific knowledge, and predictors identified in previously published studies [<xref ref-type="bibr" rid="ref25">25</xref>]. We therefore selected 45 factors related to demographic characteristics, which included lifestyle, mental health, leisure activities, sleep, chronic diseases, physical function, anthropometric index, and baseline cognitive function (<xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>).</p>
      </sec>
      <sec>
        <title>Statistical Analysis</title>
        <p>Categorical variables have been reported as numbers and proportions, and compared using a chi-square test or Fisher exact test. Continuous variables have been expressed as medians with IQRs and compared using the Wilcoxon test when data were not normally distributed. Detailed information is presented in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>. Some covariates contained missing values. The proportion of missing values was less than 5% for all variables. Thus, we performed imputations, using multivariable regression methods via the R package mice. Feature selection was performed using recursive feature elimination (RFE) combined with RF. During the process of elimination, a 10-fold cross-validation was implemented to optimize the variable selection. In addition, the RFE method with the NB method was used to extract variables, and the result was compared with RFE combined with RF. According to the results of RF and NB, the final feature selection was based on the number of features included and accuracy.</p>
        <p>We divided the original data into a 2/3 training set, 1/6 validation set, and 1/6 test set [<xref ref-type="bibr" rid="ref26">26</xref>]. The training set was used for model development. The validation set was used to adjust parameters of the model and explore optimal cutoffs after training was finished. The test set was used to estimate the generalization of the model. Regarding the algorithm used in the development of prediction models, we chose four machine learning algorithms, including RF, XGBoost, NB, and logistic regression, to construct models based on the results of the feature selection. We chose these four learning algorithms because they are recommended by “Guidelines for Developing and Reporting Machine Learning Predictive Models in Biomedical Research: A Multidisciplinary View” [<xref ref-type="bibr" rid="ref27">27</xref>]. The performances of the four prediction models were compared with each other using areas under the curve, specificity, sensitivity, accuracy, and specificity/sensitivity.</p>
        <p>In addition, if logistic regression performs well compared with the other three methods, we will formulate a nomogram based on the result of logistic regression for practical use. The nomogram works by proportionally converting each regression coefficient into a 0 to 100-point scale, with 100 points being the highest β coefficient. The points across each independent variable are added to derive total points, which are translated to predicted probabilities [<xref ref-type="bibr" rid="ref28">28</xref>]. All analyses were conducted using R, version 3.6.0 [<xref ref-type="bibr" rid="ref29">29</xref>]. A <italic>P</italic> value &#60;0.05 was considered to indicate statistical significance.</p>
      </sec>
    </sec>
    <sec sec-type="results">
      <title>Results</title>
      <sec>
        <title>Population Demographics</title>
        <p>A total of 6718 participants were involved. Forty-five explanatory variables were selected, and these variables included nine items of demographic characteristics, five items of lifestyle, 10 items of mental health, five items of leisure activities, two items of sleep, seven items of chronic diseases, two items of physical function, four items of the anthropometric index, and one item of baseline cognitive function. Six variables of demographic characteristics (age, sex, ethnicity, years of education, occupation, and marital status), four variables of lifestyle (fruit, smoking, drinking, and exercise), eight variables of mental health (self-reported quality of life, being positive, hygiene, anxiety, loneliness, decision making, feeling useless, and feeling happy), five variables of leisure activity (garden work, reading, raising pets, playing cards or mah-jongg, and social activities), two variables of sleep (sleep quality and sleep duration), five variables of chronic diseases (hypertension, diabetes, heart disease, cataract, and arthritis), two variables of physical function (activities of daily living and instrumental activities of daily living), one variable of anthropometric measurement (BMI), and baseline MMSE were significantly associated with a 3-year risk of cognitive impairment (<italic>P</italic>&#60;.001). Detailed information is presented in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>.</p>
      </sec>
      <sec>
        <title>Feature Selection</title>
        <p>NB combined with RFE showed that accuracy (0.8342) was the highest with four features included in the model (age, instrumental activities of daily living, baseline MMSE, and marital status). RF combined with RFE showed that the model involving 45 variables had the highest accuracy (0.8502), while the model including four variables had an accuracy of 0.8304 (<xref ref-type="table" rid="table1">Table 1</xref>). Considering the simplicity and accuracy of the prediction model, we finally chose the following four features to develop the model: age, instrumental activities of daily living, baseline MMSE, and marital status.</p>
        <table-wrap position="float" id="table1">
          <label>Table 1</label>
          <caption>
            <p>Feature selection using naïve Bayes combined with recursive feature elimination and random forest combined with recursive feature elimination.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="300"/>
            <col width="140"/>
            <col width="140"/>
            <col width="120"/>
            <col width="170"/>
            <col width="130"/>
            <thead>
              <tr valign="top">
                <td>Method</td>
                <td>Number of features</td>
                <td>Accuracy</td>
                <td>Kappa</td>
                <td>Accuracy SD</td>
                <td>Kappa SD</td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td>NB<sup>a</sup> combined with RFE<sup>b</sup></td>
                <td>4</td>
                <td>0.8342</td>
                <td>0.3258</td>
                <td>0.007801</td>
                <td>0.02452</td>
              </tr>
              <tr valign="top">
                <td>NB combined with RFE</td>
                <td>8</td>
                <td>0.8229</td>
                <td>0.3543</td>
                <td>0.007340</td>
                <td>0.02408</td>
              </tr>
              <tr valign="top">
                <td>NB combined with RFE</td>
                <td>16</td>
                <td>0.8136</td>
                <td>0.3421</td>
                <td>0.012724</td>
                <td>0.02540</td>
              </tr>
              <tr valign="top">
                <td>NB combined with RFE</td>
                <td>45</td>
                <td>0.8315</td>
                <td>0.3220</td>
                <td>0.007567</td>
                <td>0.02639</td>
              </tr>
              <tr valign="top">
                <td>RF<sup>c</sup> combined with RFE</td>
                <td>4</td>
                <td>0.8304</td>
                <td>0.1545</td>
                <td>0.008356</td>
                <td>0.05486</td>
              </tr>
              <tr valign="top">
                <td>RF combined with RFE</td>
                <td>8</td>
                <td>0.8475</td>
                <td>0.1594</td>
                <td>0.008545</td>
                <td>0.05569</td>
              </tr>
              <tr valign="top">
                <td>RF combined with RFE</td>
                <td>16</td>
                <td>0.8471</td>
                <td>0.1789</td>
                <td>0.007815</td>
                <td>0.03612</td>
              </tr>
              <tr valign="top">
                <td>RF combined with RFE</td>
                <td>45</td>
                <td>0.8502</td>
                <td>0.1214</td>
                <td>0.005572</td>
                <td>0.04800</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="table1fn1">
              <p><sup>a</sup>NB: naïve Bayes.</p>
            </fn>
            <fn id="table1fn2">
              <p><sup>b</sup>RFE: recursive feature elimination.</p>
            </fn>
            <fn id="table1fn3">
              <p><sup>c</sup>RF: random forest.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>Model Evaluation and Comparison</title>
        <p>The training, validation, and test sets involved 4514, 1100, and 1104 points of data, respectively. We tried to use several widely applied machine learning algorithms (RF, NB, XGBoost, and logistic regression) for the construction of the prediction models in the training set.</p>
        <p>We used a receiver operating characteristic (ROC) curve, specificity, sensitivity, accuracy, and specificity/sensitivity to evaluate the prediction model in both validation and test data. Before the evaluation, optimal cutoffs were determined by maximizing the Youden index (ie, sensitivity + specificity − 1) by the ROC curve in the validation set. In the test set, ROC curves revealed that logistic regression and NB had better predictive performances, with an area under the curve of 0.814. The area under the curve of XGBoost (0.811) was less than that of logistic regression and NB. RF underperformed, with an area under the curve of 0.780 (<xref rid="figure1" ref-type="fig">Figure 1</xref>).</p>
        <p>The model of NB performed well in terms of specificity, with a value of 0.776. The specificities of the models of logistic regression (0.770), RF (0.645), and XGBoost (0.738) were lower than that of NB. The model of RF performed well in terms of sensitivity, with a value of 0.793. The sensitivities of the models of logistic regression (0.701), NB (0.672), and XGBoost (0.724) were lower than that of RF. The accuracy of the NB model (0.760) was higher than the accuracies of the other three models. All details about the parameters of the models developed with different algorithms are shown in <xref ref-type="table" rid="table2">Table 2</xref>.</p>
        <fig id="figure1" position="float">
          <label>Figure 1</label>
          <caption>
            <p>Receiver operating characteristic curve performance of four models on the test set. AUC: area under the curve.</p>
          </caption>
          <graphic xlink:href="jmir_v23i2e20298_fig1.png" alt-version="no" mimetype="image" position="float" xlink:type="simple"/>
        </fig>
        <table-wrap position="float" id="table2">
          <label>Table 2</label>
          <caption>
            <p>Evaluation of the performance of the four algorithms.</p>
          </caption>
          <table width="1000" cellpadding="5" cellspacing="0" border="1" rules="groups" frame="hsides">
            <col width="180"/>
            <col width="130"/>
            <col width="70"/>
            <col width="100"/>
            <col width="120"/>
            <col width="120"/>
            <col width="120"/>
            <col width="160"/>
            <thead>
              <tr valign="top">
                <td>Algorithm</td>
                <td>Data set</td>
                <td>Area under the curve</td>
                <td>Optimal cutoff</td>
                <td>Specificity</td>
                <td>Sensitivity</td>
                <td>Accuracy</td>
                <td>Specificity/sensitivity</td>
              </tr>
            </thead>
            <tbody>
              <tr valign="top">
                <td>Logistic regression</td>
                <td>Validation</td>
                <td>0.812</td>
                <td>0.116</td>
                <td>0.785</td>
                <td>0.682</td>
                <td>0.768</td>
                <td>1.151</td>
              </tr>
              <tr valign="top">
                <td>Logistic regression</td>
                <td>Test</td>
                <td>0.814</td>
                <td>0.116</td>
                <td>0.770</td>
                <td>0.701</td>
                <td>0.759</td>
                <td>1.098</td>
              </tr>
              <tr valign="top">
                <td>Random forest</td>
                <td>Validation</td>
                <td>0.773</td>
                <td>0.040</td>
                <td>0.654</td>
                <td>0.784</td>
                <td>0.675</td>
                <td>0.834</td>
              </tr>
              <tr valign="top">
                <td>Random forest</td>
                <td>Test</td>
                <td>0.780</td>
                <td>0.040</td>
                <td>0.645</td>
                <td>0.793</td>
                <td>0.669</td>
                <td>0.813</td>
              </tr>
              <tr valign="top">
                <td>Naïve Bayes</td>
                <td>Validation</td>
                <td>0.804</td>
                <td>0.214</td>
                <td>0.796</td>
                <td>0.688</td>
                <td>0.778</td>
                <td>1.157</td>
              </tr>
              <tr valign="top">
                <td>Naïve Bayes</td>
                <td>Test</td>
                <td>0.814</td>
                <td>0.214</td>
                <td>0.776</td>
                <td>0.672</td>
                <td>0.760</td>
                <td>1.155</td>
              </tr>
              <tr valign="top">
                <td>XGBoost</td>
                <td>Validation</td>
                <td>0.815</td>
                <td>0.302</td>
                <td>0.753</td>
                <td>0.744</td>
                <td>0.752</td>
                <td>1.012</td>
              </tr>
              <tr valign="top">
                <td>XGBoost</td>
                <td>Test</td>
                <td>0.814</td>
                <td>0.302</td>
                <td>0.738</td>
                <td>0.724</td>
                <td>0.736</td>
                <td>1.019</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec>
        <title>Development of the Nomogram</title>
        <p>As the prediction developed by logistic regression performed well, a nomogram (<xref rid="figure2" ref-type="fig">Figure 2</xref>) was used to present the data and predicted probabilities vividly. The optimal cutoff value of the total nomogram scores was determined to be 170 in the test set. In <xref rid="figure2" ref-type="fig">Figure 2</xref>, a box has been used to represent the proportion of the sample in category variables. For instance, for marital status, most of the participants were grouped into “married or partnered” and “widowed.” Density exhibited the distribution of the sample in continuous variables. For example, for baseline MMSE, most individuals scored over 28. The total points corresponded to the predicted probability. For example, an individual score of 200 points in total, with an age score of 85, a marital status of widowed, an instrumental activities of daily living score of 6, and a baseline MMSE score of 22 corresponded to a predicted probability of cognitive impairment of 29.3%.</p>
        <fig id="figure2" position="float">
          <label>Figure 2</label>
          <caption>
            <p>Developed nomogram with age, marital status, instrumental activities of daily living (IADL), and baseline Mini-Mental State Examination (MMSE) incorporated.</p>
          </caption>
          <graphic xlink:href="jmir_v23i2e20298_fig2.png" alt-version="no" mimetype="image" position="float" xlink:type="simple"/>
        </fig>
      </sec>
    </sec>
    <sec sec-type="discussion">
      <title>Discussion</title>
      <sec>
        <title>Main Findings</title>
        <p>In this study, we developed a prediction model for forecasting the 3-year risk of cognitive impairment among 6718 community-dwelling elderly individuals aged 60 years or older with normal cognitive function via machine learning algorithms. The model performed comparably to the best available biomarkers, such as apolipoprotein genotype [<xref ref-type="bibr" rid="ref13">13</xref>,<xref ref-type="bibr" rid="ref17">17</xref>], but is less expensive, easier to implement, and validated internally with reasonable results.</p>
        <p>Feature or variable selection is central in the development of a prediction model [<xref ref-type="bibr" rid="ref30">30</xref>]. Out of the original 45 variables, the following four variables used showed the highest accuracy of the model: age, marital status, instrumental activities of daily living, and baseline MMSE. Our findings support the previous literature regarding age [<xref ref-type="bibr" rid="ref5">5</xref>,<xref ref-type="bibr" rid="ref31">31</xref>], marital status [<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref33">33</xref>], activities of daily living [<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref35">35</xref>], and cognitive status [<xref ref-type="bibr" rid="ref8">8</xref>,<xref ref-type="bibr" rid="ref36">36</xref>], indicating that the predictors we selected were usable and reliable.</p>
        <p>In this study, age was one of the predictors for the risk of cognitive impairment. It has already been estimated that, in 2020, 83% of people aged 75 years or above live with dementia in the US [<xref ref-type="bibr" rid="ref37">37</xref>]. Those aged 65 to 74 years account for 17% of cases, while those younger than 65 years could develop dementia, but it is much less common and the prevalence is uncertain [<xref ref-type="bibr" rid="ref37">37</xref>]. It is indicated that people aged 75 years or above should be screened for the risk of cognitive impairment. However, screening all older people for dementia is not recommended, as the benefits for that are still unclear [<xref ref-type="bibr" rid="ref5">5</xref>]. Using large existing registers and databases can offer opportunities to explore existing information to predict the health status [<xref ref-type="bibr" rid="ref38">38</xref>].</p>
        <p>We found that marital status was a strong predictor for the risk of cognitive impairment. A recent meta-analysis involving 812,047 participants evaluated the association between marriage and dementia. The results showed that life-long single and widowed older people were respectively 1.42 and 1.20 times more likely to be diagnosed with dementia compared with married older people [<xref ref-type="bibr" rid="ref33">33</xref>]. Another 10-year longitudinal population-based study including 2,288,489 individuals explored the influence of marital status and concluded that the risk of dementia in nonmarried individuals was around 1.7 times greater than that in married individuals [<xref ref-type="bibr" rid="ref32">32</xref>]. The results might be explained by the fact that married individuals are more likely to have healthy lifestyles and participate in social activities, which might be conducive to cognitive reserve and reduced dementia risk over a lifespan [<xref ref-type="bibr" rid="ref39">39</xref>]. On the contrary, those in widowhood might be more likely to experience a higher risk of cognitive impairment than divorced people because of the detrimental effect of stress from bereavement on hippocampal neurons or cognition. Further, as marriage has been considered a social norm, people with difficulties in communication and smaller cognitive reserves across life may be less likely to marry [<xref ref-type="bibr" rid="ref33">33</xref>]. In today’s society, staying unmarried has become more common, and this phenomenon deserves more attention. Social factors like marital status should be taken seriously as risk determinants for cognitive impairment.</p>
        <p>An association between physical function and cognitive capacity among older people has been found in previous studies [<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref40">40</xref>]. Our study only included instrumental activities of daily living as a predictor for constructing the model, and it did not consider activities of daily living that represent functional ability. The reason might be that there is a natural hierarchy of functional loss associated with cognitive decline among older people [<xref ref-type="bibr" rid="ref34">34</xref>]. Older persons with progressive cognitive decline lose the ability to perform tasks, often in the order of bathing, dressing, toileting, transferring, continence, and feeding. Therefore, older people who are not able to feed themselves might not be able to perform other tasks independently [<xref ref-type="bibr" rid="ref35">35</xref>]. Similarly, a study by Njegovan et al found that among the 14 items of activities of daily living and instrumental activities of daily living, a hierarchy of functional items existed, with instrumental activities of daily living (such as shopping, banking, etc) being lost at higher cognitive scores than basic activities of daily living (such as eating, dressing, etc), which were lost later [<xref ref-type="bibr" rid="ref34">34</xref>]. Our results confirmed that there was a tendency for instrumental activities of daily living to be a stronger predictor compared with activities of daily living. However, since there was overlap, subdomains of these two tools might be more meaningful for developing a prediction model. For nurses and caregivers, this information can help anticipate the need for intervention in people with declining cognition showing subtle declines in instrumental activities of daily living, which could improve the quality of life of these people and their caregivers and play an important part in health care planning [<xref ref-type="bibr" rid="ref34">34</xref>].</p>
        <p>Baseline cognitive function affected the degree to which cognitive scores changed over time and had a profound effect on further cognitive impairment. In one study using UK biobank data to assess the effect of baseline cognitive performance on a prediction model for 3 to 8-year risk of dementia, the results showed that cognitive performance added up to 5% (from 0.78 to 0.83) to the discriminative accuracy of the ROC model developed with the variables of age, sex, education, family history, and depression [<xref ref-type="bibr" rid="ref36">36</xref>]. The MMSE has been the most common cognitive variable for developing a dementia prediction model [<xref ref-type="bibr" rid="ref8">8</xref>]. However, variables of specific cognitive domains, such as memory and executive function, might be more feasible and useful predictors in constructing cognitive impairment prediction models. The total MMSE score was associated less strongly with dementia and Alzheimer disease than the episodic memory subset [<xref ref-type="bibr" rid="ref8">8</xref>]. Therefore, future studies could consider more specific cognitive domain variables.</p>
      </sec>
      <sec>
        <title>Limitations</title>
        <p>Our study has limitations, which should be considered in the interpretation of the study results. First, retained cohort members were younger and had on average better cognitive and physical functioning than those who dropped out, which can lead to studies being severely underpowered and biased toward the healthier part of the aging population. As we used a nationally representative database, the ascertainment bias could, to an extent, be limited. Second, we utilized a cross-validation approach to model development and assessment. The results still need to be validated in an independent cohort. Third, we used cohort studies with insufficient details on the duration of marriage, widowhood, and divorce to allow the exploration of a dose-response effect. A future study could take the dose-response effect of marital status on cognitive function into consideration. Fourth, the baseline MMSE was used as one of the predictors. However, other specific cognitive domains, such as memory and executive function, could also be used as features, and they might perform better than whole cognitive function. Fifth, our models were based on a prospective cohort that may have some level of bias. A prospective external validation cohort is needed for further confirmation in future research. Lastly, some predictors used in our study were measured by self-reporting, resulting in information bias. Nevertheless, self-reported data are more feasibly collected in primary health care settings, and the results can be generalized to wider communities. Despite these limitations, we believe that the results are usable in terms of cognitive impairment prevention and further intervention globally.</p>
      </sec>
      <sec>
        <title>Implications</title>
        <p>This is one of the first studies where a machine learning approach has been used in a nursing context. The study showed that machine learning can be used more widely in nursing science in different contexts and various functions. The prediction models exert implications in the three-grade prevention system of diseases [<xref ref-type="bibr" rid="ref38">38</xref>]. In the primary prevention of diseases, a cognitive impairment prediction model could provide quantitative risk value (probability) of cognitive deficiency in the next 3 years, based on the current health status, offering a more intuitive and powerful scientific tool for health education and behavioral intervention. In the secondary prevention of diseases, using noninvasive, low-cost, and easy-to-acquire variables to develop a prediction model is more practicable for staff, particularly general practitioners in community health, to bring about “early detection, early diagnosis, and early treatment,” which have large influences on medical costs for dementia. In the tertiary prevention of diseases, the prediction model could be used to predict recurrence, reducing mortality and disability [<xref ref-type="bibr" rid="ref38">38</xref>]. A simple and feasible prediction model would also help nurses to be aware of the progression of diseases over time. Therefore, nurses could be better aware of triggers that might alarm them about any hidden problems. In addition, a precise prediction model with predictors that are more available in clinical environments could help clinical nurses understand the prognostic factors of diseases. Based on this information, nurses could offer tailored preventive interventions to patients before any signs of cognition deficits occur.</p>
        <p>This study provides guidance for future research as well. First, the use of several algorithms to construct prediction models in specific diseases offers more opportunity to find a more suitable model with a high area under the curve and accuracy. Second, selecting the most suitable predictors is important for developing a prediction model to use in clinical practice. Easy-to-acquire, noninvasive, and low-cost variables are welcome in clinical nursing, and invasive biomarkers could improve the prediction. The former is more suitable for community health care and any clinical environment because of large populations and insufficient staff and funds, while the latter is more applicable in more specific clinical environments for people with high risk of diseases. Lastly, we included Chinese elderly people aged 60 years or above and developed a cognitive impairment prediction model. Further studies could develop cognitive impairment prediction models for middle-aged people as the World Health Organization has suggested to increase the cognitive reserve in mid-life and early aging (45-70 years) [<xref ref-type="bibr" rid="ref41">41</xref>].</p>
        <p>In the future, the results of this study could be used in countries and areas with less human resources, such as low- and middle-income countries, to identify elderly people with a high risk of developing cognitive deficiency in the next 3 years (ie, age, marital status, physical function, and cognitive function). Simple, relevant, and easy-to-detect risk factors would save time and resources in health care and would especially help nursing staff identify those people who are at high risk of developing cognitive impairment. As family members living with elderly people do not always recognize the early signs of dementia [<xref ref-type="bibr" rid="ref42">42</xref>], the knowledge obtained from this study could be used to educate family members as well.</p>
      </sec>
    </sec>
  </body>
  <back>
    <app-group>
      <supplementary-material id="app1">
        <label>Multimedia Appendix 1</label>
        <p>Flow chart of participant selection.</p>
        <media xlink:href="jmir_v23i2e20298_app1.docx" xlink:title="DOCX File , 25 KB"/>
      </supplementary-material>
      <supplementary-material id="app2">
        <label>Multimedia Appendix 2</label>
        <p>Detailed information about 45 features among the participants (grouped by cognitive impairment).</p>
        <media xlink:href="jmir_v23i2e20298_app2.docx" xlink:title="DOCX File , 35 KB"/>
      </supplementary-material>
    </app-group>
    <glossary>
      <title>Abbreviations</title>
      <def-list>
        <def-item>
          <term id="abb1">CLHLS</term>
          <def>
            <p>Chinese Longitudinal Healthy Longevity Survey</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb2">CMMSE</term>
          <def>
            <p>Chinese version of the Mini-Mental State Examination</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb3">MMSE</term>
          <def>
            <p>Mini-Mental State Examination</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb4">NB</term>
          <def>
            <p>naïve Bayes</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb5">RF</term>
          <def>
            <p>random forest</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb6">RFE</term>
          <def>
            <p>recursive feature elimination</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb7">ROC</term>
          <def>
            <p>receiver operating characteristic</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb8">TRIPOD</term>
          <def>
            <p>Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis</p>
          </def>
        </def-item>
      </def-list>
    </glossary>
    <ack>
      <p>We appreciate the support from the Special Funding for the Construction of Innovative Provinces in Hunan (grant number: 2019SK2141), China Scholarship Council (grant number: Liumeijin 2020-1509), and Central South University-Flinders University Seed Project (grant number: 2020xyhlzzjj002).</p>
    </ack>
    <fn-group>
      <fn fn-type="con">
        <p>MYH and XYW conceived of the presented idea. MYH and XHS performed the analytical calculations and took the lead in writing the manuscript. GY verified the analytical methods. VM investigated and supervised the findings of this work and helped in the language edit. HF supervised the whole project. In addition, VM and HF contributed equally to this manuscript.</p>
      </fn>
      <fn fn-type="conflict">
        <p>None declared.</p>
      </fn>
    </fn-group>
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