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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/math10081221</dc:identifier><dc:language>eng</dc:language><dc:creator>Aznar-Gimeno, Rocío</dc:creator><dc:creator>Esteban, Luis M.</dc:creator><dc:creator>Hoyo-Alonso, Rafael del</dc:creator><dc:creator>Borque-Fernando, Ángel</dc:creator><dc:creator>Sanz, Gerardo</dc:creator><dc:title>A stepwise algorithm for linearly combining biomakers under Youden Index maximisation</dc:title><dc:identifier>ART-2022-128017</dc:identifier><dc:description>Combining multiple biomarkers to provide predictive models with a greater discriminatory ability is a discipline that has received attention in recent years. Choosing the probability threshold that corresponds to the highest combined marker accuracy is key in disease diagnosis. The Youden index is a statistical metric that provides an appropriate synthetic index for diagnostic accuracy and a good criterion for choosing a cut-off point to dichotomize a biomarker. In this study, we present a new stepwise algorithm for linearly combining continuous biomarkers to maximize the Youden index. To investigate the performance of our algorithm, we analyzed a wide range of simulated scenarios and compared its performance with that of five other linear combination methods in the literature (a stepwise approach introduced by Yin and Tian, the min-max approach, logistic regression, a parametric approach under multivariate normality and a non-parametric kernel smoothing approach). The obtained results show that our proposed stepwise approach showed similar results to other algorithms in normal simulated scenarios and outperforms all other algorithms in non-normal simulated scenarios. In scenarios of biomarkers with the same means and a different covariance matrix for the diseased and non-diseased population, the min-max approach outperforms the rest. The methods were also applied on two real datasets (to discriminate Duchenne muscular dystrophy and prostate cancer), whose results also showed a higher predictive ability in our algorithm in the prostate cancer database</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/112091</dc:source><dc:doi>10.3390/math10081221</dc:doi><dc:identifier>http://zaguan.unizar.es/record/112091</dc:identifier><dc:identifier>oai:zaguan.unizar.es:112091</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E46-20R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/T17-20R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2020-116873GB-I00</dc:relation><dc:identifier.citation>Mathematics 10, 8 (2022), 1221 [26 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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