Outcome Prediction in Mathematical Models of Immune Response to Infection
Clinicians need to predict patient outcomes with high accuracy as early as possible after disease inception. In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to i...
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description | Clinicians need to predict patient outcomes with high accuracy as early as possible after disease inception. In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to infection. However, accuracy can be increased at the expense of delayed prognosis. We investigate several systems of ordinary differential equations (ODEs) that model the host immune response to a pathogen load. Advantages of systems of ODEs for investigating the immune response to infection include the ability to collect data on large numbers of 'virtual patients', each with a given set of model parameters, and obtain many time points during the course of the infection. We implement patient-to-patient variability v in the ODE models by randomly selecting the model parameters from distributions with coefficients of variation v that are centered on physiological values. We use logistic regression with one-versus-all classification to predict the discrete steady-state outcomes of the system. We find that the prediction algorithm achieves near 100% accuracy for v = 0, and the accuracy decreases with increasing v for all ODE models studied. The fact that multiple steady-state outcomes can be obtained for a given initial condition, i.e. the basins of attraction overlap in the space of initial conditions, limits the prediction accuracy for v > 0. Increasing the elapsed time of the variables used to train and test the classifier, increases the prediction accuracy, while adding explicit external noise to the ODE models decreases the prediction accuracy. Our results quantify the competition between early prognosis and high prediction accuracy that is frequently encountered by clinicians. |
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In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to infection. However, accuracy can be increased at the expense of delayed prognosis. We investigate several systems of ordinary differential equations (ODEs) that model the host immune response to a pathogen load. Advantages of systems of ODEs for investigating the immune response to infection include the ability to collect data on large numbers of 'virtual patients', each with a given set of model parameters, and obtain many time points during the course of the infection. We implement patient-to-patient variability v in the ODE models by randomly selecting the model parameters from distributions with coefficients of variation v that are centered on physiological values. We use logistic regression with one-versus-all classification to predict the discrete steady-state outcomes of the system. We find that the prediction algorithm achieves near 100% accuracy for v = 0, and the accuracy decreases with increasing v for all ODE models studied. The fact that multiple steady-state outcomes can be obtained for a given initial condition, i.e. the basins of attraction overlap in the space of initial conditions, limits the prediction accuracy for v > 0. Increasing the elapsed time of the variables used to train and test the classifier, increases the prediction accuracy, while adding explicit external noise to the ODE models decreases the prediction accuracy. Our results quantify the competition between early prognosis and high prediction accuracy that is frequently encountered by clinicians.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0135861</identifier><identifier>PMID: 26287609</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Accuracy ; Algorithms ; Analysis ; Artificial intelligence ; Bacterial Infections - immunology ; Basins ; Classification ; Clinical outcomes ; Coefficient of variation ; Differential equations ; Genomes ; Humans ; Immune response ; Immune system ; Infection ; Infections ; Infectious diseases ; Inflammation ; Influenza ; Initial conditions ; Mathematical models ; Mechanical engineering ; Medical prognosis ; Model accuracy ; Models, Biological ; Models, Theoretical ; Nonlinear Dynamics ; Ordinary differential equations ; Outcome Assessment (Health Care) - methods ; Parameters ; Patient outcomes ; Patients ; Physics ; Physiological aspects ; Prognosis ; Science ; Steady state ; Systems Biology - methods ; Tuberculosis ; Variability ; Virus Diseases - immunology</subject><ispartof>PloS one, 2015-08, Vol.10 (8), p.e0135861-e0135861</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Mai et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Mai et al 2015 Mai et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-c2a607e0886093844b5dd168a16dec80606c0619bb6c96ff1b6ca3db542d83673</citedby><cites>FETCH-LOGICAL-c692t-c2a607e0886093844b5dd168a16dec80606c0619bb6c96ff1b6ca3db542d83673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545748/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545748/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23864,27922,27923,53789,53791,79370,79371</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26287609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Yates, Andrew J.</contributor><creatorcontrib>Mai, Manuel</creatorcontrib><creatorcontrib>Wang, Kun</creatorcontrib><creatorcontrib>Huber, Greg</creatorcontrib><creatorcontrib>Kirby, Michael</creatorcontrib><creatorcontrib>Shattuck, Mark D</creatorcontrib><creatorcontrib>O'Hern, Corey S</creatorcontrib><title>Outcome Prediction in Mathematical Models of Immune Response to Infection</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Clinicians need to predict patient outcomes with high accuracy as early as possible after disease inception. In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to infection. However, accuracy can be increased at the expense of delayed prognosis. We investigate several systems of ordinary differential equations (ODEs) that model the host immune response to a pathogen load. Advantages of systems of ODEs for investigating the immune response to infection include the ability to collect data on large numbers of 'virtual patients', each with a given set of model parameters, and obtain many time points during the course of the infection. We implement patient-to-patient variability v in the ODE models by randomly selecting the model parameters from distributions with coefficients of variation v that are centered on physiological values. We use logistic regression with one-versus-all classification to predict the discrete steady-state outcomes of the system. 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Our results quantify the competition between early prognosis and high prediction accuracy that is frequently encountered by clinicians.</description><subject>Accuracy</subject><subject>Algorithms</subject><subject>Analysis</subject><subject>Artificial intelligence</subject><subject>Bacterial Infections - immunology</subject><subject>Basins</subject><subject>Classification</subject><subject>Clinical outcomes</subject><subject>Coefficient of variation</subject><subject>Differential equations</subject><subject>Genomes</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Infection</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Inflammation</subject><subject>Influenza</subject><subject>Initial conditions</subject><subject>Mathematical models</subject><subject>Mechanical engineering</subject><subject>Medical prognosis</subject><subject>Model accuracy</subject><subject>Models, Biological</subject><subject>Models, Theoretical</subject><subject>Nonlinear Dynamics</subject><subject>Ordinary differential equations</subject><subject>Outcome Assessment (Health Care) - methods</subject><subject>Parameters</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Physics</subject><subject>Physiological aspects</subject><subject>Prognosis</subject><subject>Science</subject><subject>Steady state</subject><subject>Systems Biology - methods</subject><subject>Tuberculosis</subject><subject>Variability</subject><subject>Virus Diseases - immunology</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkktr3DAUhU1padK0_6C0hkJpFzPVy5K8KYTQhyFhSvrYClmSZzTI1tSSS_LvK884YVyyKF7IXH_nXN-rk2UvIVhCzOCHrR_6TrrlzndmCSAuOIWPslNYYrSgCODHR-8n2bMQtgAUmFP6NDtBFHFGQXmaVashKt-a_FtvtFXR-i63XX4l48a0MlolXX7ltXEh901ete3QmfzahNQ1mDz6vOoas5c9z5400gXzYjrPsp-fP_24-Lq4XH2pLs4vF4qWKC4UkhQwAzhP_TEnpC60hpRLSLVRHFBAFaCwrGuqSto0MJ0S67ogSHNMGT7LXh98d84HMW0hCMgALxFhHCeiOhDay63Y9baV_a3w0op9wfdrIfs0mjOCaiYxYZAizUitFEdA8qaQRZ3KEo1eH6duQ90arUwXe-lmpvMvnd2Itf8jSEEKRngyeDcZ9P73YEIUrQ3KOCc744f9fxcMQwJH9M0_6MPTTdRapgFs1_jUV42m4pyki0WclDRRyweo9GjTWpUi09hUnwnezwSJieYmruUQgqi-X_8_u_o1Z98esRsjXdwE74YxMmEOkgOoeh9Cb5r7JUMgxsTfbUOMiRdT4pPs1fEF3YvuIo7_At1W-c8</recordid><startdate>20150819</startdate><enddate>20150819</enddate><creator>Mai, Manuel</creator><creator>Wang, Kun</creator><creator>Huber, Greg</creator><creator>Kirby, Michael</creator><creator>Shattuck, Mark D</creator><creator>O'Hern, Corey S</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150819</creationdate><title>Outcome Prediction in Mathematical Models of Immune Response to Infection</title><author>Mai, Manuel ; Wang, Kun ; Huber, Greg ; Kirby, Michael ; Shattuck, Mark D ; O'Hern, Corey S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-c2a607e0886093844b5dd168a16dec80606c0619bb6c96ff1b6ca3db542d83673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Accuracy</topic><topic>Algorithms</topic><topic>Analysis</topic><topic>Artificial intelligence</topic><topic>Bacterial Infections - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mai, Manuel</au><au>Wang, Kun</au><au>Huber, Greg</au><au>Kirby, Michael</au><au>Shattuck, Mark D</au><au>O'Hern, Corey S</au><au>Yates, Andrew J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcome Prediction in Mathematical Models of Immune Response to Infection</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-08-19</date><risdate>2015</risdate><volume>10</volume><issue>8</issue><spage>e0135861</spage><epage>e0135861</epage><pages>e0135861-e0135861</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Clinicians need to predict patient outcomes with high accuracy as early as possible after disease inception. In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to infection. However, accuracy can be increased at the expense of delayed prognosis. We investigate several systems of ordinary differential equations (ODEs) that model the host immune response to a pathogen load. Advantages of systems of ODEs for investigating the immune response to infection include the ability to collect data on large numbers of 'virtual patients', each with a given set of model parameters, and obtain many time points during the course of the infection. We implement patient-to-patient variability v in the ODE models by randomly selecting the model parameters from distributions with coefficients of variation v that are centered on physiological values. We use logistic regression with one-versus-all classification to predict the discrete steady-state outcomes of the system. We find that the prediction algorithm achieves near 100% accuracy for v = 0, and the accuracy decreases with increasing v for all ODE models studied. The fact that multiple steady-state outcomes can be obtained for a given initial condition, i.e. the basins of attraction overlap in the space of initial conditions, limits the prediction accuracy for v > 0. Increasing the elapsed time of the variables used to train and test the classifier, increases the prediction accuracy, while adding explicit external noise to the ODE models decreases the prediction accuracy. Our results quantify the competition between early prognosis and high prediction accuracy that is frequently encountered by clinicians.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26287609</pmid><doi>10.1371/journal.pone.0135861</doi><tpages>e0135861</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Accuracy Algorithms Analysis Artificial intelligence Bacterial Infections - immunology Basins Classification Clinical outcomes Coefficient of variation Differential equations Genomes Humans Immune response Immune system Infection Infections Infectious diseases Inflammation Influenza Initial conditions Mathematical models Mechanical engineering Medical prognosis Model accuracy Models, Biological Models, Theoretical Nonlinear Dynamics Ordinary differential equations Outcome Assessment (Health Care) - methods Parameters Patient outcomes Patients Physics Physiological aspects Prognosis Science Steady state Systems Biology - methods Tuberculosis Variability Virus Diseases - immunology |
title | Outcome Prediction in Mathematical Models of Immune Response to Infection |
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