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Authordc.contributor.authorSilva Contreras, Sebastián Jesús 
Authordc.contributor.authorMedina Ortiz, David 
Authordc.contributor.authorConca Rosende, Carlos 
Authordc.contributor.authorOlivera Nappa, Álvaro 
Admission datedc.date.accessioned2020-05-15T14:27:18Z
Available datedc.date.available2020-05-15T14:27:18Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationFront. Bioeng. Biotechnol. March 2020 | Volume 8 | Article 195es_ES
Identifierdc.identifier.other10.3389/fbioe.2020.00195
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/174746
Abstractdc.description.abstractExisting mathematical models for the glucose-insulin (G-I) dynamics often involve variables that are not susceptible to direct measurement. Standard clinical tests for measuring G-I levels for diagnosing potential diseases are simple and relatively cheap, but seldom give enough information to allow the identification of model parameters within the range in which they have a biological meaning, thus generating a gap between mathematical modeling and any possible physiological explanation or clinical interpretation. In the present work, we present a synthetic mathematical model to represent the G-I dynamics in an Oral Glucose Tolerance Test (OGTT), which involves for the first time for OGTT-related models, Delay Differential Equations. Our model can represent the radically different behaviors observed in a studied cohort of 407 normoglycemic patients (the largest analyzed so far in parameter fitting experiments), all masked under the current threshold-based normality criteria. We also propose a novel approach to solve the parameter fitting inverse problem, involving the clustering of different G-I profiles, a simulation-based exploration of the feasible set, and the construction of an information function which reshapes it, based on the clinical records, experimental uncertainties, and physiological criteria. This method allowed an individual-wise recognition of the parameters of our model using small size OGTT data (5 measurements) directly, without modifying the routine procedures or requiring particular clinical setups. Therefore, our methodology can be easily applied to gain parametric insights to complement the existing tools for the diagnosis of G-I dysregulations. We tested the parameter stability and sensitivity for individual subjects, and an empirical relationship between such indexes and curve shapes was spotted. Since different G-I profiles, under the light of our model, are related to different physiological mechanisms, the present method offers a tool for personally-oriented diagnosis and treatment and to better define new health criteria.es_ES
Patrocinadordc.description.sponsorshipCentre for Biotechnology and Bioengineering - CeBiB (PIA project, Conicyt, Chile): FB0001. Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT): 21181435. supercomputing infrastructure of the National Laboratory for High-Performance Computing, NLHPC, Chile: ECM-02.es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherFrontiers Mediaes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceFrontiers in Bioengineering and Biotechnologyes_ES
Keywordsdc.subjectMathematical modelinges_ES
Keywordsdc.subjectGlucose-insulin controles_ES
Keywordsdc.subjectOGTTes_ES
Keywordsdc.subjectInverse problemses_ES
Keywordsdc.subjectPersonalized medicinees_ES
Títulodc.titleA novel synthetic model of the glucose-insulin system for patient-wise inference of physiological parameters from small-size OGTT dataes_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorrvhes_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile