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dc.creatorSchmidt-Richberg, Alexanderes
dc.creatorGuerrero, Ricardoes
dc.creatorLedig, Christianes
dc.creatorMolina Abril, Helenaes
dc.creatorFrangi, Alejandro F.es
dc.creatorRueckert, Danieles
dc.date.accessioned2020-02-26T11:01:58Z
dc.date.available2020-02-26T11:01:58Z
dc.date.issued2015
dc.identifier.citationSchmidt-Richberg, A., Guerrero, R., Ledig, C., Molina Abril, H., Frangi, A.F. y Rueckert, D. (2015). Multi-stage Biomarker Models for Progression Estimation in Alzheimer’s Disease. En IPMI 2015: 24th International Conference on Information Processing in Medical Imaging (387-398), Sabhal Mor Ostaig, Isle of Skye, UK: Springer.
dc.identifier.isbn978-3-319-19991-7es
dc.identifier.issn0302-9743es
dc.identifier.urihttps://hdl.handle.net/11441/93658
dc.description.abstractThe estimation of disease progression in Alzheimer’s disease (AD) based on a vector of quantitative biomarkers is of high interest to clinicians, patients, and biomedical researchers alike. In this work, quantile regression is employed to learn statistical models describing the evolution of such biomarkers. Two separate models are constructed using (1) subjects that progress from a cognitively normal (CN) stage to mild cognitive impairment (MCI) and (2) subjects that progress from MCI to AD during the observation window of a longitudinal study. These models are then automatically combined to develop a multi-stage disease progression model for the whole disease course. A probabilistic approach is derived to estimate the current disease progress (DP) and the disease progression rate (DPR) of a given individual by fitting any acquired biomarkers to these models. A particular strength of this method is that it is applicable even if individual biomarker measurements are missing for the subject. Employing cognitive scores and image-based biomarkers, the presented method is used to estimate DP and DPR for subjects from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Further, the potential use of these values as features for different classification tasks is demonstrated. For example, accuracy of 64% is reached for CN vs. MCI vs. AD classification.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherSpringeres
dc.relation.ispartofIPMI 2015: 24th International Conference on Information Processing in Medical Imaging (2015), p 387-398
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleMulti-stage Biomarker Models for Progression Estimation in Alzheimer’s Diseasees
dc.typeinfo:eu-repo/semantics/conferenceObjectes
dc.type.versioninfo:eu-repo/semantics/submittedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Matemática Aplicada I (ETSII)es
dc.relation.publisherversionhttps://link.springer.com/chapter/10.1007%2F978-3-319-19992-4_30es
dc.identifier.doi10.1007/978-3-319-19992-4_30es
idus.format.extent12es
dc.publication.initialPage387es
dc.publication.endPage398es
dc.eventtitleIPMI 2015: 24th International Conference on Information Processing in Medical Imaginges
dc.eventinstitutionSabhal Mor Ostaig, Isle of Skye, UKes
dc.relation.publicationplaceCham, Switzerlandes

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