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dc.contributor.authorIglesias, Juan Eugenio
dc.contributor.authorVan Leemput, Koen
dc.contributor.authorAugustinackc, Jean
dc.contributor.authorInsausti, Ricardo
dc.contributor.authorFischl, Bruce
dc.contributor.authorReuter, Martin
dc.date.accessioned2017-03-08T12:15:53Z
dc.date.available2017-03-08T12:15:53Z
dc.date.issued2016
dc.identifier.citationJuan Eugenio Iglesias, Koen Van Leemput, Jean Augustinack, Ricardo Insausti, Bruce Fischl, Martin Reuter, Bayesian longitudinal segmentation of hippocampal substructures in brain MRI using subject-specific atlases, NeuroImage, Volume 141, 1 November 2016, Pages 542-555, ISSN 1053-8119, http://dx.doi.org/10.1016/j.neuroimage.2016.07.020.es
dc.identifier.issn1053-8119
dc.identifier.urihttp://hdl.handle.net/10810/20880
dc.descriptionOnline publication 15/07/2016es
dc.description.abstractThe hippocampal formation is a complex, heterogeneous structure that consists of a number of distinct, interacting subregions. Atrophy of these subregions is implied in a variety of neurodegenerative diseases, most prominently in Alzheimer’s disease (AD). Thanks to the increasing resolution ofMRimages and computational atlases, automatic segmentation of hippocampal subregions is becoming feasible in MRI scans. Here we introduce a generative model for dedicated longitudinal segmentation that relies on subject-specific atlases. The segmentations of the scans at the different time points are jointly computed using Bayesian inference. All time points are treated the same to avoid processing bias. We evaluate this approach using over 4700 scans from two publicly available datasets (ADNI and MIRIAD). In test–retest reliability experiments, the proposed method yielded significantly lower volume differences and significantly higher Dice overlaps than the cross-sectional approach for nearly every subregion (average across subregions: 4.5% vs. 6.5%, Dice overlap: 81.8% vs. 75.4%). The longitudinal algorithm also demonstrated increased sensitivity to group differences: in MIRIAD (69 subjects: 46 with AD and 23 controls), it found differences in atrophy rates between AD and controls that the cross sectional method could not detect in a number of subregions: right parasubiculum, left and right presubiculum, right subiculum, left dentate gyrus, left CA4, left HATA and right tail. In ADNI (836 subjects: 369 with AD, 215 with early cognitive impairment — eMCI — and 252 controls), all methods found significant differences between AD and controls, but the proposed longitudinal algorithm detected differences between controls and eMCI and differences between eMCI and AD that the cross sectional method could not find: left presubiculum, right subiculum, left and right parasubiculum, left and right HATA. Moreover, many of the differences that the cross-sectional method already found were detected with higher significance. The presented algorithm will be made available as part of the open-source neuroimaging package FreeSurfer.es
dc.description.sponsorshipThis project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No.654911 (project “THALAMODEL”), and also from the Spanish Ministry of Economy and Competitiveness (MINECO, reference TEC2014-51882-P). Support for this research was also provided in part by the National Cancer Institute (1K25-CA181632-01), the Genentech Foundation (G-40819) and the Nvidia corporation, which donated a Titan X GPU. Further support was provided by the A.A. Martinos Center for Biomedical Imaging (P41RR014075, P41EB015896, U24RR021382), and was made possible by the resources provided by Shared Instrumentation Grants1S10RR023401, 1S10RR019307, and 1S10RR023043. Support was also provided by the National Institute for Biomedical Imaging and Bioengineering (R01EB006758, R21EB018907, R01EB019956), the National Institute on Aging (5R01AG008122, R01AG016495), the National Institute for Neurological Disorders and Stroke (R01NS0525851, R21NS072652, R01NS070963, R01NS083534, 5U01NS086625) and the Lundbeck Foundation (R141-2013-13117), Additional support was provided by the NIH Blueprint for Neuroscience Research (5U01-MH093765), as part of the multi-institutional Human Connectome Project. In addition, BF has a financial interest in CorticoMetrics, a company whose medical pursuits focus on brain imaging and measurement technologies. BF's interests were reviewed and are managed by Massachusetts General Hospital and Partners HealthCare in accordance with their conflict of interest policies. The collection and sharing of the MRI data used in the group study based on ADNI was funded by the Alzheimer's Disease Neuroimaging Initiative (National Institutes of Health Grant U01 AG024904) and DOD ADNI (U.S. Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: Alzheimer's Association; Alzheimer's Drug Discovery Foundation; BioClinica, Inc.; Biogen Idec Inc.; Bristol-Myers Squibb Company; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; GE Healthcare; Innogenetics, N.V.; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Medpace, Inc.; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Synarc Inc.; and Takeda Pharmaceutical Company. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer's Disease Cooperative Study at the University of California, San Diego. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.es
dc.language.isoenges
dc.publisherNeuroImagees
dc.relationinfo:eu-repo/grantAgreement/MINECO/TEC2014-51882-P
dc.relationinfo:eu-repo/grantAgreement/EC/MARIE-CURIE-654911
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectHippocampal subfieldses
dc.subjectLongitudinal modelinges
dc.subjectSegmentationes
dc.subjectBayesian modelinges
dc.titleBayesian longitudinal segmentation of hippocampal substructures in brain MRI using subject-specific atlaseses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2016 The Authors. Published by Elsevier Inc.This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).es
dc.relation.publisherversionhttps://www.journals.elsevier.com/neuroimagees
dc.identifier.doi10.1016/j.neuroimage.2016.07.020
dc.subject.categoriaCOGNITIVE NEUROSCIENCE
dc.subject.categoriaNEUROLOGY


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