3D shape analysis of the brain's third ventricle using a midplane encoded symmetric template model

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dc.contributor.authorKim, Jaeilko
dc.contributor.authorHernandez, Maria del C. Valdesko
dc.contributor.authorRoyle, Natalie Ako
dc.contributor.authorManiega, Susana Munozko
dc.contributor.authorAribisala, Benjamin Sko
dc.contributor.authorGow, Alan Jko
dc.contributor.authorBastin, Mark Eko
dc.contributor.authorDeary, Ian Jko
dc.contributor.authorWardlaw, Joanna Mko
dc.contributor.authorPark, Jinahko
dc.date.accessioned2016-07-05T07:49:36Z-
dc.date.available2016-07-05T07:49:36Z-
dc.date.created2016-02-24-
dc.date.created2016-02-24-
dc.date.issued2016-06-
dc.identifier.citationCOMPUTER METHODS AND PROGRAMS IN BIOMEDICINE, v.129, pp.51 - 62-
dc.identifier.issn0169-2607-
dc.identifier.urihttp://hdl.handle.net/10203/209202-
dc.description.abstractBackground: Structural changes of the brain's third ventricle have been acknowledged as an indicative measure of the brain atrophy progression in neurodegenerative and endocrinal diseases. To investigate the ventricular enlargement in relation to the atrophy of the surrounding structures, shape analysis is a promising approach. However, there are hurdles in modeling the third ventricle shape. First, it has topological variations across individuals due to the inter-thalamic adhesion. In addition, as an interhemispheric structure, it needs to be aligned to the midsagittal plane to assess its asymmetric and regional deformation. Method: To address these issues, we propose a model-based shape assessment. Our template model of the third ventricle consists of a midplane and a symmetric mesh of generic shape. By mapping the template's midplane to the individuals' brain midsagittal plane, we align the symmetric mesh on the midline of the brain before quantifying the third ventricle shape. To build the vertex-wise correspondence between the individual third ventricle and the template mesh, we employ a minimal-distortion surface deformation framework. In addition, to account for topological variations, we implement geometric constraints guiding the template mesh to have zero width where the inter-thalamic adhesion passes through, preventing vertices crossing between left and right walls of the third ventricle. The individual shapes are compared using a vertex-wise deformity from the symmetric template. Results: Experiments on imaging and demographic data from a study of aging showed that our model was sensitive in assessing morphological differences between individuals in relation to brain volume (i.e. proxy for general brain atrophy), gender and the fluid intelligence at age 72. It also revealed that the proposed method can detect the regional and asymmetrical deformation unlike the conventional measures: volume (median 1.95 ml, IQR 0.96 ml) and width of the third ventricle. Similarity measures between binary masks and the shape model showed that the latter reconstructed shape details with high accuracy (Dice coefficient >= 0.9, mean distance 0.5 mm and Hausdorff distance 2.7 mm). Conclusions: We have demonstrated that our approach is suitable to morphometrical analyses of the third ventricle, providing high accuracy and inter-subject consistency in the shape quantification. This shape modeling method with geometric constraints based on anatomical landmarks could be extended to other brain structures which require a consistent measurement basis in the morphometry. (C) 2016 The Authors. Published by Elsevier Ireland Ltd.-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectBIRTH COHORT 1936-
dc.subjectMULTIPLE-SCLEROSIS-
dc.subjectATROPHY-
dc.subjectSCHIZOPHRENIA-
dc.subjectREGISTRATION-
dc.subjectAGE-
dc.subjectOPTIMIZATION-
dc.subjectHIPPOCAMPUS-
dc.subjectCOGNITION-
dc.subjectDISEASE-
dc.title3D shape analysis of the brain's third ventricle using a midplane encoded symmetric template model-
dc.typeArticle-
dc.identifier.wosid000374839000007-
dc.identifier.scopusid2-s2.0-84960909490-
dc.type.rimsART-
dc.citation.volume129-
dc.citation.beginningpage51-
dc.citation.endingpage62-
dc.citation.publicationnameCOMPUTER METHODS AND PROGRAMS IN BIOMEDICINE-
dc.identifier.doi10.1016/j.cmpb.2016.02.014-
dc.contributor.localauthorPark, Jinah-
dc.contributor.nonIdAuthorHernandez, Maria del C. Valdes-
dc.contributor.nonIdAuthorRoyle, Natalie A-
dc.contributor.nonIdAuthorManiega, Susana Munoz-
dc.contributor.nonIdAuthorAribisala, Benjamin S-
dc.contributor.nonIdAuthorGow, Alan J-
dc.contributor.nonIdAuthorBastin, Mark E-
dc.contributor.nonIdAuthorDeary, Ian J-
dc.contributor.nonIdAuthorWardlaw, Joanna M-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorBrain-
dc.subject.keywordAuthorThird ventricle-
dc.subject.keywordAuthorShape analysis-
dc.subject.keywordAuthor3D model-
dc.subject.keywordAuthorAging-
dc.subject.keywordAuthorAtrophy-
dc.subject.keywordPlusBIRTH COHORT 1936-
dc.subject.keywordPlusMULTIPLE-SCLEROSIS-
dc.subject.keywordPlusATROPHY-
dc.subject.keywordPlusSCHIZOPHRENIA-
dc.subject.keywordPlusREGISTRATION-
dc.subject.keywordPlusAGE-
dc.subject.keywordPlusOPTIMIZATION-
dc.subject.keywordPlusHIPPOCAMPUS-
dc.subject.keywordPlusCOGNITION-
dc.subject.keywordPlusDISEASE-
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