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Biomechanics of human optic chiasmal compression: ex vivo experiment and finite element modelling

dc.contributor.authorWang, Xiaofei
dc.contributor.authorNeely, Andrew
dc.contributor.authorJain, Neeranjali
dc.contributor.authorJain, Swaranjali
dc.contributor.authorJain, Sanjiv
dc.contributor.authorTahtali, Murat
dc.contributor.authorMcIlwaine, Gawn G.
dc.contributor.authorLueck, Christian
dc.date.accessioned2023-07-18T23:57:13Z
dc.date.available2023-07-18T23:57:13Z
dc.date.issued2022
dc.date.updated2022-05-15T08:16:54Z
dc.description.abstractThe mechanism of bitemporal hemianopia arising as a result of chiasmal compression is unknown. In this study, we combined an ex vivo experiment and finite element modelling (FEM) to investigate its potential mechanism. A cadaveric human optic chiasm was scanned using micro-CT before and after deformation by inflation of Foley catheter, to simulate tumour growth from beneath. The geometry of the same chiasm was reconstructed and simulated using finite element analysis. Chiasmal deformations were extracted from the simulation and compared with those observed during micro-CT scanning. In addition, nerve fibre models examining variation in local fibre distribution patterns of the chiasm were incorporated to investigate the strain (deformation) distributions of the chiasm at an axonal level. The FEM model matched the micro-CT scans well both qualitatively and quantitatively. Compression of the chiasm induced high strains in the paracentral portions of the chiasm where the crossing optic nerve fibres are located. At an axonal level, the magnitude of strains affecting crossed fibres were greater than those affecting uncrossed fibres. The high strains in the paracentral portions of the chiasm, combined with the differences in strain between crossed and uncrossed nerve fibres, are consistent with a biomechanical explanation for the pattern of visual field loss seen in chiasmal compression.en_AU
dc.description.sponsorshipSupported by National Natural Science Foundation of China (12002025).en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn2590-0935en_AU
dc.identifier.urihttp://hdl.handle.net/1885/294392
dc.language.isoen_AUen_AU
dc.provenanceThis is an open access article under the CCBY-NC-ND license(http://creativecommons.org/licenses/by nc-nd/4.0/)en_AU
dc.publisherElsevier BVen_AU
dc.rights© 2021 The authorsen_AU
dc.rights.licenseCreative Commons Attribution licenceen_AU
dc.rights.urihttp://creativecommons.org/licenses/ by-nc-nd/4.0/en_AU
dc.sourceMedicine in Novel Technology and Devicesen_AU
dc.subjectBitemporal hemianopiaen_AU
dc.subjectPituitary tumouren_AU
dc.subjectChiasmen_AU
dc.subjectFinite element modellingen_AU
dc.subjectOptic nerve fibreen_AU
dc.titleBiomechanics of human optic chiasmal compression: ex vivo experiment and finite element modellingen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.lastpage8en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationWang, Xiaofei, University of new South Walesen_AU
local.contributor.affiliationNeely, Andrew, University of New South Walesen_AU
local.contributor.affiliationJain, Neeranjali, Department of Neurology, The Canberra Hospital, Canberraen_AU
local.contributor.affiliationJain, Swaranjali, The Canberra Hospitalen_AU
local.contributor.affiliationJain, Sanjiv, Canberra Hospitalen_AU
local.contributor.affiliationTahtali, Murat, University of New South Walesen_AU
local.contributor.affiliationMcIlwaine, Gawn G., Queen's University, Belfasten_AU
local.contributor.affiliationLueck, Christian, College of Health and Medicine, ANUen_AU
local.contributor.authoruidLueck, Christian, u1807496en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor321201 - Ophthalmologyen_AU
local.identifier.absfor320903 - Central nervous systemen_AU
local.identifier.absfor320904 - Computational neuroscience (incl. mathematical neuroscience and theoretical neuroscience)en_AU
local.identifier.absseo200101 - Diagnosis of human diseases and conditionsen_AU
local.identifier.ariespublicationa383154xPUB26053en_AU
local.identifier.citationvolume13en_AU
local.identifier.doi10.1016/j.medntd.2021.100113en_AU
local.identifier.scopusID2-s2.0-85122957763
local.publisher.urlhttps://www.sciencedirect.com/en_AU
local.type.statusPublished Versionen_AU

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