Enhanced multiple sclerosis diagnosis using high-resolution 3D OCT volumes with synthetic slices

UDC.coleccionInvestigaciónes_ES
UDC.departamentoCiencias da Computación e Tecnoloxías da Informaciónes_ES
UDC.endPage105es_ES
UDC.grupoInvGrupo de Visión Artificial e Recoñecemento de Patróns (VARPA)es_ES
UDC.institutoCentroCITIC - Centro de Investigación de Tecnoloxías da Información e da Comunicaciónes_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.journalTitlePattern Recognition Letterses_ES
UDC.startPage99es_ES
UDC.volume189es_ES
dc.contributor.authorLópez-Varela, Emilio
dc.contributor.authorOlivier Pascual, Nuria
dc.contributor.authorQuezada-Sánchez, Johnny
dc.contributor.authorOreja-Guevara, Celia
dc.contributor.authorSantos Bueso, Enrique
dc.contributor.authorBarreira, Noelia
dc.date.accessioned2025-05-09T14:36:22Z
dc.date.available2025-05-09T14:36:22Z
dc.date.issued2025-03
dc.description.abstract[Abstract]: Optical Coherence Tomography (OCT), known for its micron-level resolution and non-invasive nature, is essential in diagnosing Multiple Sclerosis (MS). Accurate MS diagnosis through OCT is facilitated by identifying changes in retinal layer thickness, which serve as biomarkers, such as the retinal nerve fiber layer and the macular ganglion cell layer. To adequately diagnose MS, it is crucial to detect thickness changes in specific small regions of the retina, necessitating extensive retinal coverage with minimal granularity. However, a significant challenge in using OCT for MS diagnosis is the inverse relationship between the number of slices and the image quality of OCT volumes. High-resolution images require longer acquisition times, which limits the number of slices that can be obtained and results in covering a smaller area of the retina. Conversely, increasing the number of slices reduces individual image quality, impairing the detection of retinal layer structures. To address this issue, we propose a novel approach for the automatic detection of MS using high-resolution synthetic 3D OCT volumes. Our methodology involves using a generative network to synthesize intermediate slices, thereby enhancing retinal coverage without degrading image quality. This synthetic augmentation improves cross-sectional resolution, providing more comprehensive retinal details. Then we use a segmentation network to extract biomarkers and multiple 3D classification models to directly detect MS automatically. Our results demonstrate significant improvements in accuracy and reliability. Integrating synthetic slices into OCT volumes enhances the detection of MS, underscoring the potential of generative models for better clinical outcomes in MS diagnosis.es_ES
dc.description.sponsorshipXunta de Galicia; ED431C 2020/24es_ES
dc.description.sponsorshipXunta de Galicia; ED431G 2019/01es_ES
dc.description.sponsorshipThis research was funded by Government of Spain, Ministerio de Ciencia e Innovación y Universidades, Government of Spain, RTI2018- 095894-B-I00 research project; Ministerio de Ciencia e Innovación, Government of Spain through the research projects with reference PID2019-108435RB-I00, reference PDC2022-133132-I00 and TED2021-131201B-I00; Consellería de Cultura, Educación e Universi- dade, Xunta de Galicia through the Grupos de Referencia Competitiva, grant ref. ED431C 2020/24; CITIC, as Research Center accredited by Galician University System, is funded by ‘‘Consellería de Cultura, Educación e Universidade from Xunta de Galicia’’, supported in an 80% through ERDF Funds, ERDF Operational Programme Galicia 2014– 2020, and the remaining 20% by ‘‘Secretaría Xeral de Universidades’’, grant ref. ED431G 2019/01. Emilio López Varela acknowledges its support under FPI Grant Program through PID2019-108435RB-I00 project.es_ES
dc.identifier.citationLópez-Varela, E., Pascual, N. O., Quezada-Sánchez, J., Oreja-Guevara, C., Bueso, E. S., & Barreira, N. (2025). Enhanced multiple sclerosis diagnosis using high-resolution 3D OCT volumes with synthetic slices. Pattern Recognition Letters, v.189, pp 99-105. https://doi.org/10.1016/j.patrec.2025.01.011es_ES
dc.identifier.doi10.1016/j.patrec.2025.01.011
dc.identifier.issn0167-8655
dc.identifier.issn1872-7344
dc.identifier.urihttp://hdl.handle.net/2183/41956
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-095894-B-I00/ES/DESARROLLO DE TECNOLOGIAS INTELIGENTES PARA DIAGNOSTICO DE LA DMAE BASADAS EN EL ANALISIS AUTOMATICO DE NUEVAS MODALIDADES HETEROGENEAS DE ADQUISICION DE IMAGEN OFTALMOLOGICAes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108435RB-I00/ES/CUANTIFICACION Y CARACTERIZACION COMPUTACIONAL DE IMAGEN MULTIMODAL OFTALMOLOGICA: ESTUDIOS EN ESCLEROSIS MULTIPLEes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2024/PDC2022-133132-I00/ES/MEJORAS EN EL DIAGNÓSTICO E INVESTIGACIÓN CLÍNICO MEDIANTE TECNOLOGÍAS INTELIGENTES APLICADAS LA IMAGEN OFTALMOLÓGICAes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2024/TED2021-131201B-I00/ES/DIAGNÓSTICO DIGITAL: TRANSFORMACIÓN DE LA DETECCIÓN DE ENFERMEDADES NEUROVASCULARES Y DEL TRATAMIENTO DE LOS PACIENTESes_ES
dc.relation.urihttps://doi.org/10.1016/j.patrec.2025.01.011es_ES
dc.rightsAtribución 4.0 Internacionales_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectMedical synthesises_ES
dc.subjectClassificationes_ES
dc.subjectMultiple sclerosises_ES
dc.subjectOptical coherence tomographyes_ES
dc.subjectSynthesises_ES
dc.titleEnhanced multiple sclerosis diagnosis using high-resolution 3D OCT volumes with synthetic sliceses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication04d0827c-a1f6-4be1-bd1e-b97a583a5540
relation.isAuthorOfPublication39c18658-f8b9-44c2-866a-ef7e53839489
relation.isAuthorOfPublication.latestForDiscovery04d0827c-a1f6-4be1-bd1e-b97a583a5540

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