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Brain and Ventricle Volume Alterations in Idiopathic Normal Pressure Hydrocephalus Determined by Artificial Intelligence-Based MRI Volumetry

dc.contributor.authorBendella, Zeynep
dc.contributor.authorPurrer, Veronika
dc.contributor.authorHaase, Robert
dc.contributor.authorZülow, Stefan
dc.contributor.authorKindler, Christine
dc.contributor.authorBorger, Valerie
dc.contributor.authorBanat, Mohammed
dc.contributor.authorDorn, Franziska
dc.contributor.authorWüllner, Ullrich
dc.contributor.authorRadbruch, Alexander
dc.contributor.authorSchmeel, Frederic Carsten
dc.date.accessioned2025-08-06T15:49:52Z
dc.date.available2025-08-06T15:49:52Z
dc.date.issued03.07.2024
dc.identifier.urihttps://hdl.handle.net/20.500.11811/13317
dc.description.abstractThe aim of this study was to employ artificial intelligence (AI)-based magnetic resonance imaging (MRI) brain volumetry to potentially distinguish between idiopathic normal pressure hydrocephalus (iNPH), Alzheimer's disease (AD), and age- and sex-matched healthy controls (CG) by evaluating cortical, subcortical, and ventricular volumes. Additionally, correlations between the measured brain and ventricle volumes and two established semi-quantitative radiologic markers for iNPH were examined. An IRB-approved retrospective analysis was conducted on 123 age- and sex-matched subjects (41 iNPH, 41 AD, and 41 controls), with all of the iNPH patients undergoing routine clinical brain MRI prior to ventriculoperitoneal shunt implantation. Automated AI-based determination of different cortical and subcortical brain and ventricular volumes in mL, as well as calculation of population-based normalized percentiles according to an embedded database, was performed; the CE-certified software mdbrain v4.4.1 or above was used with a standardized T1-weighted 3D magnetization-prepared rapid gradient echo (MPRAGE) sequence. Measured brain volumes and percentiles were analyzed for between-group differences and correlated with semi-quantitative measurements of the Evans' index and corpus callosal angle: iNPH patients exhibited ventricular enlargement and changes in gray and white matter compared to AD patients and controls, with the most significant differences observed in total ventricular volume (+67%) and the lateral (+68%), third (+38%), and fourth (+31%) ventricles compared to controls. Global ventriculomegaly and marked white matter reduction with concomitant preservation of gray matter compared to AD and CG were characteristic of iNPH, whereas global and frontoparietally accentuated gray matter reductions were characteristic of AD. Evans' index and corpus callosal angle differed significantly between the three groups and moderately correlated with the lateral ventricular volumes in iNPH patients [Evans' index (r > 0.83, p ≤ 0.001), corpus callosal angle (r < −0.74, p ≤ 0.001)]. AI-based MRI volumetry in iNPH patients revealed global ventricular enlargement and focal brain atrophy, which, in contrast to healthy controls and AD patients, primarily involved the supratentorial white matter and was marked temporomesially and in the midbrain, while largely preserving gray matter. Integrating AI volumetry in conjunction with traditional radiologic measures could enhance iNPH identification and differentiation, potentially improving patient management and therapy response assessment.en
dc.format.extent23
dc.language.isoeng
dc.rightsNamensnennung 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectnormal pressure hydrocephalus
dc.subjectbrain atrophy
dc.subjectquantitative neuroimaging
dc.subjectautomated volumetrization
dc.subject.ddc610 Medizin, Gesundheit
dc.titleBrain and Ventricle Volume Alterations in Idiopathic Normal Pressure Hydrocephalus Determined by Artificial Intelligence-Based MRI Volumetry
dc.typeWissenschaftlicher Artikel
dc.publisher.nameMDPI
dc.publisher.locationBasel
dc.rights.accessRightsopenAccess
dcterms.bibliographicCitation.volume2024, vol. 14
dcterms.bibliographicCitation.issueiss. 13, 1422
dcterms.bibliographicCitation.pagestart1
dcterms.bibliographicCitation.pageend23
dc.relation.doihttps://doi.org/10.3390/diagnostics14131422
dcterms.bibliographicCitation.journaltitleDiagnostics
ulbbn.pubtypeZweitveröffentlichung
dc.versionpublishedVersion
ulbbn.sponsorship.oaUnifundOA-Förderung Universität Bonn


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Namensnennung 4.0 International