Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0181624
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dc.titleDiffusion tensor imaging profiles reveal specific neural tract distortion in normal pressure hydrocephalus
dc.contributor.authorKeong N.C.
dc.contributor.authorPena A.
dc.contributor.authorPrice S.J.
dc.contributor.authorCzosnyka M.
dc.contributor.authorCzosnyka Z.
dc.contributor.authorDevito E.E.
dc.contributor.authorHousden C.R.
dc.contributor.authorSahakian B.J.
dc.contributor.authorPickard J.D.
dc.date.accessioned2019-11-01T07:49:55Z
dc.date.available2019-11-01T07:49:55Z
dc.date.issued2017
dc.identifier.citationKeong N.C., Pena A., Price S.J., Czosnyka M., Czosnyka Z., Devito E.E., Housden C.R., Sahakian B.J., Pickard J.D. (2017). Diffusion tensor imaging profiles reveal specific neural tract distortion in normal pressure hydrocephalus. PLoS ONE 12 (8) : e0181624. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0181624
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161179
dc.description.abstractBackground The pathogenesis of normal pressure hydrocephalus (NPH) remains unclear which limits both early diagnosis and prognostication. The responsiveness to intervention of differing, complex and concurrent injury patterns on imaging have not been well-characterized. We used diffusion tensor imaging (DTI) to explore the topography and reversibility of white matter injury in NPH pre- and early after shunting. Methods Twenty-five participants (sixteen NPH patients and nine healthy controls) underwent DTI, pre-operatively and at two weeks post-intervention in patients. We interrogated 40 datasets to generate a full panel of DTI measures and corroborated findings with plots of isotropy (p) vs. anisotropy (q). Results Concurrent examination of DTI measures revealed distinct profiles for NPH patients vs. controls. PQ plots demonstrated that patterns of injury occupied discrete white matter districts. DTI profiles for different white matter tracts showed changes consistent with i) predominant transependymal diffusion with stretch/ compression, ii) oedema with or without stretch/ compression and iii) predominant stretch/ compression. Findings were specific to individual tracts and dependent upon their proximity to the ventricles. At two weeks post-intervention, there was a 67% drop in axial diffusivity (p = 0022) in the posterior limb of the internal capsule, compatible with improvement in stretch/ compression, that preceded any discernible changes in clinical outcome. On PQ plots, the trajectories of the posterior limb of the internal capsule and inferior longitudinal fasciculus suggested attempted ‘round trips’. i.e. return to normality. Conclusion DTI profiling with p:q correlation may offer a non-invasive biomarker of the characteristics of potentially reversible white matter injury. © 2017 Keong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectaged
dc.subjectcase control study
dc.subjectdiffusion tensor imaging
dc.subjectfemale
dc.subjecthuman
dc.subjectHydrocephalus, Normal Pressure
dc.subjectimage processing
dc.subjectmale
dc.subjectmiddle aged
dc.subjectnerve tract
dc.subjectneuropsychological test
dc.subjectpathology
dc.subjectprocedures
dc.subjectvery elderly
dc.subjectwhite matter
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectCase-Control Studies
dc.subjectDiffusion Tensor Imaging
dc.subjectFemale
dc.subjectHumans
dc.subjectHydrocephalus, Normal Pressure
dc.subjectImage Processing, Computer-Assisted
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeural Pathways
dc.subjectNeuropsychological Tests
dc.subjectWhite Matter
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1371/journal.pone.0181624
dc.description.sourcetitlePLoS ONE
dc.description.volume12
dc.description.issue8
dc.description.pagee0181624
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