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dc.contributor.authorLoizou, Christos P.en
dc.contributor.authorPetroudi, Stylianien
dc.contributor.authorSeimenis, Ioannisen
dc.contributor.authorPantzaris, Marios C.en
dc.contributor.authorPattichis, Constantinos S.en
dc.creatorLoizou, Christos P.en
dc.creatorPetroudi, Stylianien
dc.creatorSeimenis, Ioannisen
dc.creatorPantzaris, Marios C.en
dc.creatorPattichis, Constantinos S.en
dc.date.accessioned2019-11-13T10:41:07Z
dc.date.available2019-11-13T10:41:07Z
dc.date.issued2015
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/54453
dc.description.abstractIntroduction: This study investigates the application of texture analysis methods on brain T2-white matter lesions detected with magnetic resonance imaging (MRI) for the prognosis of future disability in subjects diagnosed with clinical isolated syndrome (CIS) of multiple sclerosis (MS). Methods: Brain lesions and normal appearing white matter (NAWM) from 38 symptomatic untreated subjects diagnosed with CIS as well as normal white matter (NWM) from 20 healthy volunteers, were manually segmented, by an experienced MS neurologist, on transverse T2-weighted images obtained from serial brain MR imaging scans (0 and 6-12 months). Additional clinical information in the form of the Expanded Disability Status Scale (EDSS), a scale from 0 to 10, which provides a way of quantifying disability in MS and monitoring the changes over time in the level of disability, were also provided. Shape and most importantly different texture features including GLCM and laws were then extracted for all above regions, after image intensity normalization. Results: The findings showed that: (i) there were significant differences for the texture futures extracted between the NAWM and lesions at 0 month and between NAWM and lesions at 6-12. months. However, no significant differences were found for all texture features extracted when comparing lesions temporally at 0 and 6-12. months with the exception of contrast (gray level difference statistics-GLDS) and difference entropy (spatial gray level dependence matrix-SGLDM)en
dc.description.abstract(ii) significant differences were found between NWM and NAWM for most of the texture features investigated in this studyen
dc.description.abstract(iii) there were significant differences found for the lesion texture features at 0 month for those with EDSS. ≤. 2 versus those with EDSS. >. 2 (mean, median, inverse difference moment and sum average) and for the lesion texture features at 6-12. months with EDSS. >. 2 and EDSS. ≤. 2 for the texture features (mean, median, entropy and sum average). It should be noted that whilst there were no differences in entropy at time 0 between the two groups, significant change was observed at 6-12. months, relating the corresponding features to the follow-up and disability (EDSS) progression. For the NAWM, significant differences were found between 0 month and 6-12 months with EDSS. ≤. 2 (contrast, inverse difference moment), for 6-12. months for EDSS. >. 2 and 0 month with EDSS. >. 2 (difference entropy) and for 6-12 months for EDSS. >. 2 and EDSS. ≤. 2 (sum average)en
dc.description.abstract(iv) there was no significant difference for NAWM and the lesion texture features (for both 0 and 6-12. months) for subjects with no change in EDSS score versus subjects with increased EDSS score from 2 to 5. years. Conclusions: The findings of this study provide evidence that texture features of T2 MRI brain white matter lesions may have an additional potential role in the clinical evaluation of MRI images in MS and perhaps may provide some prognostic evidence in relation to future disability of patients. However, a larger scale study is needed to establish the application in clinical practice and for computing shape and texture features that may provide information for better and earlier differentiation between normal brain tissue and MS lesions. © 2014 Elsevier Masson SAS.en
dc.sourceJournal of Neuroradiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84926420902&doi=10.1016%2fj.neurad.2014.05.006&partnerID=40&md5=5234784f94cca41d2de5cd6d49da286d
dc.subjectAlgorithmsen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectadulten
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectalgorithmen
dc.subjectprognosisen
dc.subjectquantitative analysisen
dc.subjectclinical articleen
dc.subjectclinical practiceen
dc.subjectmaleen
dc.subjectMultiple sclerosisen
dc.subjectReproducibility of Resultsen
dc.subjectproceduresen
dc.subjectpathologyen
dc.subjectnuclear magnetic resonance imagingen
dc.subjectArticleen
dc.subjectclinical evaluationen
dc.subjectsensitivity and specificityen
dc.subjectscoring systemen
dc.subjectimage analysisen
dc.subjectreproducibilityen
dc.subjectMRIen
dc.subjectneuroimagingen
dc.subjectwhite matteren
dc.subjectthree dimensional imagingen
dc.subjectdemyelinating diseaseen
dc.subjectautomated pattern recognitionen
dc.subjectPattern Recognition, Automateden
dc.subjectentropyen
dc.subjectImaging, Three-Dimensionalen
dc.subjectdisabilityen
dc.subjectTexture analysisen
dc.subjectcomputer assisted diagnosisen
dc.subjectimage enhancementen
dc.subjectImage Interpretation, Computer-Assisteden
dc.subjectShape featuresen
dc.subjectDemyelinating Diseasesen
dc.subjectdiffusion tensor imagingen
dc.subjectEDSSen
dc.subjectExpanded Disability Status Scaleen
dc.subjectneurologisten
dc.subjecttexture feature analysisen
dc.subjectwhite matter lesionen
dc.titleQuantitative texture analysis of brain white matter lesions derived from T2-weighted MR images in MS patients with clinically isolated syndromeen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.neurad.2014.05.006
dc.description.volume42
dc.description.issue2
dc.description.startingpage99
dc.description.endingpage114
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Πληροφορικής / Department of Computer Science
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :8</p>en
dc.source.abbreviationJ.Neuroradiol.en
dc.contributor.orcidPattichis, Constantinos S. [0000-0003-1271-8151]
dc.contributor.orcidLoizou, Christos P. [0000-0003-1247-8573]
dc.contributor.orcidPantzaris, Marios C. [0000-0003-2937-384X]
dc.gnosis.orcid0000-0003-1271-8151
dc.gnosis.orcid0000-0003-1247-8573
dc.gnosis.orcid0000-0003-2937-384X


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