Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance

Background: Hypointense lesions on T1-weighted images have important clinical relevance in multiple sclerosis patients. Traditionally, spin-echo (SE) sequences are used to assess these lesions (termed black holes), but Fast Spoiled Gradient-Echo (FSPGR) sequences provide an excellent alternative.Obj...

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Main Authors: Krisztián Kocsis, Nikoletta Szabó, Eszter Tóth, András Király, Péter Faragó, Bálint Kincses, Dániel Veréb, Bence Bozsik, Katalin Boross, Melinda Katona, Péter Bodnár, Nyúl Gábor László, László Vécsei, Péter Klivényi, Krisztina Bencsik, Zsigmond Tamás Kincses
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.619135/full
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author Krisztián Kocsis
Nikoletta Szabó
Eszter Tóth
András Király
Péter Faragó
Bálint Kincses
Dániel Veréb
Bence Bozsik
Katalin Boross
Melinda Katona
Péter Bodnár
Nyúl Gábor László
László Vécsei
László Vécsei
Péter Klivényi
Krisztina Bencsik
Zsigmond Tamás Kincses
Zsigmond Tamás Kincses
author_facet Krisztián Kocsis
Nikoletta Szabó
Eszter Tóth
András Király
Péter Faragó
Bálint Kincses
Dániel Veréb
Bence Bozsik
Katalin Boross
Melinda Katona
Péter Bodnár
Nyúl Gábor László
László Vécsei
László Vécsei
Péter Klivényi
Krisztina Bencsik
Zsigmond Tamás Kincses
Zsigmond Tamás Kincses
author_sort Krisztián Kocsis
collection DOAJ
description Background: Hypointense lesions on T1-weighted images have important clinical relevance in multiple sclerosis patients. Traditionally, spin-echo (SE) sequences are used to assess these lesions (termed black holes), but Fast Spoiled Gradient-Echo (FSPGR) sequences provide an excellent alternative.Objective: To determine whether the contrast difference between T1 hypointense lesions and the surrounding normal white matter is similar on the two sequences, whether different lesion types could be identified, and whether the clinical relevance of these lesions types are different.Methods: Seventy-nine multiple sclerosis patients' lesions were manually segmented, then registered to T1 sequences. Median intensity values of lesions were identified on all sequences, then K-means clustering was applied to assess whether distinct clusters of lesions can be defined based on intensity values on SE, FSPGR, and FLAIR sequences. The standardized intensity of the lesions in each cluster was compared to the intensity of the normal appearing white matter in order to see if lesions stand out from the white matter on a given sequence.Results: 100% of lesions on FSPGR images and 69% on SE sequence in cluster #1 exceeded a standardized lesion distance of Z = 2.3 (p < 0.05). In cluster #2, 78.7% of lesions on FSPGR and only 17.7% of lesions on SE sequence were above this cutoff value, meaning that these lesions were not easily seen on SE images. Lesion count in the second cluster (lesions less identifiable on SE) significantly correlated with the Expanded Disability Status Scale (EDSS) (R: 0.30, p ≤ 0.006) and with disease duration (R: 0.33, p ≤ 0.002).Conclusion: We showed that black holes can be separated into two distinct clusters based on their intensity values on various sequences, only one of which is related to clinical parameters. This emphasizes the joint role of FSPGR and SE sequences in the monitoring of MS patients and provides insight into the role of black holes in MS.
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spelling doaj.art-79a3c51b641c485c831700cfd1c994d82022-12-21T20:17:23ZengFrontiers Media S.A.Frontiers in Neurology1664-22952021-03-011210.3389/fneur.2021.619135619135Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical RelevanceKrisztián Kocsis0Nikoletta Szabó1Eszter Tóth2András Király3Péter Faragó4Bálint Kincses5Dániel Veréb6Bence Bozsik7Katalin Boross8Melinda Katona9Péter Bodnár10Nyúl Gábor László11László Vécsei12László Vécsei13Péter Klivényi14Krisztina Bencsik15Zsigmond Tamás Kincses16Zsigmond Tamás Kincses17Department of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Radiology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Image Processing and Computer Graphics, University of Szeged, Szeged, HungaryDepartment of Image Processing and Computer Graphics, University of Szeged, Szeged, HungaryDepartment of Image Processing and Computer Graphics, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryMagyar Tudományos Akadémia-Szegedi Tudományegyetem (MTA-SZTE) Neuroscience Research Group, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Neurology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryDepartment of Radiology, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, HungaryBackground: Hypointense lesions on T1-weighted images have important clinical relevance in multiple sclerosis patients. Traditionally, spin-echo (SE) sequences are used to assess these lesions (termed black holes), but Fast Spoiled Gradient-Echo (FSPGR) sequences provide an excellent alternative.Objective: To determine whether the contrast difference between T1 hypointense lesions and the surrounding normal white matter is similar on the two sequences, whether different lesion types could be identified, and whether the clinical relevance of these lesions types are different.Methods: Seventy-nine multiple sclerosis patients' lesions were manually segmented, then registered to T1 sequences. Median intensity values of lesions were identified on all sequences, then K-means clustering was applied to assess whether distinct clusters of lesions can be defined based on intensity values on SE, FSPGR, and FLAIR sequences. The standardized intensity of the lesions in each cluster was compared to the intensity of the normal appearing white matter in order to see if lesions stand out from the white matter on a given sequence.Results: 100% of lesions on FSPGR images and 69% on SE sequence in cluster #1 exceeded a standardized lesion distance of Z = 2.3 (p < 0.05). In cluster #2, 78.7% of lesions on FSPGR and only 17.7% of lesions on SE sequence were above this cutoff value, meaning that these lesions were not easily seen on SE images. Lesion count in the second cluster (lesions less identifiable on SE) significantly correlated with the Expanded Disability Status Scale (EDSS) (R: 0.30, p ≤ 0.006) and with disease duration (R: 0.33, p ≤ 0.002).Conclusion: We showed that black holes can be separated into two distinct clusters based on their intensity values on various sequences, only one of which is related to clinical parameters. This emphasizes the joint role of FSPGR and SE sequences in the monitoring of MS patients and provides insight into the role of black holes in MS.https://www.frontiersin.org/articles/10.3389/fneur.2021.619135/fullmultiple sclerosisT1 hypointense lesionsblack holesMRI protocolclusteringclinical state
spellingShingle Krisztián Kocsis
Nikoletta Szabó
Eszter Tóth
András Király
Péter Faragó
Bálint Kincses
Dániel Veréb
Bence Bozsik
Katalin Boross
Melinda Katona
Péter Bodnár
Nyúl Gábor László
László Vécsei
László Vécsei
Péter Klivényi
Krisztina Bencsik
Zsigmond Tamás Kincses
Zsigmond Tamás Kincses
Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
Frontiers in Neurology
multiple sclerosis
T1 hypointense lesions
black holes
MRI protocol
clustering
clinical state
title Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
title_full Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
title_fullStr Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
title_full_unstemmed Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
title_short Two Classes of T1 Hypointense Lesions in Multiple Sclerosis With Different Clinical Relevance
title_sort two classes of t1 hypointense lesions in multiple sclerosis with different clinical relevance
topic multiple sclerosis
T1 hypointense lesions
black holes
MRI protocol
clustering
clinical state
url https://www.frontiersin.org/articles/10.3389/fneur.2021.619135/full
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