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dc.contributor.author
Sartoretti, Elisabeth
dc.contributor.author
Sartoretti, Thomas
dc.contributor.author
Wyss, Michael
dc.contributor.author
Becker, Anton S.
dc.contributor.author
Schwenk, Arpad
dc.contributor.author
Van Smoorenburg, Luuk
dc.contributor.author
Najafi, Arash
dc.contributor.author
Binkert, Christoph
dc.contributor.author
Thoeny, Harriet C.
dc.contributor.author
Zhou, Jinyuan
dc.contributor.author
Jiang, Shanshan
dc.contributor.author
Graf, Nicole
dc.contributor.author
Czell, David
dc.contributor.author
Sartoretti-Schefer, Sabine
dc.contributor.author
Reischauer, Carolin
dc.date.accessioned
2020-02-25T09:03:19Z
dc.date.available
2020-01-07T04:54:24Z
dc.date.available
2020-01-07T09:01:45Z
dc.date.available
2020-02-25T09:03:19Z
dc.date.issued
2019-12
dc.identifier.issn
1664-2295
dc.identifier.other
10.3389/fneur.2019.01307
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/387872
dc.identifier.doi
10.3929/ethz-b-000387872
dc.description.abstract
Objectives: To assess the ability of 3D amide proton transfer weighted (APTw) imaging based on magnetization transfer analysis to discriminate between multiple sclerosis lesions (MSL) and white matter hyperintensities of presumed vascular origin (WMH) and to compare APTw signal intensity of healthy white matter (healthy WM) with APTw signal intensity of MSL and WHM. Materials and Methods: A total of 27 patients (16 female, 11 males, mean age 39.6 years) with multiple sclerosis, 35 patients (17 females, 18 males, mean age 66.6 years) with small vessel disease (SVD) and 20 healthy young volunteers (9 females, 11 males, mean age 29 years) were included in the MSL, the WMH, and the healthy WM group. MSL and WMH were segmented on fluid attenuated inversion recovery (FLAIR) images underlaid onto APTw images. Histogram parameters (mean, median, 10th, 25th, 75th, 90th percentile) were calculated. Mean APTw signal intensity values in healthy WM were defined by “Region of interest” (ROI) measurements. Wilcoxon rank sum tests and receiver operating characteristics (ROC) curve analyses of clustered data were applied. Results: All histogram parameters except the 75 and 90th percentile were significantly different between MSL and WMH (p = 0.018–p = 0.034). MSL presented with higher median values in all parameters. The histogram parameters offered only low diagnostic performance in discriminating between MSL and WMH. The 10th percentile yielded the highest diagnostic performance with an AUC of 0.6245 (95% CI: [0.532, 0.717]). Mean APTw signal intensity values of MSL were significantly higher than mean values of healthy WM (p = 0.005). The mean values of WMH did not differ significantly from the values of healthy WM (p = 0.345). Conclusions: We found significant differences in APTw signal intensity, based on straightforward magnetization transfer analysis, between MSL and WMH and between MSL and healthy WM. Low AUC values from ROC analyses, however, suggest that it may be challenging to determine type of lesion with APTw imaging. More advanced analysis of the APT CEST signal may be helpful for further differentiation of MSL and WMH.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Frontiers Media
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
magnetic resonance imaging
en_US
dc.subject
amide proton transfer
en_US
dc.subject
molecular imaging
en_US
dc.subject
multiple sclerosis lesions
en_US
dc.subject
white matter lesions
en_US
dc.subject
CEST
en_US
dc.title
Amide Proton Transfer Weighted Imaging Shows Differences in Multiple Sclerosis Lesions and White Matter Hyperintensities of Presumed Vascular Origin
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2019-12-10
ethz.journal.title
Frontiers in Neurology
ethz.journal.volume
10
en_US
ethz.journal.abbreviated
Front. Neurol.
ethz.pages.start
1307
en_US
ethz.size
11 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Lausanne
ethz.publication.status
published
en_US
ethz.date.deposited
2020-01-07T04:54:28Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2020-01-07T09:01:56Z
ethz.rosetta.lastUpdated
2024-02-02T10:29:06Z
ethz.rosetta.versionExported
true
ethz.COinS
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