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dc.contributor.authorEgnell, Liv Elisabet
dc.contributor.authorVidic, Igor
dc.contributor.authorJerome, Neil Peter
dc.contributor.authorBofin, Anna M.
dc.contributor.authorBathen, Tone Frost
dc.contributor.authorGoa, Pål Erik
dc.date.accessioned2020-03-11T08:09:09Z
dc.date.available2020-03-11T08:09:09Z
dc.date.created2020-01-13T13:57:39Z
dc.date.issued2019
dc.identifier.citationJournal of Magnetic Resonance Imaging. 2019, 1-11.nb_NO
dc.identifier.issn1053-1807
dc.identifier.urihttp://hdl.handle.net/11250/2646309
dc.description.abstractBackground:Increased deposition and reorientation of stromal collagenfibers are associated with breast cancer progres-sion and invasiveness. Diffusion-weighted imaging (DWI) may be sensitive to the collagenfiber organization in the stromaand could provide important biomarkers for breast cancer characterization.Purpose:To understand how collagenfibers influence water diffusion in vivo and evaluate the relationship between colla-gen content and the apparent diffusion coefficient (ADC) and the signal fractions of the biexponential model using a highb-value scheme.Study Type:Prospective.Subjects/Specimens:Forty-five patients with benign (n= 8), malignant (n= 36), and ductal carcinoma in situ (n= 1) breasttumors. Lesions and normalfibroglandular tissue (n= 9) were analyzed using sections of formalin-fixed, paraffin-embeddedtissue stained with hematoxylin, erythrosine, and saffron.Field Strength/Sequence:MRI (3T) protocols:Protocol I:Twice-refocused spin-echo echo-planar imaging with: echo time(TE) 85 msec; repetition time (TR) 9300/11600 msec; matrix 90×90×60; voxel size 2×2×2.5 mm3;b-values: 0 and700 s/mm2.Protocol II:Stejskal–Tanner spin-echo echo-planar imaging with: TE: 88 msec; TR: 10600/11800 msec, matrix90×90×60; voxel size 2×2×2.5 mm3;b-values [0, 200, 600, 1200, 1800, 2400, 3000] s/mm2.Assessment:Area fractions of cellular and collagen content in histologic sections were quantified using whole-slide imageanalysis and compared with the corresponding DWI parameters.Statistical Tests:Correlations were assessed using Pearson’sr. Univariate analysis of group median values was done usingthe Mann–WhitneyU-test.Results:Collagen content correlated with the fast signal fraction (r= 0.67,P< 0.001) and ADC (r= 0.58,P< 0.001) andwas lower (P< 0.05) in malignant lesions than benign and normal tissues. Cellular content correlated inversely with the fastsignal fraction (r=–0.67,P< 0.001) and ADC (r=–0.61,P< 0.001) and was different (P< 0.05) between malignant,benign, and normal tissues.Data Conclusion:Ourfindings suggest stromal collagen content increases diffusivity observed by MRI and is associatedwith higher ADC and fast signal fraction of the biexponential modelnb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleStromal collagen content in breast tumors correlates with in vivo diffusion-weighted imaging: A comparison of multi b-value DWI with histologic specimen from benign and malignant breast lesionsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1-11nb_NO
dc.source.journalJournal of Magnetic Resonance Imagingnb_NO
dc.identifier.doi10.1002/jmri.27018
dc.identifier.cristin1771528
dc.description.localcode© 2019 The Authors. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproductionin any medium, provided the original work is properly cited and is not used for commercial purposesnb_NO
cristin.unitcode1920,4,0,0
cristin.unitcode194,66,20,0
cristin.unitcode194,65,25,0
cristin.unitcode194,65,15,0
cristin.unitnameKlinikk for bildediagnostikk
cristin.unitnameInstitutt for fysikk
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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