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Semiquantitative measurement of murine bleomycin-induced lung fibrosis in in vivo and postmortem conditions using microcomputed tomography: Correlation with pathologic scores - Initial results

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dc.contributor.authorLee, H.J.-
dc.contributor.authorGoo, J.M.-
dc.contributor.authorKim, N.R.-
dc.contributor.authorKim, M.A.-
dc.contributor.authorChung, D.H.-
dc.contributor.authorSon, K.-R.-
dc.contributor.authorKim, H.-C.-
dc.contributor.authorLee, C.H.-
dc.contributor.authorPark, C.M.-
dc.contributor.authorChun, E.J.-
dc.contributor.authorIm, J.-G.-
dc.date.accessioned2024-08-08T01:49:20Z-
dc.date.available2024-08-08T01:49:20Z-
dc.date.created2024-07-25-
dc.date.created2024-07-25-
dc.date.issued2008-
dc.identifier.citationInvestigative Radiology, Vol.43 No.6, pp.453-460-
dc.identifier.issn0020-9996-
dc.identifier.urihttps://hdl.handle.net/10371/208416-
dc.description.abstractOBJECTIVE: To evaluate whether the semiquantification of lung inflammation and fibrosis in murine bleomycin-induced lung fibrosis using micro-computed tomography (micro-CT) in in vivo and postmortem conditions is feasible, and to correlate micro-CT and pathologic scores. MATERIALS AND METHODS: Bleomycin-induced lung fibrosis was created by intratracheally instilling 3 mg/kg of bleomycin into C57BL/6 mice. Mice were allocated randomly to 2-week, 4-week, and 8-week follow-up groups. In each group, in vivo and follow-up postmortem micro-CT were performed using a voxel size of 35 × 35 × 35 μm. Ground-glass opacity (GGO), consolidation, parenchymal lines, honeycombing, and peripheral bronchial dilatation were scored on micro-CT images in a semiquantitative fashion, whereas inflammation and fibrosis were scored histopathologically. The confidence levels of micro-CT findings were also scored. Correlations between micro-CT and pathologic findings were examined using Spearman rank correlation analysis, and differences between CT scores and confidence levels for in vivo and postmortem micro-CT were subjected to Wilcoxon signed rank testing. Agreements between in vivo and postmortem micro-CT scores were tested using weighted κ statistics. RESULTS: Consolidation in vivo (r = 0.46) and at postmortem (r = 0.39) and GGO in vivo (r = 0.31) by micro-CT showed fair to moderate correlation with pathologic inflammation scores (P < 0.001). By in vivo and postmortem micro-CT, parenchymal lines (r = 0.72 vs. 0.83) showed good to excellent and peripheral bronchial dilatation (r = 0.47 vs. 0.68) showed moderate to good correlation with pathologic fibrosis scores (P < 0.001). For GGO, consolidation, peripheral bronchial dilatation, and parenchymal lines, fair to moderate agreement was obtained between in vivo and postmortem micro-CT. However, confidence levels for peripheral bronchial dilatation, parenchymal lines, and honeycombing were significantly higher by postmortem micro-CT (P < 0.001). CONCLUSIONS: Micro-CT scores and pathologic scores were found to be well correlated by in vivo and postmortem micro-CT. Although agreements between in vivo and postmortem micro-CT were significant, the confidence levels for fibrosis-related CT findings were significantly higher by postmortem micro-CT. © 2008 Lippincott Williams & Wilkins, Inc.-
dc.language영어-
dc.publisherLippincott Williams & Wilkins Ltd.-
dc.titleSemiquantitative measurement of murine bleomycin-induced lung fibrosis in in vivo and postmortem conditions using microcomputed tomography: Correlation with pathologic scores - Initial results-
dc.typeArticle-
dc.identifier.doi10.1097/RLI.0b013e31816900ec-
dc.citation.journaltitleInvestigative Radiology-
dc.identifier.wosid000256204200016-
dc.identifier.scopusid2-s2.0-44449174438-
dc.citation.endpage460-
dc.citation.number6-
dc.citation.startpage453-
dc.citation.volume43-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorGoo, J.M.-
dc.contributor.affiliatedAuthorPark, C.M.-
dc.contributor.affiliatedAuthorIm, J.-G.-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordAuthorBleomycin-
dc.subject.keywordAuthorFibrosis-
dc.subject.keywordAuthorLung-
dc.subject.keywordAuthorMicrocomputed tomography-
dc.subject.keywordAuthorMurine-
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  • Department of Medicine
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