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dc.date.accessioned2022-03-14T18:18:43Z
dc.date.available2022-03-14T18:18:43Z
dc.date.created2022-02-10T09:56:46Z
dc.date.issued2021
dc.identifier.citationBascuñana, Pablo Brackhan, Mirjam Pahnke, Jens . Machine Learning-Supported Analyses Improve Quantitative Histological Assessments of Amyloid-β Deposits and Activated Microglia. Journal of Alzheimer's Disease. 2021, 79(2), 597-605
dc.identifier.urihttp://hdl.handle.net/10852/92471
dc.description.abstractBackground: Detailed pathology analysis and morphological quantification is tedious and prone to errors. Automatic image analysis can help to increase objectivity and reduce time. Here, we present the evaluation of the DeePathology STUDIO™ for automatic analysis of histological whole-slide images using machine learning/artificial intelligence. Objective: To evaluate and validate the use of DeePathology STUDIO for the analysis of histological slides at high resolution. Methods: We compared the DeePathology STUDIO and our current standard method using macros in AxioVision for the analysis of amyloid-β (Aβ) plaques and microglia in APP-transgenic mice at different ages. We analyzed density variables and total time invested with each approach. In addition, we correlated Aβ concentration in brain tissue measured by ELISA with the results of Aβ staining analysis. Results: DeePathology STUDIO showed a significant decrease of the time for establishing new analyses and the total analysis time by up to 90%. On the other hand, both approaches showed similar quantitative results in plaque and activated microglia density in the different experimental groups. DeePathology STUDIO showed higher sensitivity and accuracy for small-sized plaques. In addition, DeePathology STUDIO allowed the classification of plaques in diffuse- and dense-packed, which was not possible with our traditional analysis. Conclusion: DeePathology STUDIO substantially reduced the effort needed for a new analysis showing comparable quantitative results to the traditional approach. In addition, it allowed including different objects (categories) or cell types in a single analysis, which is not possible with conventional methods.
dc.languageEN
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.titleMachine Learning-Supported Analyses Improve Quantitative Histological Assessments of Amyloid-β Deposits and Activated Microglia
dc.typeJournal article
dc.creator.authorBascuñana, Pablo
dc.creator.authorBrackhan, Mirjam
dc.creator.authorPahnke, Jens
cristin.unitcode185,53,18,13
cristin.unitnameAvdeling for patologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1999820
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Alzheimer's Disease&rft.volume=79&rft.spage=597&rft.date=2021
dc.identifier.jtitleJournal of Alzheimer's Disease
dc.identifier.volume79
dc.identifier.issue2
dc.identifier.startpage597
dc.identifier.endpage605
dc.identifier.doihttps://doi.org/10.3233/JAD-201120
dc.identifier.urnURN:NBN:no-95053
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1387-2877
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/92471/1/Machine%2BLearning-Supported%2BAnalyses.pdf
dc.type.versionPublishedVersion
dc.relation.projectNFR/251290
dc.relation.projectHSØ/2016062
dc.relation.projectEC/H2020/643417
dc.relation.projectNFR/295910
dc.relation.projectNFR/260786
dc.relation.projectHSØ/2019054
dc.relation.projectCHILDCANCER/19008
dc.relation.projectHSØ/2019055


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Attribution-NonCommercial 4.0 International
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