SegAE: Unsupervised white matter lesion segmentation from brain MRIs using a CNN autoencoder

dc.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorAtlason, Hans
dc.contributor.authorLove, Askell
dc.contributor.authorSigurdsson, Sigurdur
dc.contributor.authorGudnason, Vilmundur
dc.contributor.authorEllingsen, Lotta María
dc.contributor.departmentRafmagns- og tölvuverkfræðideild (HÍ)en_US
dc.contributor.departmentFaculty of Electrical and Computer Engineering (UI)en_US
dc.contributor.departmentLæknadeild (HÍ)en_US
dc.contributor.departmentFaculty of Medicine (UI)en_US
dc.contributor.schoolVerkfræði- og náttúruvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Engineering and Natural Sciences (UI)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.date.accessioned2020-06-18T11:30:15Z
dc.date.available2020-06-18T11:30:15Z
dc.date.issued2019
dc.descriptionPublisher's version (útgefin grein)en_US
dc.description.abstractWhite matter hyperintensities (WMHs) of presumed vascular origin are frequently observed in magnetic resonance images (MRIs) of the elderly. Detection and quantification of WMHs is important to help doctors make diagnoses and evaluate prognosis of their elderly patients, and once quantified, these can act as biomarkers in clinical research studies. Manual delineation of WMHs can be both time-consuming and inconsistent, hence, automatic segmentation methods are often preferred. However, fully automatic methods can be challenging to construct due to the variability in lesion load, placement of lesions, and voxel intensities. Several state-of-the-art lesion segmentation methods based on supervised Convolutional Neural Networks (CNNs) have been proposed. These approaches require manually delineated lesions for training the parameters of the network. Here we present a novel approach for WMH segmentation using a CNN trained in an unsupervised manner, by reconstructing multiple MRI sequences as weighted sums of segmentations of WMHs and tissues present in the images. After training, our method can be used to segment new images that are not part of the training set to provide fast and robust segmentation of WMHs in a matter of seconds per subject. Comparisons with state-of-the-art WMH segmentation methods evaluated on ground truth manual labels from two distinct data sets and six different scanners indicate that the proposed method works well at generating accurate WMH segmentations without the need for manual delineations.en_US
dc.description.sponsorshipThis work was supported by RANNIS (The Icelandic Centre for Research ) through grant 173942-051 . We thank Burkni Palsson for a valuable discussion about hyperspectral unmixing using a neural network autoencoder, and Nicholas J. Tustison for valuable insights on N4 bias correction on FLAIR images with WMHs.en_US
dc.description.versionPeer Revieweden_US
dc.format.extent102085en_US
dc.identifier.citationAtlason, H. E., et al. (2019). "SegAE: Unsupervised white matter lesion segmentation from brain MRIs using a CNN autoencoder." NeuroImage: Clinical 24: 102085.en_US
dc.identifier.doi10.1016/j.nicl.2019.102085
dc.identifier.issn2213-1582
dc.identifier.journalNeuroImage: Clinicalen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/1894
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofseriesNeuroImage: Clinical;24
dc.relation.urlhttps://www.sciencedirect.com/science/article/pii/S2213158219304322?via%3Dihuben_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAutoencoderen_US
dc.subjectBrainen_US
dc.subjectCNNen_US
dc.subjectDeep learningen_US
dc.subjectSegmentationen_US
dc.subjectWhite matter hyperintensityen_US
dc.subjectHeilinnen_US
dc.subjectMyndgreining (læknisfræði)en_US
dc.titleSegAE: Unsupervised white matter lesion segmentation from brain MRIs using a CNN autoencoderen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.licenseThis is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/).en_US

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