Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33068
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dc.contributor.authorLemmens, Sophie-
dc.contributor.authorVan Craenendonck, Toon-
dc.contributor.authorVan Eijgen, Jan-
dc.contributor.authorDe Groef, Lies-
dc.contributor.authorBRUFFAERTS, Rose-
dc.contributor.authorde Jesus, Danilo Andrade-
dc.contributor.authorCharle, Wouter-
dc.contributor.authorJayapala, Murali-
dc.contributor.authorSunaric-Megevand, Gordana-
dc.contributor.authorStandaert, Arnout-
dc.contributor.authorTHEUNIS, Jan-
dc.contributor.authorVan Keer, Karel-
dc.contributor.authorVandenbulcke, Mathieu-
dc.contributor.authorMoons, Lieve-
dc.contributor.authorVandenberghe, Rik-
dc.contributor.authorStalmans, Ingeborg-
dc.contributor.authorDE BOEVER, Patrick-
dc.date.accessioned2021-01-07T14:44:11Z-
dc.date.available2021-01-07T14:44:11Z-
dc.date.issued2020-
dc.date.submitted2021-01-06T15:41:09Z-
dc.identifier.citationAlzheimers Research & Therapy, 12 (1) (Art N° 144)-
dc.identifier.urihttp://hdl.handle.net/1942/33068-
dc.description.abstractIntroduction The eye offers potential for the diagnosis of Alzheimer's disease (AD) with retinal imaging techniques being explored to quantify amyloid accumulation and aspects of neurodegeneration. To assess these changes, this proof-of-concept study combined hyperspectral imaging and optical coherence tomography to build a classification model to differentiate between AD patients and controls. Methods In a memory clinic setting, patients with a diagnosis of clinically probable AD (n = 10) or biomarker-proven AD (n = 7) and controls (n = 22) underwent non-invasive retinal imaging with an easy-to-use hyperspectral snapshot camera that collects information from 16 spectral bands (460-620 nm, 10-nm bandwidth) in one capture. The individuals were also imaged using optical coherence tomography for assessing retinal nerve fiber layer thickness (RNFL). Dedicated image preprocessing analysis was followed by machine learning to discriminate between both groups. Results Hyperspectral data and retinal nerve fiber layer thickness data were used in a linear discriminant classification model to discriminate between AD patients and controls. Nested leave-one-out cross-validation resulted in a fair accuracy, providing an area under the receiver operating characteristic curve of 0.74 (95% confidence interval [0.60-0.89]). Inner loop results showed that the inclusion of the RNFL features resulted in an improvement of the area under the receiver operating characteristic curve: for the most informative region assessed, the average area under the receiver operating characteristic curve was 0.70 (95% confidence interval [0.55, 0.86]) and 0.79 (95% confidence interval [0.65, 0.93]), respectively. The robust statistics used in this study reduces the risk of overfitting and partly compensates for the limited sample size. Conclusions This study in a memory-clinic-based cohort supports the potential of hyperspectral imaging and suggests an added value of combining retinal imaging modalities. Standardization and longitudinal data on fully amyloid-phenotyped cohorts are required to elucidate the relationship between retinal structure and cognitive function and to evaluate the robustness of the classification model.-
dc.description.sponsorshipSophie Lemmens and Jan Van Eijgen are holders of a joint VITO-UZ Leuven PhD grant. Part of this research work has been funded in the context of the VITO-UZ Leuven HERALD project that was granted by the ATTRACT consortium, which received funding from the European Union's Horizon 2020 Research and Innovation Programme (2014-2020). Lies De Groef and Rose Bruffaerts are postdoctoral fellows of the Research Foundation Flanders.-
dc.language.isoen-
dc.publisherBMC-
dc.rights© The Author(s). 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.-
dc.subject.otherRetina-
dc.subject.otherBrain-
dc.subject.otherNeurodegeneration-
dc.subject.otherCognitive impairment-
dc.subject.otherAlzheimer&#8217-
dc.subject.others disease-
dc.subject.otherAmyloid-beta (A&#946-
dc.subject.other)-
dc.subject.otherHyperspectral imaging-
dc.subject.otherMachine learning-
dc.subject.otherBiomarker-
dc.titleCombination of snapshot hyperspectral retinal imaging and optical coherence tomography to identify Alzheimer’s disease patients-
dc.typeJournal Contribution-
dc.identifier.issue1-
dc.identifier.volume12-
local.format.pages13-
local.bibliographicCitation.jcatA1-
dc.description.notesLemmens, S (corresponding author), Univ Hosp UZ Leuven, Dept Ophthalmol, Herestr 49, B-3000 Leuven, Belgium.; Lemmens, S (corresponding author), Katholieke Univ Leuven, Res Grp Ophthalmol, Biomed Sci Grp, Dept Neurosci, Herestr 49, B-3000 Leuven, Belgium.; Lemmens, S (corresponding author), VITO Flemish Inst Technol Res, Hlth Unit, Boeretang 200, B-2400 Mol, Belgium.-
dc.description.notessophie.1.lemmens@uzleuven.be-
dc.description.otherLemmens, S (corresponding author), Univ Hosp UZ Leuven, Dept Ophthalmol, Herestr 49, B-3000 Leuven, Belgium ; Katholieke Univ Leuven, Res Grp Ophthalmol, Biomed Sci Grp, Dept Neurosci, Herestr 49, B-3000 Leuven, Belgium. VITO Flemish Inst Technol Res, Hlth Unit, Boeretang 200, B-2400 Mol, Belgium. sophie.1.lemmens@uzleuven.be-
local.publisher.placeCAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr144-
dc.identifier.doi10.1186/s13195-020-00715-1-
dc.identifier.isiWOS:000594161200001-
dc.contributor.orcidTheunis, Jan/0000-0002-4191-5667; De Boever, Patrick/0000-0002-5197-8215-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.description.affiliation[Lemmens, Sophie; Van Eijgen, Jan; Van Keer, Karel; Stalmans, Ingeborg] Univ Hosp UZ Leuven, Dept Ophthalmol, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[Lemmens, Sophie; Van Eijgen, Jan; de Jesus, Danilo Andrade; Van Keer, Karel; Stalmans, Ingeborg] Katholieke Univ Leuven, Res Grp Ophthalmol, Biomed Sci Grp, Dept Neurosci, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[Lemmens, Sophie; Van Craenendonck, Toon; Van Eijgen, Jan; Standaert, Arnout; Theunis, Jan; De Boever, Patrick] VITO Flemish Inst Technol Res, Hlth Unit, Boeretang 200, B-2400 Mol, Belgium.-
local.description.affiliation[De Groef, Lies; Moons, Lieve] Katholieke Univ Leuven, Neural Circuit Dev & Regenerat Res Grp, Dept Biol, Naamsestr 61, B-3000 Leuven, Belgium.-
local.description.affiliation[Bruffaerts, Rose; Vandenberghe, Rik] Katholieke Univ Leuven, Dept Neurosci, Lab Cognit Neurol, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[Bruffaerts, Rose; Vandenberghe, Rik] Univ Hosp UZ Leuven, Dept Neurol, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[Charle, Wouter; Jayapala, Murali] IMEC, Kapeldreef 75, B-3001 Leuven, Belgium.-
local.description.affiliation[Sunaric-Megevand, Gordana] Mem A Rothschild, Clin Res Ctr, 22 Chemin Beau Soleil, CH-1208 Geneva, Switzerland.-
local.description.affiliation[Vandenbulcke, Mathieu] Univ Hosp Leuven, Div Psychiat, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[Vandenberghe, Rik] Alzheimer Res Ctr KU Leuven, Leuven Brain Inst, Herestr 49, B-3000 Leuven, Belgium.-
local.description.affiliation[De Boever, Patrick] Hasselt Univ, Ctr Environm Sci, B-3590 Diepenbeek, Belgium.-
local.description.affiliation[De Boever, Patrick] Univ Antwerp, Dept Biol, Univ Pl 1, B-2610 Antwerp, Belgium.-
local.uhasselt.internationalyes-
item.contributorLemmens, Sophie-
item.contributorVan Craenendonck, Toon-
item.contributorVan Eijgen, Jan-
item.contributorDe Groef, Lies-
item.contributorBRUFFAERTS, Rose-
item.contributorde Jesus, Danilo Andrade-
item.contributorCharle, Wouter-
item.contributorJayapala, Murali-
item.contributorSunaric-Megevand, Gordana-
item.contributorStandaert, Arnout-
item.contributorTHEUNIS, Jan-
item.contributorVan Keer, Karel-
item.contributorVandenbulcke, Mathieu-
item.contributorMoons, Lieve-
item.contributorVandenberghe, Rik-
item.contributorStalmans, Ingeborg-
item.contributorDE BOEVER, Patrick-
item.fullcitationLemmens, Sophie; Van Craenendonck, Toon; Van Eijgen, Jan; De Groef, Lies; BRUFFAERTS, Rose; de Jesus, Danilo Andrade; Charle, Wouter; Jayapala, Murali; Sunaric-Megevand, Gordana; Standaert, Arnout; THEUNIS, Jan; Van Keer, Karel; Vandenbulcke, Mathieu; Moons, Lieve; Vandenberghe, Rik; Stalmans, Ingeborg & DE BOEVER, Patrick (2020) Combination of snapshot hyperspectral retinal imaging and optical coherence tomography to identify Alzheimer’s disease patients. In: Alzheimers Research & Therapy, 12 (1) (Art N° 144).-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
item.validationecoom 2021-
crisitem.journal.eissn1758-9193-
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