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Comparing Objective Perimetry, Matrix Perimetry, and Regional Retinal Thickness in Mild Diabetic Macular Edema

dc.contributor.authorRai, Bhim Bahadur
dc.contributor.authorMaddess, Ted
dc.contributor.authorCarle, Corinne Frances
dc.contributor.authorRohan, Emilie
dc.contributor.authorvan Kleef, Joshua
dc.contributor.authorBarry, Richard
dc.contributor.authorEssex, Rohan
dc.contributor.authorNolan, Christopher
dc.contributor.authorSABETI, Faran
dc.date.accessioned2023-06-20T04:46:33Z
dc.date.available2023-06-20T04:46:33Z
dc.date.issued2021
dc.date.updated2022-04-03T08:20:27Z
dc.description.abstractPurpose: To compare per-region macular sensitivity and delay from objective perimetry with Matrix perimetry and retinal thickness in mild diabetic macular edema (DMO). Methods: Thirty-three patients with type 2 diabetes (T2D) aged 59.2 ± 10.5 years participated in a longitudinal study. Macular thickness, sensitivities and delays from the objectiveFIELD Analyzer (OFA), and Matrix perimeter sensitivities were mapped onto a common spatial layout to compute per-region correlations between structure/function measures. A generalized linear mixed-effects logistic regression model determined which variables contributed to clinical diagnosis of DMO. Results: For OFA, the mean sensitivity differences compared with normal in patients with T2D were negative and the mean delay differences positive, indicating lowered sensitivities and prolonged delays, both increasing with diabetes duration. Shorter diabetes duration could produce either localized peripheral hypersensitivities or shorter delays. Functional change could occur when retinal thickness was stable. Peripheral macular thickness correlated with central and peripheral OFA sensitivity and delay, all P < 0.0012 in DMO and a median of P = 0.001 without DMO; this was not true for Matrix sensitivities. The logistic model determined that peripheral thickness, OFA sensitivity (P = 0.043), and time in the study (P = 0.001) contribute independently to the odds of DMO versus no DMO. Conclusions: Mean sensitivities decreased and mean delays increased with duration of diabetes. Peripheral macular thickness correlated significantly with central and peripheral macular OFA sensitivity and delay. Peripheral macular thickness and functional measures may provide sensitive prognostic data. Translational Relevance: Functional loss can precede structural change in DMO, so including such functional assessment for deciding on treatment may be beneficial.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn2164-2591en_AU
dc.identifier.urihttp://hdl.handle.net/1885/293609
dc.language.isoen_AUen_AU
dc.provenanceThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licenseen_AU
dc.publisherARVOen_AU
dc.rights© 2021 The Author(s)en_AU
dc.rights.licenseCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_AU
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_AU
dc.sourceTranslational Vision Science & Technologyen_AU
dc.subjectdiabetic macular edemaen_AU
dc.subjectobjective perimetryen_AU
dc.subjectmultifocal pupillographyen_AU
dc.subjectretinal functionen_AU
dc.subjectstructure and function correlationen_AU
dc.titleComparing Objective Perimetry, Matrix Perimetry, and Regional Retinal Thickness in Mild Diabetic Macular Edemaen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue13en_AU
local.bibliographicCitation.lastpage12en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationRai, Bhim, College of Health and Medicine, ANUen_AU
local.contributor.affiliationMaddess, Ted, College of Health and Medicine, ANUen_AU
local.contributor.affiliationCarle, Corinne, College of Health and Medicine, ANUen_AU
local.contributor.affiliationRohan, Emilie, College of Health and Medicine, ANUen_AU
local.contributor.affiliationVan Kleef, Joshua, College of Health and Medicine, ANUen_AU
local.contributor.affiliationBarry, Richard, The Canberra Hospitalen_AU
local.contributor.affiliationEssex, Rohan, College of Health and Medicine, ANUen_AU
local.contributor.affiliationNolan, Christopher, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSabeti, Faran, College of Health and Medicine, ANUen_AU
local.contributor.authoruidRai, Bhim, u5897741en_AU
local.contributor.authoruidMaddess, Ted, u8103614en_AU
local.contributor.authoruidCarle, Corinne, u4117988en_AU
local.contributor.authoruidRohan, Emilie, u5687443en_AU
local.contributor.authoruidVan Kleef, Joshua, u3551948en_AU
local.contributor.authoruidEssex, Rohan, u5102645en_AU
local.contributor.authoruidNolan, Christopher, u1820721en_AU
local.contributor.authoruidSabeti, Faran, u4489908en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor320602 - Medical biotechnology diagnostics (incl. biosensors)en_AU
local.identifier.absseo200101 - Diagnosis of human diseases and conditionsen_AU
local.identifier.ariespublicationa383154xPUB23553en_AU
local.identifier.citationvolume10en_AU
local.identifier.doi10.1167/tvst.10.13.32en_AU
local.identifier.scopusID2-s2.0-85122276521
local.publisher.urlhttps://tvst.arvojournals.org/en_AU
local.type.statusPublished Versionen_AU

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