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Insights for mfVEPs from perimetry using large spatial frequency-doubling and near frequency-doubling stimuli in glaucoma.

dc.contributor.authorAbdullah, Siti Nurliyana
dc.contributor.authorSanderson, Gordon F
dc.contributor.authorHusni, Mohd Aziz
dc.contributor.authorMaddess, Ted
dc.date.accessioned2023-01-18T02:51:50Z
dc.date.issued2020
dc.date.updated2021-11-28T07:36:21Z
dc.description.abstractPurpose To compare two forms of perimetry that use large contrast-modulated grating stimuli in terms of: their relative diagnostic power, their independent diagnostic information about glaucoma and their utility for mfVEPs. We evaluated a contrast-threshold mfVEP in normal controls using the same stimuli as one of the tests. Methods We measured psychophysical contrast thresholds in one eye of 16 control subjects and 19 patients aged 67.8 ± 5.65 and 71.9 ± 7.15, respectively, (mean ± SD). Patients ranged in disease severity from suspects to severe glaucoma. We used the 17-region FDT-perimeter C20-threshold program and a custom 9-region test (R9) with similar visual field coverage. The R9 stimuli scaled their spatial frequencies with eccentricity and were modulated at lower temporal frequencies than C20 and thus did not display a clear spatial frequency-doubling (FD) appearance. Based on the overlapping areas of the stimuli, we transformed the C20 results to 9 measures for direct comparison with R9. We also compared mfVEP-based and psychophysical contrast thresholds in 26 younger (26.6 ± 7.3 y, mean ± SD) and 20 older normal control subjects (66.5 ± 7.3 y) control subjects using the R9 stimuli. Results The best intraclass correlations between R9/C20 thresholds were for the central and outer regions: 0.82 ± 0.05 (mean ± SD, p ≤ 0.0001). The areas under receiver operator characteristic plots for C20 and R9 were as high as 0.99 ± 0.012 (mean ± SE). Canonical correlation analysis (CCA) showed significant correlation (r = 0.638, p = 0.029) with 1 dimension of the C20 and R9 data, suggesting that the lower and higher temporal frequency tests probed the same neural mechanism(s). Low signal quality made the contrast-threshold mfVEPs non-viable. The resulting mfVEP thresholds were limited by noise to artificially high contrasts, which unlike the psychophysical versions, were not correlated with age. Conclusion The lower temporal frequency R9 stimuli had similar diagnostic power to the FDT-C20 stimuli. CCA indicated the both stimuli drove similar neural mechanisms, possibly suggesting no advantage of FD stimuli for mfVEPs. Given that the contrast-threshold mfVEPs were non-viable, we used the present and published results to make recommendations for future mfVEP tests. Introductionen_AU
dc.description.sponsorshipintramural funding from the Australian National University.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0012-4486en_AU
dc.identifier.urihttp://hdl.handle.net/1885/282852
dc.language.isoen_AUen_AU
dc.provenancehttps://v2.sherpa.ac.uk/id/publication/17340/..."accepted version can be archived in institutional repository" from Sherpa/Romeo site as at 04/02/2021
dc.publisherSpringeren_AU
dc.relationhttp://purl.org/au-research/grants/arc/CE0561903en_AU
dc.rights© 2020 The authorsen_AU
dc.sourceDocumenta Ophthalmologicaen_AU
dc.subjectGlaucomaen_AU
dc.subjectFrequency doublingen_AU
dc.subjectPerimetryen_AU
dc.subjectNeural mechanismsen_AU
dc.subjectMultifocal VEPsen_AU
dc.titleInsights for mfVEPs from perimetry using large spatial frequency-doubling and near frequency-doubling stimuli in glaucoma.en_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Access
local.bibliographicCitation.lastpage55en_AU
local.bibliographicCitation.startpage44en_AU
local.contributor.affiliationAbdullah, Siti Nurliyana, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSanderson, Gordon F, Otago Universityen_AU
local.contributor.affiliationHusni, Mohd Aziz, Selayang Hospitalen_AU
local.contributor.affiliationMaddess, Ted, College of Health and Medicine, ANUen_AU
local.contributor.authoruidAbdullah, Siti Nurliyana, u4703359en_AU
local.contributor.authoruidMaddess, Ted, u8103614en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor320602 - Medical biotechnology diagnostics (incl. biosensors)en_AU
local.identifier.absseo280112 - Expanding knowledge in the health sciencesen_AU
local.identifier.ariespublicationu6269649xPUB833en_AU
local.identifier.citationvolume141en_AU
local.identifier.doi10.1007/s10633-020-09750-7en_AU
local.identifier.scopusID2-s2.0-85079214351
local.publisher.urlhttps://link.springer.com/en_AU
local.type.statusAccepted Versionen_AU

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