Pupillometric and Perceptual Approaches Provide Independent Estimates of Melanopsin Activity in Humans

dc.contributor.author Woelders, T.
dc.contributor.author Didikoglu, A.
dc.contributor.author Bickerstaff, L.
dc.contributor.author Brown, T.M.
dc.contributor.author Lucas, R.J.
dc.date.accessioned 2025-02-05T09:48:47Z
dc.date.available 2025-02-05T09:48:47Z
dc.date.issued 2025
dc.description.abstract Study Objectives: Melanopsin-expressing retinal ganglion cells, which provide light information to time sleep and entrain circadian clocks, also influence perceived brightness raising the possibility that psychophysical paradigms could be used to explore the origins and implications of variability in melanopic sensitivity. We aimed to develop accessible psychophysical tests of melanopic vision and relate outcomes with a pupillometric measure of melanopsin function (post-illumination pupil response) and prior light exposure. Methods: Individually calibrated pairs of isoluminant stimuli differing in melanopic radiance from a four primary source were presented sequentially with superimposed random color offsets in a two alternative forced choice brightness preference paradigm to 41 naïve adult participants with personal light exposure data for the prior 7 days and post-illumination pupil response measures defined by comparing maintained pupil constriction for luminance matched “red” vs “blue” pulses. Results: Across participants we observed the expected tendency to report positive melanopsin contrast stimuli as “brighter” (one-tailed t-test p < 0.001), but with substantial inter-individual variability in both sensitivity (melanopsin contrast at criterion preference p = 0.75) and amplitude (preference at maximum melanopic contrast). There was little correlation between these psychophysical outcomes and post-illumination pupil response magnitude, or between either psychophysical or post-illumination pupil response measures and light history metrics (pairwise Pearson correlation coefficients -0.5> < 0.5). Random forest machine learning failed to satisfactorily predict outcome for either psychophysical or post-illumination pupil response measures based upon these inputs. Conclusions: Our findings reveal that estimates of melanopic function provided by perceptual and pupillometric paradigms can be largely independent of one another and of recent history of light exposure. © The Author(s) 2024. Published by Oxford University Press on behalf of Sleep Research Society. en_US
dc.description.sponsorship Wellcome Trust, WT, (210684/Z/18/Z); Wellcome Trust, WT en_US
dc.identifier.doi 10.1093/sleep/zsae289
dc.identifier.issn 0161-8105
dc.identifier.issn 1550-9109
dc.identifier.scopus 2-s2.0-85218474716
dc.identifier.uri https://doi.org/10.1093/sleep/zsae289
dc.identifier.uri https://hdl.handle.net/11147/15304
dc.language.iso en en_US
dc.publisher Oxford University Press en_US
dc.relation.ispartof Sleep en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Brightness en_US
dc.subject Contrast en_US
dc.subject Light Sensitivity en_US
dc.subject Melanopsin en_US
dc.subject Post-Illumination Pupil Response en_US
dc.subject Silent Substitution en_US
dc.title Pupillometric and Perceptual Approaches Provide Independent Estimates of Melanopsin Activity in Humans en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Didikoglu, Altug/0000-0002-5582-6956
gdc.author.id Bickerstaff, Lucien/0000-0002-2683-8130
gdc.author.id Didikoglu, Altug / 0000-0002-5582-6956 en_US
gdc.author.id Bickerstaff, Lucien / 0000-0002-2683-8130 en_US
gdc.author.scopusid 57194521574
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gdc.bip.impulseclass C5
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gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology en_US
gdc.description.departmenttemp Woelders T., Division of Neuroscience, School of Biological Sciences, Faculty of Biology Medicine and Health, Centre for Biological Timing, University of Manchester, Manchester, United Kingdom; Didikoglu A., Division of Neuroscience, School of Biological Sciences, Faculty of Biology Medicine and Health, Centre for Biological Timing, University of Manchester, Manchester, United Kingdom, Department of Neuroscience, Izmir Institute of Technology, Gulbahce, Urla, Izmir, Turkey; Bickerstaff L., Max Planck Institute for Biological Cybernetics, Translational Sensory & Circadian Neuroscience, Tübingen, Germany, Department Health and Sport Sciences, TUM School of Medicine and Health, Technical University of Munich, Munich, Germany; Brown T.M., Division of Diabetes Endocrinology and Gastroenterology, School of Medical Sciences, Faculty of Biology Medicine and Health, Centre for Biological Timing, University of Manchester, Manchester, United Kingdom; Lucas R.J., Division of Neuroscience, School of Biological Sciences, Faculty of Biology Medicine and Health, Centre for Biological Timing, University of Manchester, Manchester, United Kingdom en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 48 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.openalex W4405400452
gdc.identifier.pmid 39672888
gdc.identifier.wos WOS:001387890400001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype HYBRID
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gdc.oaire.impulse 0.0
gdc.oaire.influence 2.635068E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Male
gdc.oaire.keywords Adult
gdc.oaire.keywords Retinal Ganglion Cells
gdc.oaire.keywords Light
gdc.oaire.keywords Rod Opsins
gdc.oaire.keywords Basic Science of Sleep and Circadian Rhythms
gdc.oaire.keywords Pupil
gdc.oaire.keywords Reflex, Pupillary
gdc.oaire.keywords Young Adult
gdc.oaire.keywords Psychophysics
gdc.oaire.keywords Humans
gdc.oaire.keywords Female
gdc.oaire.keywords Photic Stimulation
gdc.oaire.popularity 3.0009937E-9
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gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
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relation.isOrgUnitOfPublication.latestForDiscovery b03386e1-8d31-452b-abf2-690619843aa0

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