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dc.contributor.authorLøchen, Aili Røtterud
dc.contributor.authorKolskår, Knut-Kristian
dc.contributor.authorde Lange, Ann-Marie Glasø
dc.contributor.authorSneve, Markus Handal
dc.contributor.authorHaatveit, Beathe
dc.contributor.authorLagerberg, Trine Vik
dc.contributor.authorUeland, Torill
dc.contributor.authorMelle, Ingrid
dc.contributor.authorAndreassen, Ole
dc.contributor.authorWestlye, Lars Tjelta
dc.contributor.authorAlnæs, Dag
dc.date.accessioned2023-09-19T05:37:07Z
dc.date.available2023-09-19T05:37:07Z
dc.date.created2023-02-25T14:35:08Z
dc.date.issued2023
dc.identifier.citationHeliyon. 2023, 9 (2) .en_US
dc.identifier.issn2405-8440
dc.identifier.urihttps://hdl.handle.net/11250/3090213
dc.description.abstractAbstract Objective Low-level sensory disruption is hypothesized as a precursor to clinical and cognitive symptoms in severe mental disorders. We compared visual discrimination performance in patients with schizophrenia spectrum disorder or bipolar disorder with healthy controls, and investigated associations with clinical symptoms and IQ. Methods Patients with schizophrenia spectrum disorder (n = 32), bipolar disorder (n = 55) and healthy controls (n = 152) completed a computerized visual discrimination task. Participants responded whether the latter of two consecutive grids had higher or lower spatial frequency, and discrimination thresholds were estimated using an adaptive maximum likelihood procedure. Case-control differences in threshold were assessed using linear regression, F-test and post-hoc pair-wise comparisons. Linear models were used to test for associations between visual discrimination threshold and psychotic symptoms derived from the PANSS and IQ assessed using the Matrix Reasoning and Vocabulary subtests from the Wechsler Abbreviated Scale of Intelligence (WASI). Results Robust regression revealed a significant main effect of diagnosis on discrimination threshold (robust F = 6.76, p = .001). Post-hoc comparisons revealed that patients with a schizophrenia spectrum disorder (mean = 14%, SD = 0.08) had higher thresholds compared to healthy controls (mean = 10.8%, SD = 0.07, β = 0.35, t = 3.4, p = .002), as did patients with bipolar disorder (12.23%, SD = 0.07, β = 0.21, t = 2.42, p = .04). There was no significant difference between bipolar disorder and schizophrenia (β = −0.14, t = −1.2, p = .45). Linear models revealed negative associations between IQ and threshold across all participants when controlling for diagnostic group (β = −0.3, t = −3.43, p = .0007). This association was found within healthy controls (t = −3.72, p = .0003) and patients with bipolar disorder (t = −2.53, p = .015), and no significant group by IQ interaction on threshold (F = 0.044, p = .97). There were no significant associations between PANSS domain scores and discrimination threshold. Conclusion Patients with schizophrenia spectrum or bipolar disorders exhibited higher visual discrimination thresholds than healthy controls, supporting early visual deficits among patients with severe mental illness. Discrimination threshold was negatively associated with IQ among healthy controls and bipolar disorder patients. These findings elucidate perception-related disease mechanisms in severe mental illness, which warrants replication in independent samples.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectvisual discriminationen_US
dc.subjectspatial frequencyen_US
dc.subjectbipolar disorderen_US
dc.subjectschizophreniaen_US
dc.subjectmental illnessen_US
dc.subjectearly sensory processingen_US
dc.titleVisual processing deficits in patients with schizophrenia spectrum and bipolar disorders and associations with psychotic symptoms, and intellectual abilitiesen_US
dc.title.alternativeVisual processing deficits in patients with schizophrenia spectrum and bipolar disorders and associations with psychotic symptoms, and intellectual abilitiesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume9en_US
dc.source.journalHeliyonen_US
dc.source.issue2en_US
dc.identifier.doi10.1016/j.heliyon.2023.e13354
dc.identifier.cristin2129196
dc.source.articlenumbere13354en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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