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dc.contributor.authorSæther, Linn Sofie
dc.contributor.authorUeland, Thor
dc.contributor.authorHaatveit, Beathe
dc.contributor.authorVaskinn, Anja
dc.contributor.authorFlaaten, Camilla Bärthel
dc.contributor.authorMohn, Hanne Christine
dc.contributor.authorOrmerod, Monica Bettina E. Greenwood
dc.contributor.authorAukrust, Pål
dc.contributor.authorMelle, Ingrid
dc.contributor.authorSteen, Nils Eiel
dc.contributor.authorAndreassen, Ole
dc.contributor.authorUeland, Torill
dc.date.accessioned2024-11-13T12:57:39Z
dc.date.available2024-11-13T12:57:39Z
dc.date.issued2024-10-02
dc.description.abstractBackground - While inflammation is associated with cognitive impairment in severe mental illnesses (SMI), there is substantial heterogeneity and evidence of transdiagnostic subgroups across schizophrenia (SZ) and bipolar (BD) spectrum disorders. There is however, limited knowledge about the longitudinal course of this relationship.<p> <p>Methods - Systemic inflammation (C-Reactive Protein, CRP) and cognition (nine cognitive domains) was measured from baseline to 1 year follow-up in first treatment SZ and BD (n = 221), and healthy controls (HC, n = 220). Linear mixed models were used to evaluate longitudinal changes separately in CRP and cognitive domains specific to diagnostic status (SZ, BD, HC). Hierarchical clustering was applied on the entire sample to investigate the longitudinal course of transdiagnostic inflammatory-cognitive subgroups.<p> <p>Results - There were no case-control differences or change in CRP from baseline to follow-up. We confirm previous observations of case-control differences in cognition at both time-points and domain specific stability/improvement over time regardless of diagnostic status. We identified transdiagnostic inflammatory-cognitive subgroups at baseline with differing demographics and clinical severity. Despite improvement in cognition, symptoms and functioning, the higher inflammation – lower cognition subgroup (75% SZ; 48% BD; 38% HC) had sustained inflammation and lower cognition, more symptoms, and lower functioning (SMI only) at follow-up. This was in comparison to a lower inflammation – higher cognition subgroup (25% SZ, 52% BD, 62% HC), where SMI participants showed cognitive functioning at HC level with a positive clinical course.<p> <p>Conclusions - Our findings support heterogenous and transdiagnostic inflammatory-cognitive subgroups that are stable over time, and may benefit from targeted interventions.en_US
dc.identifier.citationSæther, Ueland, Haatveit, Vaskinn, Flaaten, Mohn, Ormerod, Aukrust, Melle, Steen, Andreassen, Ueland. Longitudinal course of inflammatory-cognitive subgroups across first treatment severe mental illness and healthy controls. Psychological Medicine. 2024
dc.identifier.cristinIDFRIDAID 2313328
dc.identifier.doi10.1017/S003329172400206X
dc.identifier.issn0033-2917
dc.identifier.issn1469-8978
dc.identifier.urihttps://hdl.handle.net/10037/35692
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.relation.journalPsychological Medicine
dc.rights.holderCopyright 2024 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleLongitudinal course of inflammatory-cognitive subgroups across first treatment severe mental illness and healthy controlsen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)