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dc.date.accessioned2021-12-18T18:18:12Z
dc.date.available2021-12-18T18:18:12Z
dc.date.created2021-11-26T18:27:05Z
dc.date.issued2021
dc.identifier.citationVærnes, Tor Gunnar Røssberg, Jan Ivar Melle, Ingrid Nelson, Barnaby Romm, Kristin Lie Møller, Paul . Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study. European Archives of Psychiatry and Clinical Neuroscience. 2021, 1-13
dc.identifier.urihttp://hdl.handle.net/10852/89638
dc.description.abstractAbstract Basic self-disturbance (BSD) has been proposed as a driver of symptom development in schizophrenia spectrum disorders (SSDs). In a one-year follow-up of 32 patients (15–30 years) at putative risk for psychosis, we investigated trajectories of BSD levels from baseline to follow-up, and associations between clinical characteristics at baseline and follow-up, including follow-up levels of BSD (assessed with the EASE). Clinical high risk (CHR) for psychosis status and symptom severity were assessed with the SIPS/SOPS scales and also according to the cognitive basic symptoms high-risk criteria (COGDIS). DSM-IV diagnoses, functioning and other clinical characteristics were assessed with standard clinical instruments. Higher severity of negative symptoms and meeting COGDIS criteria at baseline were associated with higher BSD levels at follow-up. All measured at follow-up, higher BSD levels correlated with higher severity of positive, negative, disorganization and general symptoms, and with a lower level of global functioning. We found higher BSD levels at follow-up in subjects with schizotypal personality disorder (SPD) at baseline ( n  = 5) and in SSDs at follow-up ( n  = 12, including nine with SPD). Mean BSD levels decreased significantly from baseline to follow-up, but individual trajectories varied considerably. Increased BSD levels were associated with higher baseline BSD levels, non-remission of positive symptoms and functional decline. Overall, the current study indicates that subgroups in the CHR population with a higher risk of non-remission or deterioration may be identified by supplementing CHR criteria with assessment of BSD and negative symptoms.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleBasic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
dc.typeJournal article
dc.creator.authorVærnes, Tor Gunnar
dc.creator.authorRøssberg, Jan Ivar
dc.creator.authorMelle, Ingrid
dc.creator.authorNelson, Barnaby
dc.creator.authorRomm, Kristin Lie
dc.creator.authorMøller, Paul
cristin.unitcode185,53,10,14
cristin.unitnameEnhet voksenpsykiatri
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1960026
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=European Archives of Psychiatry and Clinical Neuroscience&rft.volume=&rft.spage=1&rft.date=2021
dc.identifier.jtitleEuropean Archives of Psychiatry and Clinical Neuroscience
dc.identifier.startpage1
dc.identifier.endpage13
dc.identifier.doihttps://doi.org/10.1007/s00406-021-01349-6
dc.identifier.urnURN:NBN:no-92251
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0940-1334
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/89638/1/Basic%2Bself-disturbance%2Btrajectories%2Bin%2Bclinical%2Bhigh%2Brisk%2Bfor%2Bpsychosis%253B%2Ba%2Bone-year%2Bfollow-up%2Bstudy.pdf
dc.type.versionPublishedVersion


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