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dc.contributor.authorSchou, Morten Brix
dc.contributor.authorSæther, Sverre Georg
dc.contributor.authorBorowski, K
dc.contributor.authorTeegen, B
dc.contributor.authorKondziella, Daniel
dc.contributor.authorStoecker, W
dc.contributor.authorVaaler, Arne Einar
dc.contributor.authorReitan, Solveig Merete Klæbo
dc.date.accessioned2019-01-21T08:24:32Z
dc.date.available2019-01-21T08:24:32Z
dc.date.created2016-09-28T09:38:17Z
dc.date.issued2016
dc.identifier.citationPsychological Medicine. 2016, 46 (16), 3303-3313.nb_NO
dc.identifier.issn0033-2917
dc.identifier.urihttp://hdl.handle.net/11250/2581370
dc.description.abstractBackground Autoimmune encephalitis associated with anti-neuronal antibodies may be challenging to distinguish from primary psychiatric disorders. The significance of anti-neuronal antibodies in psychiatric patients without clear evidence of autoimmune encephalitis is unknown. We investigated the serum prevalence of six anti-neuronal autoantibodies in a cohort of unselected patients admitted to acute psychiatric care. Method Serum was drawn from 925 patients admitted to acute psychiatric in-patient care. Psychiatric diagnoses were set according to International Classification of Diseases (ICD)-10 criteria. Antibody analysis was performed with an indirect immunofluorescence test for N-methyl d-aspartate receptor (NMDAR) antibodies and five other anti-neuronal autoantibodies of the immunoglobulin (Ig) classes IgA, IgG and IgM isotype. Results Anti-neuronal autoantibodies were found in 11.6% of patients: NMDAR antibodies in 7.6%, contactin-associated protein-like 2 (CASPR2) antibodies in 2.5%, glutamic acid decarboxylase-65 (GAD65) antibodies in 1.9%, and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antibodies in 0.1%. Leucine-rich glioma-inactivated protein-1 (LGI1) and γ-aminobutyric acid B (GABAB) receptor antibodies were not detected. NMDAR antibodies of class IgG were present in five patients only (0.5%). NMDAR antibodies of all Ig classes were equally prevalent in patients with and without psychosis. There were no significant differences in antibody prevalence in the different diagnostic categories, except for a higher odds ratio of being NMDAR antibody positive for patients without a specific psychiatric diagnosis. Conclusions NMDAR IgG autoantibodies, which are known to be strongly associated with anti-NMDAR encephalitis, were rarely found. CASPR2 and GAD65 antibodies were more frequently encountered in the present study than previously reported. Further research on the clinical significance of anti-neuronal autoantibodies in patients with acute psychiatric symptoms is needed.nb_NO
dc.language.isoengnb_NO
dc.publisherCambridge University Pressnb_NO
dc.titlePrevalence of serum anti-neuronal autoantibodies in patients admitted to acute psychiatric carenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber3303-3313nb_NO
dc.source.volume46nb_NO
dc.source.journalPsychological Medicinenb_NO
dc.source.issue16nb_NO
dc.identifier.doi10.1017/S0033291716002038
dc.identifier.cristin1386713
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2016 by Cambridge University Pressnb_NO
cristin.unitcode194,65,30,0
cristin.unitcode194,65,35,0
cristin.unitnameInstitutt for nevromedisin og bevegelsesvitenskap
cristin.unitnameInstitutt for psykisk helse
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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