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dc.contributor.authorGroven, Nina
dc.contributor.authorFors, Egil Andreas
dc.contributor.authorIversen, Valentina Cabral
dc.contributor.authorWhite, Linda Rosemary
dc.contributor.authorReitan, Solveig Merete Klæbo
dc.date.accessioned2019-02-18T14:44:08Z
dc.date.available2019-02-18T14:44:08Z
dc.date.created2018-08-03T15:29:01Z
dc.date.issued2018
dc.identifier.citationNordic Journal of Psychiatry. 2018, 1-6.nb_NO
dc.identifier.issn0803-9488
dc.identifier.urihttp://hdl.handle.net/11250/2586046
dc.description.abstractPurpose: The reports regarding the status of the immune system in patients with chronic fatigue syndrome/myalgic encephalopathy (CFS/ME) have been inconclusive. We approached this question by comparing a strictly defined group of CFS/ME outpatients to healthy control individuals, and thereafter studied cytokines in subgroups with various psychiatric symptoms. Materials and methods: Twenty patients diagnosed with CFS/ME according to the Fukuda criteria and 20 age- and sex-matched healthy controls were enrolled in the study. Plasma was analysed by ELISA for levels of the cytokines TNF-α, IL-4, IL-6 and IL-10. Participants also answered questionnaires regarding health in general, and psychiatric symptoms in detail. Results: Increased plasma levels of TNF-α in CFS/ME patients almost reached significance compared to healthy controls (p = .056). When studying the CFS/ME and control groups separately, there was a significant correlation between TNF-α and The Hospital Anxiety and Depression Scale (HADS) depressive symptoms in controls only, not in the CFS/ME group. A correlation between IL-10 and psychoticism was found in both groups, whereas the correlation for somatisation was seen only in the CFS/ME group. When looking at the total population, there was a significant correlation between TNF-α and both the HADS depressive symptoms and the SCL-90-R cluster somatisation. Also, there was a significant association between IL-10 and the SCL-90-R cluster somatisation when analyzing the cohort (patients and controls together). Conclusions: These findings indicate that immune activity in CFS/ME patients deviates from that of healthy controls, which implies potential pathogenic mechanisms and possible therapeutic approaches to CFS/ME. More comprehensive studies should be carried out on defined CFS/ME subgroups.nb_NO
dc.language.isoengnb_NO
dc.publisherTaylor & Francisnb_NO
dc.relation.urihttps://www.tandfonline.com/doi/full/10.1080/08039488.2018.1493747
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.subjectNevropsykiatrinb_NO
dc.subjectNeuropsychiatrynb_NO
dc.titleAssociation between cytokines and psychiatric symptoms in chronic fatigue syndrome and healthy controlsnb_NO
dc.title.alternativeAssociation between cytokines and psychiatric symptoms in chronic fatigue syndrome and healthy controlsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.subject.nsiVDP::Basale medisinske, odontologiske og veterinærmedisinske fag: 710nb_NO
dc.subject.nsiVDP::Basic medical, dental and veterinary sciences: 710nb_NO
dc.source.pagenumber1-6nb_NO
dc.source.volume72nb_NO
dc.source.journalNordic Journal of Psychiatrynb_NO
dc.source.issue8nb_NO
dc.identifier.doi10.1080/08039488.2018.1493747
dc.identifier.cristin1599690
dc.description.localcode(C) 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.nb_NO
cristin.unitcode194,65,35,0
cristin.unitcode194,65,20,0
cristin.unitcode194,65,30,0
cristin.unitnameInstitutt for psykisk helse
cristin.unitnameInstitutt for samfunnsmedisin og sykepleie
cristin.unitnameInstitutt for nevromedisin og bevegelsesvitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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