Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30152
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dc.contributor.authorAydın, Orkun-
dc.contributor.authorKocabaş, Tuğba-
dc.contributor.authorTaştan, İsmail-
dc.contributor.authorOnur, Ece-
dc.contributor.authorAydemir, Ömer-
dc.contributor.authorEsen Danacı, Ayten-
dc.date.accessioned2022-12-29T05:57:14Z-
dc.date.available2022-12-29T05:57:14Z-
dc.date.issued2020-07-14-
dc.identifier.citationAydın, O. vd. (2020). "Examination of plasma zonulin levels in bipolar I disorder: A case-control study with follow-up". Journal Of Neural Transmission, 127(10), 1419-1426.en_US
dc.identifier.issn0300-9564-
dc.identifier.issn1435-1463-
dc.identifier.urihttps://doi.org/10.1007/s00702-020-02234-7-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00702-020-02234-7-
dc.identifier.urihttp://hdl.handle.net/11452/30152-
dc.description.abstractThere is an accumulation in studies which strive to reveal zonulin's potential role in mental disorders. To date, one cross-sectional recent study examined zonulin in patients with bipolar disorders (BDs); however, its role still remains vague due to high fluctuation. Our aims are to determine plasma zonulin levels in exacerbation and treatment response periods, and to examine the associations between zonulin and symptom severity in BD. 30 patients with BD type I and 29 healthy controls participated in the current study. Socio-demographic form, Young Mania Rating Scale (YMRS), and Hamilton Depression Rating Scale (HAM-D) were administered. Enzyme-linked immune assay (ELISA) method was used to measure the plasma zonulin levels of the participants. The groups did not differ in plasma zonulin-level comparisons. Plasma zonulin did not alter between the exacerbation and treatment response periods of the patients. Besides, no associations were found between plasma zonulin-level and disease symptoms. Intestinal barrier integrity was not found to be altered among patients with BD type I. The lack of alterations in plasma zonulin level between different periods may be attributable to several factors. One possible factor might be the ELISA method which can detect other proteins (e.g., properdin) rather than zonulin. Therefore, it might fail to indicate direct observation of intestinal permeability. However, future study designs with more accurate estimation of zonulin in a larger sample may provide a different perspective on intestinal permeability's possible role in BD etiology.en_US
dc.description.sponsorshipCelal Bayar Üniversitesi (2018-225)tr_TR
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectZonulinen_US
dc.subjectBipolar disorderen_US
dc.subjectHaptoglobinen_US
dc.subjectAutoimmuneen_US
dc.subjectInflammationen_US
dc.subjectSymptom severityen_US
dc.subjectAutism spectrum disordersen_US
dc.subjectIntestinal permeabilityen_US
dc.subjectTight junctionsen_US
dc.subjectGut permeabilityen_US
dc.subjectCeliac-diseaseen_US
dc.subjectSerum zonulinen_US
dc.subjectRating-scaleen_US
dc.subjectSchizophreniaen_US
dc.subjectPathogenesisen_US
dc.subjectReliabilityen_US
dc.subjectNeurosciences & neurologyen_US
dc.subject.meshBipolar disorderen_US
dc.subject.meshCase-control studiesen_US
dc.subject.meshCross-sectional studiesen_US
dc.subject.meshFollow-up studiesen_US
dc.subject.meshHaptoglobinsen_US
dc.subject.meshHumansen_US
dc.subject.meshProtein precursorsen_US
dc.titleExamination of plasma zonulin levels in bipolar I disorder: A case-control study with follow-upen_US
dc.typeArticleen_US
dc.identifier.wos000551056000001tr_TR
dc.identifier.scopus2-s2.0-85088303775tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-1092-8254tr_TR
dc.identifier.startpage1419tr_TR
dc.identifier.endpage1426tr_TR
dc.identifier.volume127tr_TR
dc.identifier.issue10tr_TR
dc.relation.journalJournal Of Neural Transmissionen_US
dc.contributor.buuauthorSarandöl, Aslı-
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed32696242tr_TR
dc.subject.wosClinical neurologyen_US
dc.subject.wosNeurosciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2 (Clinical neurology)en_US
dc.wos.quartileQ3 (Neurosciences)en_US
dc.contributor.scopusid14020405100tr_TR
dc.subject.scopusZonulin; Enteric Coating; Gastrointestinal Diseasesen_US
dc.subject.emtreeProteinen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeZonulinen_US
dc.subject.emtreeHaptoglobinen_US
dc.subject.emtreeProtein precursoren_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBipolar I disorderen_US
dc.subject.emtreeBody massen_US
dc.subject.emtreeCase control studyen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeComparative studyen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCross-sectional studyen_US
dc.subject.emtreeDisease durationen_US
dc.subject.emtreeDisease exacerbationen_US
dc.subject.emtreeDisease severityen_US
dc.subject.emtreeEnzyme linked immunosorbent assayen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeHamilton depression rating scaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHypochondriasisen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProtein blood levelen_US
dc.subject.emtreeTobacco useen_US
dc.subject.emtreeTreatment durationen_US
dc.subject.emtreeTreatment responseen_US
dc.subject.emtreeYoung mania rating scaleen_US
dc.subject.emtreeBipolar disorderen_US
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