Bipolar and major depressive disorders: associations with serum zonulin levels and rs2070937 polymorphism

dc.authorid0000-0001-8551-6900
dc.authorid0000-0002-1521-7152
dc.authorid0000-0002-3288-2269
dc.authorid0000-0002-3837-250X
dc.contributor.authorBaykan,Özgür
dc.contributor.authorAkbaş, Furkan
dc.contributor.authorAvcıkurt,Ayla Solmaz
dc.contributor.authorBaykan, Hayriye
dc.date.accessioned2026-03-06T06:30:48Z
dc.date.issued2025
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü
dc.description.abstractBackground The underlying pathophysiology of bipolar disorder and major depressive disorder is not fully understood. Inflammation is increasingly recognized as a contributing factor. The gut plays a central role in this process. Increased intestinal permeability, which promotes inflammation, is regulated by tight junctions and influenced by the zonulin protein. This mechanism has been linked to both inflammatory and psychiatric disorders. This study investigates differences in serum zonulin levels and the rs2070937 genetic polymorphism among patients with bipolar disorder, major depressive disorder, and healthy controls. Methods A total of 47 patients with bipolar disorder, 56 patients with major depressive disorder, and 51 healthy controls were enrolled. Manic and depressive symptom severity were assessed with the Young Mania Rating Scale and the Hamilton Depression Rating Scale. Venous blood samples were collected from all participants to evaluate serum zonulin levels and to perform genotyping of the rs2070937 polymorphism. Results Serum zonulin levels were significantly higher in patients with bipolar disorder compared to healthy controls (padj = 0.012), and in patients with major depressive disorder compared to healthy controls (padj < 0.001). No significant differences were observed between the bipolar disorder and major depressive disorder groups. Analysis of rs2070937 genotypes (AA, AG, GG) revealed no significant differences in serum zonulin levels within genotype groups. Furthermore, the distribution of genotypes did not differ significantly among the bipolar disorder, major depressive disorder, and healthy control groups. Conclusions Our findings suggest that increased gut permeability may contribute to the pathophysiology of bipolar disorder and major depressive disorder. Recognizing the role of the gut–brain axis in mood disorders could facilitate earlier screening and support the development of personalized treatment approaches.
dc.identifier.doi10.1186/s12888-025-07548-y
dc.identifier.endpage12
dc.identifier.issn1472-244X
dc.identifier.issue1
dc.identifier.pmid41233834
dc.identifier.scopus2-s2.0-105021545984
dc.identifier.scopusqualityQ1
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.1186/s12888-025-07548-y
dc.identifier.urihttps://hdl.handle.net/20.500.12462/23374
dc.identifier.volume25
dc.identifier.wos001626461700004
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherBMC
dc.relation.ispartofBMC Psychiatry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectZonulin
dc.subjectBipolar Disorder
dc.subjectMajor Depressive Disorder
dc.subjectGut–Brain Axis
dc.subjectRs2070937
dc.subjectGenetic Polymorphism
dc.titleBipolar and major depressive disorders: associations with serum zonulin levels and rs2070937 polymorphism
dc.typeArticle

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