Elevated serum calprotectin levels in major depressive disorder: no evidence of association with s100a9 rs3014866 polymorphism

dc.authorid0000-0001-8551-6900
dc.authorid0000-0002-1521-7152
dc.contributor.authorAkbaş, Furkan
dc.contributor.authorBaykan, Özgur
dc.contributor.authorAvcıkurt , Ayla Solmaz
dc.contributor.authorBaykan, Hayriye
dc.date.accessioned2026-09-16T10:55:42Z
dc.date.issued2026
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü
dc.description.abstractBackground Major depressive disorder (MDD) has been increasingly associated with low-grade inflammation, with neutrophils playing a central role. Calprotectin is a mainly neutrophil-derived inflammatory mediator. We investigated whether serum calprotectin levels are higher in patients with MDD than in healthy controls and whether the S100A9 rs3014866 polymorphism is associated with serum calprotectin levels and with MDD. Methods We enrolled 66 patients with major depressive disorder (MDD) and 54 healthy controls. Depressive symptoms were assessed using the 17-item Hamilton Depression Rating Scale (HAM-D). Fasting venous blood samples were collected to measure serum calprotectin and to genotype the S100A9 rs3014866 polymorphism. Results Serum calprotectin levels were higher in patients with MDD than in healthy controls (2.18±1.33 vs. 1.05±0.55 µg/mL; p<0.001). Serum calprotectin levels were positively correlated with HAM-D scores among patients with MDD (rs=0.314, p=0.010). The S100A9 rs3014866 genotype distribution was in Hardy–Weinberg equilibrium. Genotype and allele frequencies did not differ significantly between patients with MDD and healthy controls, and serum calprotectin levels did not differ significantly across genotype groups under the tested inheritance models. Conclusions These findings suggest that serum calprotectin may reflect inflammatory processes associated with MDD and that its potential role as a biomarker warrants further investigation.
dc.description.sponsorshipBalikesir Universitesi 2023 - 163
dc.identifier.doi10.1186/s12888-026-08161-3
dc.identifier.endpage12
dc.identifier.issn1471-244X
dc.identifier.issue1
dc.identifier.pmid42129725
dc.identifier.scopus2-s2.0-105044119224
dc.identifier.scopusqualityQ1
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.1186/s12888-026-08161-3
dc.identifier.urihttps://hdl.handle.net/20.500.12462/24388
dc.identifier.volume26
dc.identifier.wos001816701900003
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherBMC
dc.relation.ispartofBMC Psychiatry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCalprotectin
dc.subjectMajor Depressive Disorder
dc.subjectrs3014866
dc.subjectGenetic Polymorphism
dc.titleElevated serum calprotectin levels in major depressive disorder: no evidence of association with s100a9 rs3014866 polymorphism
dc.typeArticle

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