Publication:
Estrogen Receptor 1 Gene RS22346939 and RS9340799 Variants are Associated with Major Depressive Disorder and Its Clinical Features

dc.authorscopusid57195102884
dc.authorscopusid55820023600
dc.authorscopusid24781203900
dc.authorscopusid57077999200
dc.authorscopusid12805499100
dc.authorwosidKarakus, Nevin/Aab-1587-2022
dc.authorwosidYigit, Serbulent/Abb-9572-2020
dc.authorwosidNursal, Ayse/Abg-7404-2021
dc.contributor.authorOzsoy, Filiz
dc.contributor.authorNursal, Ayse F.
dc.contributor.authorKarakus, Nevin
dc.contributor.authorDemir, Meral O.
dc.contributor.authorYigit, Serbulent
dc.contributor.authorIDKarakus, Nevin/0000-0002-1916-7471
dc.contributor.authorIDÖzsoy, Fi̇li̇z/0000-0002-5198-8827
dc.date.accessioned2025-12-11T01:20:42Z
dc.date.issued2021
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ozsoy, Filiz] Tokat State Hosp, Dept Psychiat, Tokat, Turkey; [Nursal, Ayse F.] Hitit Univ, Fac Med, Dept Med Genet, Corum, Turkey; [Karakus, Nevin] Tokat Gaziosmanpasa Univ, Fac Med, Dept Med Biol, Tokat, Turkey; [Demir, Meral O.] Dr Cevdet Aykan Mental & Neurol Dis Hosp, Dept Psychiat, Tokat, Turkey; [Yigit, Serbulent] Ondokuz Mayis Univ, Fac Vet, Dept Genet, Samsun, Turkeyen_US
dc.descriptionKarakus, Nevin/0000-0002-1916-7471; Özsoy, Fi̇li̇z/0000-0002-5198-8827;en_US
dc.description.abstractObjective: Major Depressive Disorder (MDD) is a major health problem worldwide. Estrogen interacts with the central nervous system and has been shown to affect anxiety and depressive behavior. Estrogen mediates its effects by connecting its receptors, estrogen receptors 1 and 2. The purpose of this case-control study was to clarify the association between MDD risk and estrogen receptor 1 (ESR1) gene variants. Methods: This study included 245 individuals (125 MDD patients and 120 healthy controls). Polymerase Chain Reaction (PCR) and Restriction Fragment Length Polymorphism (RFLP) technics were used for genotypingESR1XbaII (rs9340799) and PvuII (rs22346939) variants. Results: There were statistically significant differences between the groups in terms of genotype frequencies of the ESR1PvuII (-397 T > C) variant (p = 0.049) but not for the XbaII (-351 A > G) variant (p > 0.05). However, a correlation was observed between MDD and ESR1XbaII variant after male participants were excluded (p = 0.028). Also, the high pain score of MDD patients was associated with the ESR1PvuII variant, especially in female patients (p = 0.021). According to the results of combined genotype analysis, AA-TC combined genotype was correlated with a decreased risk in patients with MDD compared to controls (p = 0.016), while the combined genotype of GGCC was associated with increased risk in the patients with MDD compared to controls (p = 0.042). Conclusion: The two ESR1 variants were associated with MDD risk and its features in both individual and combined forms.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.2174/1567202618666210531122239
dc.identifier.endpage19en_US
dc.identifier.issn1567-2026
dc.identifier.issn1875-5739
dc.identifier.issue1en_US
dc.identifier.pmid34060989
dc.identifier.scopus2-s2.0-85115040289
dc.identifier.scopusqualityQ4
dc.identifier.startpage12en_US
dc.identifier.urihttps://doi.org/10.2174/1567202618666210531122239
dc.identifier.urihttps://hdl.handle.net/20.500.12712/43062
dc.identifier.volume18en_US
dc.identifier.wosWOS:000687885000003
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherBentham Science Publishing Ltden_US
dc.relation.ispartofCurrent Neurovascular Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEstrogen Receptor 1en_US
dc.subjectMajor Depressive Disorderen_US
dc.subjectVarianten_US
dc.subjectrs22346939en_US
dc.subjectrs9340799en_US
dc.subjectPCR-RFLPen_US
dc.titleEstrogen Receptor 1 Gene RS22346939 and RS9340799 Variants are Associated with Major Depressive Disorder and Its Clinical Featuresen_US
dc.typeArticleen_US
dspace.entity.typePublication

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