Publication:
Role of miRNA Gene Variants (miR-22 and miR-155) as the Factors Affecting Susceptibility to Panic Disorder

dc.authorscopusid55788627100
dc.authorscopusid7801436933
dc.authorscopusid18337953400
dc.authorscopusid57193227350
dc.authorwosidUzun, Ahmet/Iys-2043-2023
dc.authorwosidYeğin, Zeynep/Hlq-7228-2023
dc.authorwosidKoç, Haydar/Jan-8028-2023
dc.contributor.authorYegin, Zeynep
dc.contributor.authorSarisoy, Gokhan
dc.contributor.authorUzun, Ahmet
dc.contributor.authorKoc, Haydar
dc.date.accessioned2025-12-11T00:46:56Z
dc.date.issued2024
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Yegin, Zeynep] Sinop Univ, Vocat Sch Hlth Serv, Med Lab Tech Program, TR-57000 Sinop, Turkiye; [Sarisoy, Gokhan; Uzun, Ahmet] Ondokuz Mayis Univ, Fac Med, Dept Psychiat, Samsun, Turkiye; [Koc, Haydar] Cankiri Karatekin Univ, Fac Sci, Dept Stat, Cankiri, Turkiyeen_US
dc.description.abstractObjective: Variants within genes encoding microRNAs (miRNAs) may alter the expression of both miRNAs and their target genes, thus contributing to the etiology of psychiatric disorders. The involvement of miRNAs in neuronal differentiation and synaptic plasticity supported this hypothesis. We aimed to investigate the links between miR-155 rs767649/miR-22 rs8076112 and the risk of panic disorder (PD) in a sample of Turkish population. Methods: In this experimental study, 134 PD patients and 140 healthy controls were recruited. Genotyping was carried out using Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) method. To evaluate PD phenotypes, Panic Disorder Severity Scale (PDSS) was also administered to patients to clarify possible associations between the scale and risk variants analyzed. Results: The genotype analysis of miR-155 rs767649 did not show an association with PD risk and it was not related to the disease severity. For miR-22 rs8076112 variant, a statistically significant association was determined; CC genotypes were lower in patients compared to controls. Logistic regression analysis proved the highly protective effect (80.4%) of CC genotype against PD (p = 0.041; OR = 0.196, 95% CI = 0.041-0.934). Though its significance in disease liability, miR-22 rs8076112 was not associated with the disease severity. Conclusion: Our findings firstly report the combined analysis of miR-155 rs767649 and miR-22 rs8076112 in PD in terms of both disease susceptibility and severity. These findings await replication in independent cohorts with enrichment of other miRNA gene variants. Thus, certain miRNAs and their target genes involved in the etiology and phenotypes of PD could be enlightened.en_US
dc.description.sponsorshipCankiri Karatekin University Scientific Research Projects Coordination Unit [FF210621B10]en_US
dc.description.sponsorship<BOLD> <black square> Funding _ </BOLD> This work was supported by Cankiri Karatekin University Scientific Research Projects Coordination Unit. Project Number: FF210621B10.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.9758/cpn.24.1201
dc.identifier.endpage661en_US
dc.identifier.issn1738-1088
dc.identifier.issn2093-4327
dc.identifier.issue4en_US
dc.identifier.pmid39420612
dc.identifier.scopus2-s2.0-85207632922
dc.identifier.scopusqualityQ2
dc.identifier.startpage655en_US
dc.identifier.urihttps://doi.org/10.9758/cpn.24.1201
dc.identifier.urihttps://hdl.handle.net/20.500.12712/39189
dc.identifier.volume22en_US
dc.identifier.wosWOS:001398333400011
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherKorean Coll Neuropsychopharmacologyen_US
dc.relation.ispartofClinical Psychopharmacology and Neuroscienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPanic Disorderen_US
dc.subjectMicroRNAen_US
dc.subjectGenetic Associationen_US
dc.subjectmiR-22en_US
dc.subjectmiR-155en_US
dc.subjectPanic Disorder Severity Scaleen_US
dc.titleRole of miRNA Gene Variants (miR-22 and miR-155) as the Factors Affecting Susceptibility to Panic Disorderen_US
dc.typeArticleen_US
dspace.entity.typePublication

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