Could transforming growth factor beta and target microrna dysregulation serve as biomarkers of symptom severity in patients with obsessive‐compulsive disorder?
| dc.authorid | 0000-0003-1400-7580 | |
| dc.authorid | 0000-0001-8551-6900 | |
| dc.authorid | 0000-0001-6574-8149 | |
| dc.authorid | 0000-0002-1521-7152 | |
| dc.authorid | 0000-0003-2143-0651 | |
| dc.contributor.author | Altunöz, Sinan | |
| dc.contributor.author | Dolapoğlu, Nazan | |
| dc.contributor.author | Baykan, Özgür | |
| dc.contributor.author | Bolat, Hilmi | |
| dc.contributor.author | Avcıkurt, Ayla Solmaz | |
| dc.contributor.author | Karlıdere, Tunay | |
| dc.date.accessioned | 2026-03-13T11:21:19Z | |
| dc.date.issued | 2025 | |
| dc.department | Fakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | |
| dc.description.abstract | Introduction: This study investigated the regulation of miRNA-132-3p on TGF-β levels and its association with OCD severity. We hypothesized that miRNA-132-3p and TGF-β influence OCD aetiology and severity, with their levels correlating with disease severity. Methods: The study included 48 OCD patients diagnosed via SCID-5-CV per DSM-V and 48 matched healthy controls. Blood samples were analysed for miRNA-132-3p and TGF-β using RT-PCR and ELISA. Participants completed Y-BOCS, symptom list, HAMA, HAMD, consent and sociodemographic forms. Results: OCD patients had significantly lower TGF-β levels (p=0.008), negatively correlating with Y-BOCS scores (rs=−0.220, p=0.045) and disease duration (rs=−0.473, p=0.002). miRNA-132-3p levels were 1.92 times higher in OCD patients (p=0.003), positively correlating with Y-BOCS scores (rs=0.208, p=0.045). Conclusions: Altered TGF-β and miRNA-132-3p levels may contribute to OCD pathophysiology by affecting BDNF regulation, inflammatory responses (Th1/Th2, Th17/Treg balance) and synaptic plasticity-related genes. | |
| dc.identifier.doi | 10.1002/jdn.70070 | |
| dc.identifier.endpage | 6 | |
| dc.identifier.issn | 0736-5748 | |
| dc.identifier.issue | 7 | |
| dc.identifier.pmid | 41239944 | |
| dc.identifier.scopus | 2-s2.0-105021812489 | |
| dc.identifier.scopusquality | Q4 | |
| dc.identifier.startpage | 1 | |
| dc.identifier.uri | https://doi.org/10.1002/jdn.70070 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/23490 | |
| dc.identifier.volume | 85 | |
| dc.identifier.wos | 001626865900010 | |
| dc.identifier.wosquality | Q4 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Wiley | |
| dc.relation.ispartof | International Journal of Developmental Neuroscience | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Mirna | |
| dc.subject | Obsessive-Compulsive Disorder | |
| dc.subject | TGF-Β | |
| dc.title | Could transforming growth factor beta and target microrna dysregulation serve as biomarkers of symptom severity in patients with obsessive‐compulsive disorder? | |
| dc.type | Article |












