医学
病理生理学
内科学
病因学
疾病
小RNA
肿瘤科
生物标志物
疾病严重程度
病例对照研究
转化生长因子
联想(心理学)
脑源性神经营养因子
炎症
BETA(编程语言)
年轻人
发病机制
共病
转化生长因子β
知情同意
作者
Sinan ALTUNÖZ,Nazan Dolapoglu,Ozgur Baykan,Hilmi Bolat,Ayla Solmaz Avcikurt,Tunay Karlidere,Sinan ALTUNÖZ,Nazan Dolapoglu,Ozgur Baykan,Hilmi Bolat,Ayla Solmaz Avcikurt,Tunay Karlidere
摘要
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 (r s = −0.220, p = 0.045) and disease duration (r s = −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 (r s = 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI