Department of Psychiatry, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Psychiatry, Affiliated Nanjing Brain Hospital, Nanjing Medical University, Nanjing, China.
J Psychopharmacol. 2021 Jan;35(1):23-30. doi: 10.1177/0269881120959617. Epub 2020 Dec 4.
Disturbances of microRNA-195 have been implicated in the pathogenesis of schizophrenia. However, microRNA-195 levels in schizophrenia are controversial.
To the best of our knowledge, this is the first study to examine microRNA-195 levels in untreated schizophrenia patients and their relationship to olanzapine response.
We recruited 81 untreated schizophrenia patients and 96 healthy controls. The patients received 2 months olanzapine treatment. MicroRNA-195 levels in peripheral blood mononuclear cells were measured using quantitative real-time polymerase chain reaction testing. Psychiatric symptoms were assessed using the Positive and Negative Syndrome Scale.
No significant differences in microRNA-195 levels were found between patients and healthy controls ( 0.05). Olanzapine significantly reduced microRNA-195 levels after 2 months treatment ( 0.003). Interestingly, microRNA-195 levels decreased significantly in responders ( 0.010), but not in non-responders ( 0.05). Both baseline microRNA-195 levels ( 0.027, 0.030) and the reduction rate of microRNA-195 levels ( 0.034, 0.044) were positively associated with the reduction rate of Positive and Negative Syndrome Scale total score and general psychopathological subscale score. Multiple stepwise regression analysis revealed that baseline microRNA-195 level was an independent contributor to the reduction in Positive and Negative Syndrome Scale total score and the general psychopathological subscale score ( 0.018, 0.030). Finally, logistic regression analysis suggested that baseline microRNA-195 level can serve as a biomarker for response to olanzapine ( 0.037).
Our data indicate that microRNA-195 level may predict symptomatic improvement and olanzapine response in schizophrenia patients, suggesting that microRNA-195 should be considered as a potential therapeutic target for antipsychotics.
miRNA-195 的紊乱与精神分裂症的发病机制有关。然而,精神分裂症患者的 miRNA-195 水平存在争议。
据我们所知,这是第一项研究,旨在检查未经治疗的精神分裂症患者的 miRNA-195 水平及其与奥氮平反应的关系。
我们招募了 81 名未经治疗的精神分裂症患者和 96 名健康对照者。患者接受了 2 个月的奥氮平治疗。采用实时定量聚合酶链反应检测外周血单个核细胞中的 miRNA-195 水平。采用阳性和阴性综合征量表评估精神症状。
患者和健康对照组之间的 miRNA-195 水平无显著差异(0.05)。奥氮平治疗 2 个月后,miRNA-195 水平显著降低(0.003)。有趣的是,应答者的 miRNA-195 水平显著降低(0.010),而非应答者的 miRNA-195 水平无显著变化(0.05)。基线 miRNA-195 水平(0.027,0.030)和 miRNA-195 水平降低率(0.034,0.044)与阳性和阴性综合征量表总分及一般精神病理子量表评分的降低率呈正相关。多元逐步回归分析显示,基线 miRNA-195 水平是阳性和阴性综合征量表总分及一般精神病理子量表评分降低的独立贡献因素(0.018,0.030)。最后,逻辑回归分析表明,基线 miRNA-195 水平可以作为奥氮平反应的生物标志物(0.037)。
我们的数据表明,miRNA-195 水平可能预测精神分裂症患者的症状改善和奥氮平反应,表明 miRNA-195 可被视为抗精神病药物的潜在治疗靶点。