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首页> 外文期刊>Central European Journal of Biology >Aberrant expression of microRNA-132-3p and microRNA-146a-5p in Parkinson’s disease patients
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Aberrant expression of microRNA-132-3p and microRNA-146a-5p in Parkinson’s disease patients

机译:MicroRNA-132-3P和MicroRNA-146A-5P在帕金森病患者中的异常表达

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摘要

Parkinson’s disease (PD) is an age-related neurodegenerative disorder which is assessed based on the motor symptoms. A number of microRNAs (miRNAs) are dysregulated and involved in the pathogenesis or development of PD. However, no confirmed markers are used for the early detection of PD. The present study aimed to elucidate the potential two miRNAs (miR-132-3p and miR-146-5p) as novel markers for early PD diagnosis. In the present study, the expression levels of miR-132-3p and miR-146-5p in serum samples from 82 patients with PD and 44 healthy volunteers were measured by reverse transcription-quantitative polymerase chain reaction. Furthermore, the correlation analysis was performed between aberrant miRNAs and Braak staging, Part V of the Unified Parkinson’s Disease Rating Scale (UPDRS-V; the modified Hoehn and Yahr staging of PD) and Part III of the UPDRS-III. Subsequently, the receiver–operating characteristic (ROC) curve results of miR-132-3p and miR-146-5p from healthy volunteers for PD prediction and from severe PD patients were assessed. From the results it was observed that miR-132-3p and miR-146a-5p expressions were significantly decreased in the serum samples of patients with PD compared to those in the healthy volunteers. Moreover, the expressions of miR-132-3p and miR-146a-5p showed a dramatic decrease in severe PD patients as compared to the normal PD patients. Meanwhile, miR-132-3p and miR-146-5p expressions were negatively correlated with Braak staging ( r = ?0.45, P 0.0001; r = ?0.51, P 0.0001), UPDRS-III ( r = ?0.55, P 0.0001; r = ?0.51, P 0.0001) and UPDRS-V scores ( r = ? 0.46, P 0.0001; r = ?0.45, P 0.0001) in PD patients. The area under the curve (AUC) results of miR-132-3p and miR-146a-5p in discriminating PD patients from the healthy controls were 0.7325 (95% CI = 0.6400–0.8251) and 0.7295 (95% CI = 0.3658–0.8232). Moreover, the AUC results of miR-132-3p and miR-146-5p concerning discriminating severe PD patients from normal PD patients were 0.8175 (95% CI = 0.7229–0.9121) and 0.7921 (95% CI = 0.6937–0.8905). In other words, both miR-132-3p and miR-146a-5p may function as promising biomarkers for early diagnosis of PD.
机译:帕金森病(PD)是一种与年龄相关的神经变性障碍,其基于运动症状评估。多种微小RORNA(miRNA)进行了诱导并参与PD的发病机制或发育。然而,没有确认的标记用于早期检测PD。本研究旨在阐明潜在的两种miRNA(miR-132-3p和miR-146-5p)作为早期Pd诊断的新标志物。在本研究中,通过逆转录定量聚合酶链反应测量来自82例PD和44例健康志愿者的血清样品中miR-132-3p和miR-146-5p的表达水平。此外,在异常miRNA和BRAAK分期之间进行相关分析,统一帕金森病评级规模的V部分v(UPDRS-V; PD的改性Hoehn和Yahr阶段)和UPDRS-III的第III部分。随后,评估来自HD预测的健康志愿者和来自严重PD患者的MIR-132-3P和MIR-146-5P的接收器操作特征(ROC)曲线结果。从结果观察到,与健康志愿者的患者患者的血清样本中,MIR-132-3P和MIR-146A-5P表达显着降低。此外,与正常的PD患者相比,miR-132-3p和miR-146a-5p的表达显示出严重的PD患者的显着降低。同时,miR-132-3p和miR-146-5p表达与braak分段呈负相关(r = 0.45,p <0.0001; r =Δ0.51,p <0.0001),updrs-III(r =?0.55,p <0.0001; r =Δ0.51,p <0.0001)和updrs-v分数(r = 0.46,p <0.0001; r =Δ0.45,p <0.0001)。 MIR-132-3P和MIR-146A-5P的曲线(AUC)结果下的区域鉴别来自健康对照的PD患者为0.7325(95%CI = 0.6400-0.8251)和0.7295(95%CI = 0.3658-0.8232 )。此外,关于来自正常Pd患者的判断严重PD患者的miR-132-3p和miR-146-5p的AUC结果为0.8175(95%CI = 0.729-0.9121)和0.7921(95%CI = 0.6937-0.8905)。换句话说,miR-132-3p和miR-146a-5p都可以作为有希望的生物标志物,用于早期诊断PD。

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