Cheng Yan, Zhai Hongjiang, Liu Yong, Yang Yunzhou, Fang Bo, Song Mingxiang, Zhong Ping
Department of Neurology, Suzhou Hospital of Anhui Medical University, Suzhou, Anhui, People's Republic of China.
Department of Neurology, Lu'an Hospital of Anhui Medical University, Lu'an, Anhui, People's Republic of China.
Neuropsychiatr Dis Treat. 2025 Feb 28;21:437-449. doi: 10.2147/NDT.S511671. eCollection 2025.
Parkinson's disease (PD) is a common neurodegenerative disorder. Iron metabolism abnormalities have been reported in PD patients and may contribute to disease pathogenesis. Our study aimed to explore key genes associated with iron metabolism in PD patients.
Three datasets and iron metabolism-related genes (IMRGs) were collected from the public database, and the datasets were merged into a combined dataset. PD-related differentially expressed genes (DEGs) were obtained and intersected with IMRGs to acquire iron metabolism-related DEGs (IMRDEGs). Subsequently, the IMRDEGs were subjected to functional enrichment and ROC analyses. Finally, key genes were identified, followed by the construction and evaluation of a risk score model, drug prediction, and RT-qPCR analysis.
A total of 24 IMRDEGs were obtained. The AUC values of the 24 IMRDEGs ranged from 0.599 to 0.781. After logistic regression and the SVM analyses, a total of 10 key genes were identified, followed by the construction of the risk score model. The AUC value of the risk score model was 0.953, demonstrating good diagnostic value. The calibration curve and decision curve analysis showed that the risk score model has good predictive performance and clinical benefit for PD patients. Additionally, a total of 49 drugs were predicted.
A total of 10 key genes were identified as potential biomarkers, and the risk score model was constructed for PD patients, exhibiting good diagnostic. This study may provide potential biomarkers for PD patients, promoting an understanding of the pathogenesis of PD.
帕金森病(PD)是一种常见的神经退行性疾病。已有报道称PD患者存在铁代谢异常,这可能与疾病的发病机制有关。我们的研究旨在探索PD患者中与铁代谢相关的关键基因。
从公共数据库收集三个数据集和铁代谢相关基因(IMRGs),并将这些数据集合并为一个组合数据集。获取与PD相关的差异表达基因(DEGs),并与IMRGs进行交集分析,以获得与铁代谢相关的DEGs(IMRDEGs)。随后,对IMRDEGs进行功能富集和ROC分析。最后,鉴定关键基因,接着构建并评估风险评分模型、进行药物预测和RT-qPCR分析。
共获得24个IMRDEGs。这24个IMRDEGs的AUC值范围为0.599至0.781。经过逻辑回归和支持向量机分析后,共鉴定出10个关键基因,随后构建了风险评分模型。风险评分模型的AUC值为0.953,显示出良好的诊断价值。校准曲线和决策曲线分析表明,风险评分模型对PD患者具有良好的预测性能和临床益处。此外,共预测出49种药物。
共鉴定出10个关键基因作为潜在生物标志物,并为PD患者构建了风险评分模型,显示出良好的诊断性能。本研究可能为PD患者提供潜在生物标志物,促进对PD发病机制的理解。