血浆细胞转录组包含帕金森病特征,可为临床诊断提供依据。

Aleksandra Beric, Alejandro Cisterna-García, Charissa Martin, Ravindra Kumar, Isabel Alfradique-Dunham, Kevin Boyer, Ibrahim Olabayode Saliu, Shinnosuke Yamada, Jessie Sanford, Daniel Western, Menghan Liu, Ignacio Alvarez, Joel S Perlmutter, Scott A Norris, Pau Pastor, Guoyan Zhao, Juan Botia, Laura Ibanez
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引用次数: 0

摘要

我们的目标是找出与帕金森病(PD)相关的无血浆细胞转录本(cfRNA),这些转录本在区分帕金森病与健康对照组方面也具有很高的预测价值。利用来自两个不同运动障碍中心的两个独立人群,我们经过荟萃分析确定了 2188 个差异表达的 cfRNA。鉴定出的转录本富集在与帕金森病相关的通路中,如帕金森病通路(p=9.26×10 -4)、泛素介导的蛋白水解通路(p=7.41×10 -5)和内吞通路(p=4.21×10 -6)。利用内部和公开的大脑、全血和无细胞血浆转录组和蛋白质组 PD 数据集,我们发现不同组织和不同生物层中调控失调的生物物种之间存在显著重叠。我们建立了三个预测模型,其中包含的转录本数量不断增加,这些模型能将脊髓灰质炎与健康对照区分开来,其 ROC 曲线下面积 (AUC) ≥0.85。最后,我们发现其中几个预测转录本与 UPDRS-III 测定的症状严重程度显著相关。总之,我们证明了 cfRNA 含有病理特征,有可能被用作生物标记物来帮助诊断和监测帕金森病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma acellular transcriptome contains Parkinson's disease signatures that can inform clinical diagnosis.

We aimed to identify plasma cell-free transcripts (cfRNA) associated with Parkinson's disease (PD) that also have a high predictive value to differentiate PD from healthy controls. Leveraging two independent populations from two different movement disorder centers we identified 2,188 differentially expressed cfRNAs after meta-analysis. The identified transcripts were enriched in PD relevant pathways, such as PD (p=9.26×10-4), ubiquitin-mediated proteolysis (p=7.41×10-5) and endocytosis (p=4.21×10-6). Utilizing in-house and publicly available brain, whole blood, and acellular plasma transcriptomic and proteomic PD datasets, we found significant overlap across dysregulated biological species in the different tissues and the different biological layers. We developed three predictive models containing increasing number of transcripts that can distinguish PD from healthy control with an area under the ROC Curve (AUC) ≥0.85. Finally, we showed that several of the predictive transcripts significantly correlate with symptom severity measured by UPDRS-III. Overall, we have demonstrated that cfRNA contains pathological signatures and has the potential to be utilized as biomarker to aid in PD diagnostics and monitoring.

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