A Comprehensive Study of Circulating Blood Linear RNA nominates CD55 and DLD as novel causal genes and early-stage biomarkers for Parkinson's Disease.

Aleksandra Beric, Sarp Sahin, Santiago Sanchez, Zining Yang, Ravindra Kumar, Isabel Alfradique-Dunham, Jessie Sanford, Daniel Western, Bridget Phillips, John P Budde, Richard J Perrin, Paul T Kotzbauer, Joel S Perlmutter, Scott A Norris, Carlos Cruchaga, Laura Ibanez
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Abstract

We leveraged transcriptomic data from 4,343 participants from four independent datasets to robustly identify and annotate circulating PD-associated transcripts. We identified 296 differentially expressed transcripts, 28 of which were transcribed from known PD-associated loci. Further, we found a significant overlap between our findings and transcripts dysregulated in brain, as well as proteins differentially accumulated in CSF. Expression of the identified transcripts was affected by genetic background including ancestry and PD-related mutations, and nearly half of the identified transcripts were dysregulated before symptom onset. The differentially expressed transcripts were utilized to develop three predictive models that distinguished between PD and healthy controls with a ROC AUC of 0.727-0.733. The predictive models were capable of detecting PD transcriptomic signatures even before symptom onset. One transcript, DLD, showed particular promise as an early stage, minimally invasive PD biomarker that was differentially expressed in whole blood, brain and CSF. This transcript significantly related to PD in the eQTL analyses and in two of the three predictive models.

一项循环血液线性RNA的综合研究表明CD55和DLD是帕金森病的新致病基因和早期生物标志物。
我们利用来自4个独立数据集的4343名参与者的转录组学数据来稳健地识别和注释循环pd相关转录本。我们鉴定了296个差异表达转录本,其中28个来自已知的pd相关位点。此外,我们发现我们的研究结果与大脑中转录物失调以及脑脊液中不同积累的蛋白质之间存在显著的重叠。鉴定的转录本的表达受遗传背景(包括祖先和pd相关突变)的影响,近一半鉴定的转录本在症状发作前失调。利用差异表达的转录本建立了三个预测模型,以区分PD和健康对照,ROC AUC为0.727-0.733。预测模型甚至能够在症状出现之前检测PD转录组特征。一种转录物,DLD,作为早期、微创PD生物标志物,在全血、脑和脑脊液中差异表达,显示出特别的前景。在eQTL分析和三个预测模型中的两个中,该转录本与PD显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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