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
{"title":"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。","authors":"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","doi":"10.1101/2024.10.18.24315717","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>-4</sup>), ubiquitin-mediated proteolysis (p=7.41×10<sup>-5</sup>) and endocytosis (p=4.21×10<sup>-6</sup>). 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.</p>","PeriodicalId":94281,"journal":{"name":"medRxiv : the preprint server for health sciences","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11527085/pdf/","citationCount":"0","resultStr":"{\"title\":\"Plasma acellular transcriptome contains Parkinson's disease signatures that can inform clinical diagnosis.\",\"authors\":\"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\",\"doi\":\"10.1101/2024.10.18.24315717\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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<sup>-4</sup>), ubiquitin-mediated proteolysis (p=7.41×10<sup>-5</sup>) and endocytosis (p=4.21×10<sup>-6</sup>). 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.</p>\",\"PeriodicalId\":94281,\"journal\":{\"name\":\"medRxiv : the preprint server for health sciences\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11527085/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"medRxiv : the preprint server for health sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.10.18.24315717\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv : the preprint server for health sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.10.18.24315717","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.