Blood transcriptomic signatures associated with molecular changes in the brain and clinical outcomes in Parkinson’s disease

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作者
Krithi Irmady
Caryn R. Hale
Rizwana Qadri
John Fak
Sitsandziwe Simelane
Thomas Carroll
Serge Przedborski
Robert B. Darnell
机构
[1] The Rockefeller University,Laboratory of Molecular Neuro
[2] The Rockefeller University,oncology
[3] Columbia University,Bioinformatics Resource Center
[4] Columbia University,Department of Neurology
[5] Columbia University,Department of Pathology & Cell Biology
[6] The Rockefeller University,Department of Neuroscience
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The ability to use blood to predict the outcomes of Parkinson’s disease, including disease progression and cognitive and motor complications, would be of significant clinical value. We undertook bulk RNA sequencing from the caudate and putamen of postmortem Parkinson’s disease (n = 35) and control (n = 40) striatum, and compared molecular profiles with clinical features and bulk RNA sequencing data obtained from antemortem peripheral blood. Cognitive and motor complications of Parkinson’s disease were associated with molecular changes in the caudate (stress response) and putamen (endothelial pathways) respectively. Later and earlier-onset Parkinson’s disease were molecularly distinct, and disease duration was associated with changes in caudate (oligodendrocyte development) and putamen (cellular senescence), respectively. Transcriptome patterns in the postmortem Parkinson’s disease brain were also evident in antemortem peripheral blood, and correlated with clinical features of the disease. Together, these findings identify molecular signatures in Parkinson’s disease patients’ brain and blood of potential pathophysiologic and prognostic importance.
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