| Literature DB >> 26220939 |
Joseph J Locascio1, Shirley Eberly2, Zhixiang Liao3, Ganqiang Liu3, Ashley N Hoesing4, Karen Duong4, Ana Trisini-Lipsanopoulos4, Kaltra Dhima4, Albert Y Hung5, Alice W Flaherty6, Michael A Schwarzschild5, Michael T Hayes7, Anne-Marie Wills8, U Shivraj Sohur5, Nicte I Mejia5, Dennis J Selkoe9, David Oakes2, Ira Shoulson10, Xianjun Dong3, Ken Marek10, Bin Zheng3, Adrian Ivinson11, Bradley T Hyman8, John H Growdon5, Lewis R Sudarsky7, Michael G Schlossmacher12, Bernard Ravina13, Clemens R Scherzer14.
Abstract
There are no cures for neurodegenerative diseases and this is partially due to the difficulty of monitoring pathogenic molecules in patients during life. The Parkinson's disease gene α-synuclein (SNCA) is selectively expressed in blood cells and neurons. Here we show that SNCA transcripts in circulating blood cells are paradoxically reduced in early stage, untreated and dopamine transporter neuroimaging-supported Parkinson's disease in three independent regional, national, and international populations representing 500 cases and 363 controls and on three analogue and digital platforms with P < 0.0001 in meta-analysis. Individuals with SNCA transcripts in the lowest quartile of counts had an odds ratio for Parkinson's disease of 2.45 compared to individuals in the highest quartile. Disease-relevant transcript isoforms were low even near disease onset. Importantly, low SNCA transcript abundance predicted cognitive decline in patients with Parkinson's disease during up to 5 years of longitudinal follow-up. This study reveals a consistent association of reduced SNCA transcripts in accessible peripheral blood and early-stage Parkinson's disease in 863 participants and suggests a clinical role as potential predictor of cognitive decline. Moreover, the three independent biobank cohorts provide a generally useful platform for rapidly validating any biological marker of this common disease.Entities:
Keywords: biobank; biomarker; cognitive decline; gene expression; mitochondria; α-synuclein
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Year: 2015 PMID: 26220939 PMCID: PMC4643625 DOI: 10.1093/brain/awv202
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501