| Literature DB >> 32322100 |
Nicholas J Ashton1,2,3,4, Abdul Hye3,4, Anto P Rajkumar3,4,5, Antoine Leuzy6, Stuart Snowden7, Marc Suárez-Calvet1,8,9, Thomas K Karikari1, Michael Schöll1,2,6,10, Renaud La Joie11, Gil D Rabinovici11, Kina Höglund1,12, Clive Ballard13, Tibor Hortobágyi3,14, Per Svenningsson3,15, Kaj Blennow1,16, Henrik Zetterberg1,16,17,18, Dag Aarsland19,20,21.
Abstract
Cerebrospinal fluid analyses and neuroimaging can identify the underlying pathophysiology at the earliest stage of some neurodegenerative disorders, but do not have the scalability needed for population screening. Therefore, a blood-based marker for such pathophysiology would have greater utility in a primary care setting and in eligibility screening for clinical trials. Rapid advances in ultra-sensitive assays have enabled the levels of pathological proteins to be measured in blood samples, but research has been predominantly focused on Alzheimer disease (AD). Nonetheless, proteins that were identified as potential blood-based biomarkers for AD, for example, amyloid-β, tau, phosphorylated tau and neurofilament light chain, are likely to be relevant to other neurodegenerative disorders that involve similar pathological processes and could also be useful for the differential diagnosis of clinical symptoms. This Review outlines the neuropathological, clinical, molecular imaging and cerebrospinal fluid features of the most common neurodegenerative disorders outside the AD continuum and gives an overview of the current status of blood-based biomarkers for these disorders.Entities:
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Year: 2020 PMID: 32322100 DOI: 10.1038/s41582-020-0348-0
Source DB: PubMed Journal: Nat Rev Neurol ISSN: 1759-4758 Impact factor: 42.937