AI Article Synopsis

  • Cerebrospinal fluid analyses and neuroimaging help identify neurodegenerative disorder pathophysiology early, but aren't practical for widespread screening; a blood-based marker could be more effective for primary care and clinical trial eligibility.
  • Recent advancements in ultra-sensitive assays allow measurement of pathological proteins in blood, with a primary focus on Alzheimer disease (AD), but findings may also be relevant for other neurodegenerative disorders.
  • The Review discusses neuropathological and clinical features of common neurodegenerative disorders beyond AD and provides an overview of the current status of potential blood-based biomarkers for these conditions.

Article 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.

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Source
http://dx.doi.org/10.1038/s41582-020-0348-0DOI Listing

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