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Review
. 2020 May;16(5):265-284.
doi: 10.1038/s41582-020-0348-0. Epub 2020 Apr 22.

An update on blood-based biomarkers for non-Alzheimer neurodegenerative disorders

Affiliations
Review

An update on blood-based biomarkers for non-Alzheimer neurodegenerative disorders

Nicholas J Ashton et al. Nat Rev Neurol. 2020 May.

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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References

    1. Cummings, J. Lessons learned from Alzheimer disease: clinical trials with negative outcomes. Clin. Transl Sci. 11, 147–152 (2018). - DOI
    1. Kovacs, G. G. Molecular pathological classification of neurodegenerative diseases: turning towards precision medicine. Int. J. Mol. Sci. 17, 189 (2016). - PMC - DOI - PubMed
    1. Neary, D. et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 51, 1546–1554 (1998). Consensus criteria for the clinical diagnosis of the three syndromes associated with frontotemporal lobar degeneration: frontotemporal dementia, progressive nonfluent aphasia and semantic dementia. - DOI
    1. McKeith, I. G. et al. Diagnosis and management of dementia with Lewy bodies: fourth consensus report of the DLB consortium. Neurology 89, 88–100 (2017). Consensus criteria for the clinical diagnosis of dementia with Lewy bodies and recommendations on the clinical management of the disease. - PMC - DOI - PubMed
    1. Hoglinger, G. U. et al. Clinical diagnosis of progressive supranuclear palsy: the Movement Disorder Society criteria. Mov. Disord. 32, 853–864 (2017). Clinical diagnostic criteria for progressive supranuclear palsy. - PMC - DOI - PubMed

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