Comparative methods for quantifying plasma biomarkers in Alzheimer's disease: Implications for the next frontier in cerebral amyloid angiopathy diagnostics

Author:

Muir Ryan T.123ORCID,Ismail Zahinoor234,Black Sandra E.56,Smith Eric E.123ORCID

Affiliation:

1. Calgary Stroke Program Department of Clinical Neurosciences University of Calgary Calgary Alberta Canada

2. Department of Community Health Sciences University of Calgary Calgary Alberta Canada

3. Hotchkiss Brain Institute University of Calgary Calgary Alberta Canada

4. Department of Psychiatry University of Calgary Calgary Alberta Canada

5. Division of Neurology Department of Medicine Sunnybrook Health Sciences Centre Toronto Ontario Canada

6. LC Campbell Cognitive Neurology Research Unit Dr Sandra Black Centre for Brain Resilience and Recovery, and Hurvitz Brain Sciences Program Sunnybrook Research Institute University of Toronto Toronto Ontario Canada

Abstract

AbstractPlasma amyloid beta (Aβ) and tau are emerging as accessible biomarkers for Alzheimer's disease (AD). However, many assays exist with variable test performances, highlighting the need for a comparative assessment to identify the most valid assays for future use in AD and to apply to other settings in which the same biomarkers may be useful, namely, cerebral amyloid angiopathy (CAA). CAA is a progressive cerebrovascular disease characterized by deposition of Aβ40 and Aβ42 in cortical and leptomeningeal vessels. Novel immunotherapies for AD can induce amyloid‐related imaging abnormalities resembling CAA‐related inflammation. Few studies have evaluated plasma biomarkers in CAA. Identifying a CAA signature could facilitate diagnosis, prognosis, and a safer selection of patients with AD for emerging immunotherapies. This review evaluates studies that compare the diagnostic test performance of plasma biomarker techniques in AD and cerebrovascular and plasma biomarker profiles of CAA; it also discusses novel hypotheses and future avenues for plasma biomarker research in CAA.

Funder

University of Calgary

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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