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- W2736708071 abstract "The utility of the levels of amyloid beta (Aβ) peptide and tau in blood for diagnosis, drug development, and assessment of clinical trials for Alzheimer's disease (AD) has not been established. The lack of availability of ultra-sensitive assays is one critical issue that has impeded progress. The levels of Aβ species and tau in plasma and serum are much lower than levels in cerebrospinal fluid. Furthermore, plasma or serum contain high levels of assay-interfering factors, resulting in difficulties in the commonly used singulex or multiplex ELISA platforms. In this review, we focus on two modern immune-complex-based technologies that show promise to advance this field. These innovative technologies are immunomagnetic reduction technology and single molecule array technology. We describe the technologies and discuss the published studies using these technologies. Currently, the potential of utilizing these technologies to advance Aβ and tau as blood-based biomarkers for AD requires further validation using already collected large sets of samples, as well as new cohorts and population-based longitudinal studies." @default.
- W2736708071 created "2017-07-31" @default.
- W2736708071 creator A5022856463 @default.
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- W2736708071 creator A5059245617 @default.
- W2736708071 date "2017-07-01" @default.
- W2736708071 modified "2023-10-18" @default.
- W2736708071 title "Amyloid Beta and Tau as Alzheimer’s Disease Blood Biomarkers: Promise From New Technologies" @default.
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- W2736708071 doi "https://doi.org/10.1007/s40120-017-0074-8" @default.
- W2736708071 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5520820" @default.
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- W2736708071 hasPublicationYear "2017" @default.
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