AI Article Synopsis

  • The study compares plasma amyloid beta (Aβ42) and tau levels in Alzheimer's disease (AD) patients from two different hospitals in the U.S. and Taiwan using ultra-sensitive IMR assays.
  • Significant increases in tau levels were found in AD patients from both cohorts, while Aβ42 levels only increased in the Taiwan group.
  • The research determined that tau levels could identify probable AD with high accuracy, and combining Aβ42 and tau data further improved diagnostic accuracy, suggesting these measures can help in diagnosing AD clinically.

Article Abstract

The utility of plasma amyloid beta (Aβ) and tau levels for the clinical diagnosis of Alzheimer's disease (AD) dementia has been controversial. The main objective of this study was to compare Aβ42 and tau levels measured by the ultra-sensitive immunomagnetic reduction (IMR) assays in plasma samples collected at the Banner Sun Health Institute (BSHRI) (United States) with those from the National Taiwan University Hospital (NTUH) (Taiwan). Significant increase in tau levels were detected in AD subjects from both cohorts, while Aβ42 levels were increased only in the NTUH cohort. A regression model incorporating age showed that tau levels identified probable ADs with 81 and 96% accuracy in the BSHRI and NTUH cohorts, respectively, while computed products of Aβ42 and tau increased the accuracy to 84% in the BSHRI cohorts. Using 382.68 (pg/ml) as the cut-off value, the product achieved 92% accuracy in identifying AD in the combined cohorts. Overall findings support that plasma Aβ42 and tau assayed by IMR technology can be used to assist in the clinical diagnosis of AD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522888PMC
http://dx.doi.org/10.3389/fnagi.2017.00226DOI Listing

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