Plasma Aβ42 and Total Tau Predict Cognitive Decline in Amnestic Mild Cognitive Impairment

Ting-Bin Chen1,2,3,4, Yi-Jung Lee1,5, Szu-Ying Lin6

  • 1Institute of Brain Science, National Yang-Ming University, Taipei, Taiwan.

Scientific Reports
|September 29, 2019
PubMed

Insights

High levels of plasma amyloid-beta 42 (Aβ42) and total-tau (t-tau) predict cognitive decline in individuals with mild cognitive impairment (MCI). Combining these biomarkers offers enhanced predictive value for future memory loss.

Area of Science:

  • Neurology
  • Biochemistry
  • Gerontology

Background:

  • Alzheimer disease (AD) is linked to brain amyloid-beta (Aβ) and tau peptide levels.
  • Mild cognitive impairment (MCI) is a prodromal stage of AD, characterized by cognitive decline.
  • Identifying reliable biomarkers for MCI progression is crucial for early intervention.

Purpose of the Study:

  • To investigate the predictive ability of plasma Aβ42 and total-tau (t-tau) for cognitive decline in amnestic MCI.
  • To evaluate the diagnostic performance of these plasma biomarkers individually and in combination.

Main Methods:

  • Quantification of plasma Aβ42 and t-tau using immunomagnetic reduction (IMR) assay in 22 amnestic MCI participants.
  • Neuropsychological testing at baseline and annual follow-up (average 1.5 years) to assess cognitive performance.
  • Statistical analysis to determine the predictive value of plasma biomarkers for cognitive status changes.

Main Results:

  • Elevated plasma Aβ42 and t-tau levels correlated with poorer episodic verbal memory at baseline.
  • Higher plasma Aβ42 and t-tau were associated with cognitive decline during the follow-up period.
  • The combined product of plasma Aβ42 and t-tau demonstrated superior discriminatory value for predicting cognitive decline compared to individual markers.

Conclusions:

  • Plasma Aβ42 and t-tau show potential as predictive biomarkers for cognitive decline in amnestic MCI.
  • The combination of plasma Aβ42 and t-tau may enhance the identification of individuals at risk for future cognitive deterioration.
  • Further large-scale, long-term studies are necessary to validate these preliminary findings and establish their clinical utility.

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