Concepedia

Publication | Open Access

Plasma tau in Alzheimer disease

503

Citations

19

References

2016

Year

TLDR

The study aimed to determine whether plasma tau levels differ in Alzheimer disease and relate to cognition, CSF biomarkers, brain atrophy, and metabolism, using data from the ADNI and BioFINDER cohorts. Researchers measured plasma tau in 1,284 participants from ADNI and BioFINDER and examined its associations with diagnosis, CSF biomarkers, MRI, PET, and cognition. Plasma tau was weakly associated with AD diagnosis and CSF biomarkers, correlated with cognitive decline, atrophy, and hypometabolism longitudinally, but its overlap with normal aging limits its use as an individual biomarker.

Abstract

To test whether plasma tau is altered in Alzheimer disease (AD) and whether it is related to changes in cognition, CSF biomarkers of AD pathology (including β-amyloid [Aβ] and tau), brain atrophy, and brain metabolism.This was a study of plasma tau in prospectively followed patients with AD (n = 179), patients with mild cognitive impairment (n = 195), and cognitive healthy controls (n = 189) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and cross-sectionally studied patients with AD (n = 61), mild cognitive impairment (n = 212), and subjective cognitive decline (n = 174) and controls (n = 274) from the Biomarkers for Identifying Neurodegenerative Disorders Early and Reliably (BioFINDER) study at Lund University, Sweden. A total of 1284 participants were studied. Associations were tested between plasma tau and diagnosis, CSF biomarkers, MRI measures, 18fluorodeoxyglucose-PET, and cognition.Higher plasma tau was associated with AD dementia, higher CSF tau, and lower CSF Aβ42, but the correlations were weak and differed between ADNI and BioFINDER. Longitudinal analysis in ADNI showed significant associations between plasma tau and worse cognition, more atrophy, and more hypometabolism during follow-up.Plasma tau partly reflects AD pathology, but the overlap between normal aging and AD is large, especially in patients without dementia. Despite group-level differences, these results do not support plasma tau as an AD biomarker in individual people. Future studies may test longitudinal plasma tau measurements in AD.

References

YearCitations

Page 1