Abstract

Alzheimer’s disease (AD) and the associated neurodegenerative dementia have become of increasing concern in healthcare. The tau protein has been considered a key hallmark of progressive neurodegeneration. In this paper, a large-scale analysis of five datasets (more than 2500 people) from the Global Alzheimer’s Association Interactive Network (GAAIN) databases was performed to investigate the association between the level of tau protein, including total tau and phosphorylated tau (p-tau), in cerebrospinal fluid (CSF) and cognitive status. Statistically significant (or marginally significant) high total tau or p-tau concentrations in CSF were observed in dementia patients compared with healthy people in all datasets. There is also a statistically significant (or marginally significant) negative correlation between p-tau concentrations in CSF and Folstein Mini-Mental State Examination (MMSE) scores. In addition, transcriptomic data derived from mouse microglial cells showed multiple genes upregulated in Toll-like receptor signaling and Alzheimer’s disease pathways, including TNF, TLR2, IL-1β, and COX subunits, suggesting that the mechanism of action that relates p-tau and MMSE scores may be through overactivation of pro-inflammatory microglial activity by Aβ peptides, TNF-mediated hyperphosphorylation of tau, and the infectious spread of pathological tau across healthy neurons. Our results not only confirmed the association between tau protein level and cognitive status in a large population but also provided useful information for the understanding of the role of tau in neurodegeneration and the development of dementia.

Highlights

  • Alzheimer’s disease (AD) is a neurodegenerative condition diagnosed by decline in cognitive faculties and memory

  • A statistically significant difference in gender distribution was observed between the healthy group (n = 492 females) and the group with dementia (n = 73 females; p = 0.01)

  • Statistically significant (p < 0.001) difference in age was observed in which the average age for the healthy group was 72.94 and the average age for the dementia group was 75.31

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Summary

Introduction

Alzheimer’s disease (AD) is a neurodegenerative condition diagnosed by decline in cognitive faculties and memory. It has become one of the most common forms of cognitive impairment and is characterized by neuronal destruction [1]. With the psychological and economic toll that late-stage AD pathology can create, greater pressure is placed on early diagnosis in order to initiate early treatment. Phosphorylated tau (p-tau) has been considered to be related to progressive neurodegeneration. Tau is a highly soluble microtubule-associated protein that aids in the stabilization and integrity of healthy neurons [2]. Tau is encoded by a single gene (MAPT) located on chromosome 17 that contains

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