# Salivary total tau: a clinically practical measure of tau neuropathology in Alzheimer’s disease

**Authors:** Alison R. Bamford, Christopher Logan, Quynh Theresa Do, Kelly Nguyen, Liv C. McMillan, Michael A. Yassa, William R. Shankle, Elizabeth A. Thomas

PMC · DOI: 10.1007/s00415-026-13651-1 · Journal of Neurology · 2026-02-18

## TL;DR

This study shows that measuring total tau in saliva could be a non-invasive way to detect Alzheimer's disease pathology.

## Contribution

The study introduces salivary total tau as a potential non-invasive biomarker for Alzheimer's disease.

## Key findings

- Salivary total tau levels were significantly higher in Alzheimer's and mild Alzheimer's patients compared to cognitively unimpaired individuals.
- Salivary total tau correlated with cerebrospinal fluid biomarkers of Alzheimer's disease.
- Salivary total tau predicted Alzheimer's cases with an area under the curve of 0.834.

## Abstract

Neurofibrillary tangles, consisting of intracellular accumulations of the protein tau, are a hallmark feature of Alzheimer’s disease (AD), and are thought to contribute to neuronal dysfunction and death during the disease process. The quantification of tau proteins in cerebrospinal fluid (CSF) or plasma has enormous utility for AD diagnosis; however, validated non-invasive measures of tau protein are lacking and would have added value for widespread screening. In this study, we quantified the levels of total tau (t-tau), along with neurofilament light (NfL) and glial fibrillary acidic protein (GFAP), in saliva samples from 111 participants, including those with CSF biomarker-confirmed AD, mild AD, non-AD cognitively impaired (CI) and cognitively unimpaired (CU) older adults, using immunoassays on the Meso Scale Discovery platform. We find that salivary levels of t-tau were significantly elevated in AD and mild AD, but not other CI patients, compared to CU adults, while salivary levels of NfL and GFAP showed no significant differences across cohorts. In addition, we found that salivary t-tau was significantly correlated with CSF biomarker measures, including significant positive correlations with CSF t-tau and p-tau 181 (0.257; p = 0.016 and 0.276; p = 0.009 for t-tau and p-tau 181, respectively). Salivary t-tau was also found to predict AD cases compared to CU individuals with an area under the curve of 0.834 (95% CI 0.74–0.93; p < 0.0001). Finally, we observed that salivary t-tau levels were significantly negatively correlated with cognitive performance in AD patients, as well as all individuals together. These findings suggest that salivary t-tau might represent a non-invasive biomarker specific to AD pathology and could aid in early detection of AD or for clinical screening purposes.

The online version contains supplementary material available at 10.1007/s00415-026-13651-1.

## Linked entities

- **Proteins:** MAPT (microtubule associated protein tau), NEFL (neurofilament light chain), GFAP (glial fibrillary acidic protein)
- **Diseases:** Alzheimer’s disease (MONDO:0004975), AD (MONDO:0004975)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, RMDN1 (regulator of microtubule dynamics 1) [NCBI Gene 51115] {aka CGI-90, FAM82B, RMD-1, RMD1}
- **Diseases:** neurodegeneration (MESH:D019636), neuronal dysfunction and death (MESH:D003643), AD (MESH:D000544), impaired (MESH:D060825), Huntington's disease (MESH:D006816), cerebral ischemia (MESH:D002545), cerebrovascular disease (MESH:D002561), tauopathies (MESH:D024801), neuronal loss (MESH:D009410), cerebral amyloid angiopathy (MESH:D016657), frontal temporal lobe dementia (MESH:C538521), multisystem atrophy (MESH:D019578), dementia (MESH:D003704), amyloid (MESH:C000718787), tau tangles (MESH:C536599), AD cognitively impaired (MESH:D003072), lacunar infarcts (MESH:D059409), Neurofibrillary tangles (MESH:D055956), memory impairment (MESH:D008569)
- **Chemicals:** 1X (-), EDTA (MESH:D004492)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12917055