Abstract
There is a need for an accessible biomarker that can complement
current cerebrospinal fluid (CSF) and imaging biomarkers in an accurate
and early diagnosis of Alzheimer disease (AD). Saliva is a rich source of
potential biomarkers and proteins related to neurodegenerative disorders
have been shown to be present in this matrix, including tau. In this
study, we quantified salivary total tau (t-tau) concentration in 160
healthy elderly control (HEC), 60 mild cognitive impairment (MCI) and 54
Alzheimer's disease (AD) participants using ultra-sensitive Single
molecule array (Simoa) technology. No median difference in salivary t-tau
concentration was found between AD and MCI or HEC (12.3 ng/L, 9.8 ng/L
and 9.6 ng/L, respectively, P = 0.219). In addition, there was no
association of salivary t-tau concentration with neurophysiological
assessment or structural MRI. Despite a nominal increase in AD, due to
the large overlaps in concentrations between clinical groups, we conclude
that salivary t-tau is neither a suitable biomarker for AD nor for
cognitive impairment.
current cerebrospinal fluid (CSF) and imaging biomarkers in an accurate
and early diagnosis of Alzheimer disease (AD). Saliva is a rich source of
potential biomarkers and proteins related to neurodegenerative disorders
have been shown to be present in this matrix, including tau. In this
study, we quantified salivary total tau (t-tau) concentration in 160
healthy elderly control (HEC), 60 mild cognitive impairment (MCI) and 54
Alzheimer's disease (AD) participants using ultra-sensitive Single
molecule array (Simoa) technology. No median difference in salivary t-tau
concentration was found between AD and MCI or HEC (12.3 ng/L, 9.8 ng/L
and 9.6 ng/L, respectively, P = 0.219). In addition, there was no
association of salivary t-tau concentration with neurophysiological
assessment or structural MRI. Despite a nominal increase in AD, due to
the large overlaps in concentrations between clinical groups, we conclude
that salivary t-tau is neither a suitable biomarker for AD nor for
cognitive impairment.
Original language | English |
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Pages (from-to) | 125-127 |
Number of pages | 3 |
Journal | Neurobiology of Aging |
Volume | 70 |
Early online date | 20 Jun 2018 |
DOIs | |
Publication status | Published - Oct 2018 |