Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jul 26;11(7):e0159099.
doi: 10.1371/journal.pone.0159099. eCollection 2016.

Estimation of Tau and Phosphorylated Tau181 in Serum of Alzheimer's Disease and Mild Cognitive Impairment Patients

Affiliations

Estimation of Tau and Phosphorylated Tau181 in Serum of Alzheimer's Disease and Mild Cognitive Impairment Patients

Shashank Shekhar et al. PLoS One. .

Abstract

The elevated level of cerebrospinal fluid (CSF) Tau and phosphorylated Tau181 (p-Tau181) proteins are well established hallmarks of Alzheimer's disease (AD). Elevated level of p-Tau181 can differentiate AD from other neurodegenerative disease. However, the expression level of these proteins in serum of AD patient is not well set up. This study sought to evaluate the level of Tau and p-Tau181 in serum of AD, and mild cognitive impairment (MCI) patients for an alternative approach to establish protein-based markers by convenient way. Blood samples were collected from 39 AD patients, 37 MCI patients and 37 elderly individuals as controls. The levels of Tau and p-Tau181 in the serum of the different groups were measured by label free real time Surface Plasmon Resonance technology by using specific antibodies, and were further confirmed by the conventional western blot method. An appropriate statistical analysis, including Receiver Operating Characteristic (ROC), was performed. The concentrations of serum Tau and p-Tau181 were significantly higher (p<0.00001) in AD (Tau; 47.49±9.00ng/μL, p-Tau181; 0.161±0.04 ng/μL) compared to MCI (Tau; 39.26±7.78 ng/μL, p-Tau181; 0.135±0.02 ng/μL) and were further higher compared to elderly controls (Tau; 34.92±6.58 ng/μL, p-Tau181; 0.122±0.01 ng/ μL). A significant (p<0.0001) downhill correlation was found between Tau as well as p-Tau181 levels with HMSE and MoCA score. This study for the first time reports the concentration of Tau and p-Tau181 in serum of AD and MCI patients. The cutoff values of Tau and p-Tau181 of AD and MCI patients with sensitivity and specificity reveal that serum level of these proteins can be used as a predictive marker for AD and MCI.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Scatter graph showing the serum level of Tau (A) and p-Tau181 (B) in AD, MCI and elderly control.
Fig 2
Fig 2. ROC analysis showing area under curve, threshold value with sensitivity and specificity, for Tau: (A) AD vs control (B) MCI vs control for p-Tau181: (C) AD vs control (D) MCI vs control.

References

    1. World Health Organization. Dementia: a Public Health Priority (World Health Organization, Geneva, 2012).
    1. Shaji KS, Jotheeswaran AT, Girish N, Srikala B, Amit D, Meera P, et al. (2010) Alzheimer’s & Related Disorders Society of India. The Dementia India Report: prevalence, impact, costs and services for Dementia: Executive Summary. ARDSI, New Delhi.
    1. Mark M, Amrita KC, Massimo SF, Xiaogang Z, Timothy RM, Linda HM, et al. (2014) Plasma phospholipids identify antecedent memory impairment in older adults. Nature medicine. 20: 415–418. 10.1038/nm.3466 - DOI - PMC - PubMed
    1. Blennow K, Hampel H, Weiner M, Zetterberg H. (2010)Cerebrospinal fluid and plasma biomarkers in Alzheimer disease. Nat. Rev. Neurol 6: 131–144. 10.1038/nrneurol.2010.4 - DOI - PubMed
    1. Billingsley ML, Kincaid RL. (1997) "Regulated phosphorylation and dephosphorylation of tau protein: effects on microtubule interaction, intracellular trafficking and neurodegeneration". Biochem. J. 323: 577–91. - PMC - PubMed

LinkOut - more resources