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Grants > Assessing the Impact of Blood Brain Barrier Dysfunction on CSF Tau Levels in Alzheimer’s Disease Updated On: Jan. 20, 2025
Alzheimer's Disease Research Grant

Assessing the Impact of Blood Brain Barrier Dysfunction on CSF Tau Levels in Alzheimer’s Disease

Tau
a headshot of Dr. Gadhavi

Principal Investigator

Joshna Gadhavi, PhD

Emory University

Atlanta, GA, USA

About the Research Project

Program

Alzheimer's Disease Research

Award Type

Standard

Award Amount

$200,000

Active Dates

July 01, 2024 - June 30, 2026

Grant ID

A2024029F

Mentor(s)

Nicholas Seyfried, PhD, Emory University

Goals

The goal of the project is to identify novel biomarkers and key targets for BBB breakdown and explore how it may contribute to Alzheimer’s Disease diagnosis and progression.

Summary

Blood brain barrier (BBB) breakdown has been observed in various neurodegenerative diseases including Alzheimer’s disease. In a healthy brain, the BBB does not allow transportation of proteins or large molecules into the brain. However, due to BBB dysfunction, enhanced permeability of plasma derived proteins can be observed in different parts of brain regions, and has been proposed to lead to neurotoxicity, neuroinflammation, and oxidative stress. This project will identify novel biomarkers and key targets for BBB breakdown and explore how it may contributes to AD diagnosis and progression.

Unique and Innovative

1. Deep and comprehensive network driven proteomics by unbiased subtyping will help to resolve molecular heterogeneity across different patient demographics in the Alzheimer’s disease progression.
2. BBB damage has been reported due to aging. However, relation between various proteolytic enzymes such thrombin and MMPs and reduced tau level in CSF in association with BBB damage is yet to be understood. This study will provide novel insights about various proteolytic enzymatic cleavage sites for tau reduction and its role in BBB damage.

Foreseeable Benefits

This project will identify novel biomarkers for BBB breakdown and its association to Alzheimer’s disease diagnosis and progression.