GFAP as a Potential Biomarker for Alzheimer’s Disease: A Systematic Review and Meta-Analysis

Author:

Kim Ka Young12ORCID,Shin Ki Young3,Chang Keun-A245ORCID

Affiliation:

1. Department of Nursing, College of Nursing, Gachon University, Incheon 21936, Republic of Korea

2. Neuroscience Research Institute, Gachon University, Incheon 21565, Republic of Korea

3. Bio-MAX Institute, Seoul National University, Seoul 08826, Republic of Korea

4. Department of Pharmacology, College of Medicine, Gachon University, Incheon 21936, Republic of Korea

5. Bio-Medical Sciences, Gachon Advanced Institute for Health Sciences and Technology, Gachon University, Incheon 21936, Republic of Korea

Abstract

Blood biomarkers have been considered tools for the diagnosis, prognosis, and monitoring of Alzheimer’s disease (AD). Although amyloid-β peptide (Aβ) and tau are primarily blood biomarkers, recent studies have identified other reliable candidates that can serve as measurable indicators of pathological conditions. One such candidate is the glial fibrillary acidic protein (GFAP), an astrocytic cytoskeletal protein that can be detected in blood samples. Increasing evidence suggests that blood GFAP levels can be used to detect early-stage AD. In this systematic review and meta-analysis, we aimed to evaluate GFAP in peripheral blood as a biomarker for AD and provide an overview of the evidence regarding its utility. Our analysis revealed that the GFAP level in the blood was higher in the Aβ-positive group than in the negative groups, and in individuals with AD or mild cognitive impairment (MCI) compared to the healthy controls. Therefore, we believe that the clinical use of blood GFAP measurements has the potential to accelerate the diagnosis and improve the prognosis of AD.

Funder

National Research Foundation of Korea

Basic Science Research Program through the NRF of Korea

Publisher

MDPI AG

Subject

General Medicine

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