4.6 Review

Microglia Biomarkers in Alzheimer's Disease

Journal

MOLECULAR NEUROBIOLOGY
Volume 58, Issue 7, Pages 3388-3404

Publisher

SPRINGER
DOI: 10.1007/s12035-021-02348-3

Keywords

Alzheimer’ s disease; Microglia; Biomarkers; Fluid; Imaging

Categories

Funding

  1. Shanghai Municipal Science and Technology Major Project [2018SHZDZX01]
  2. ZJLab
  3. Shanghai Center for Brain Science and Brain-Inspired Technology
  4. Tianqiao and Chrissy Chen Institute
  5. State Key Laboratory of Neurobiology and Frontiers Center for Brain Science of Ministry of Education, Fudan University

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Early detection and clinical diagnosis of Alzheimer's disease are crucial. Microglia, considered to be a potential factor in the pathological mechanisms, are being studied for specific and sensitive biomarkers to address the challenges of AD.
Early detection and clinical diagnosis of Alzheimer's disease (AD) have become an extremely important link in the prevention and treatment of AD. Because of the occult onset, the diagnosis and treatment of AD based on clinical symptoms are increasingly challenged by current severe situations. Therefore, molecular diagnosis models based on early AD pathological markers have received more attention. Among the possible pathological mechanisms, microglia which are necessary for normal brain function are highly expected and have been continuously studied in various models. Several AD biomarkers already exist, but currently there is a paucity of specific and sensitive microglia biomarkers which can accurately measure preclinical AD. Bringing microglia biomarkers into the molecular diagnostic system which is based on fluid and neuroimaging will play an important role in future scientific research and clinical practice. Furthermore, developing novel, more specific, and sensitive microglia biomarkers will make it possible to pharmaceutically target chemical pathways that preserve beneficial microglial functions in response to AD pathology. This review discusses microglia biomarkers in the context of AD.

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