Literature DB >> 27228454

Glial biomarkers in human central nervous system disease.

Gwenn A Garden1, Brian M Campbell2.   

Abstract

There is a growing understanding that aberrant GLIA function is an underlying factor in psychiatric and neurological disorders. As drug discovery efforts begin to focus on glia-related targets, a key gap in knowledge includes the availability of validated biomarkers to help determine which patients suffer from dysfunction of glial cells or who may best respond by targeting glia-related drug mechanisms. Biomarkers are biological variables with a significant relationship to parameters of disease states and can be used as surrogate markers of disease pathology, progression, and/or responses to drug treatment. For example, imaging studies of the CNS enable localization and characterization of anatomical lesions without the need to isolate tissue for biopsy. Many biomarkers of disease pathology in the CNS involve assays of glial cell function and/or response to injury. Each major glia subtype (oligodendroglia, astroglia and microglia) are connected to a number of important and useful biomarkers. Here, we describe current and emerging glial based biomarker approaches for acute CNS injury and the major categories of chronic nervous system dysfunction including neurodegenerative, neuropsychiatric, neoplastic, and autoimmune disorders of the CNS. These descriptions are highlighted in the context of how biomarkers are employed to better understand the role of glia in human CNS disease and in the development of novel therapeutic treatments. GLIA 2016;64:1755-1771.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  cerebrospinal fluid; inflammation; magnetic resonance imaging; neuroimaging; positron emission tomography

Mesh:

Substances:

Year:  2016        PMID: 27228454      PMCID: PMC5575821          DOI: 10.1002/glia.22998

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


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