4.7 Review

Serum glial fibrillary acidic protein is a body fluid biomarker: A valuable prognostic for neurological disease - A systematic review

期刊

INTERNATIONAL IMMUNOPHARMACOLOGY
卷 107, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.intimp.2022.108624

关键词

Blood; COVID-19; GFAP; Intermediate filament; Neurodegeneration

资金

  1. FAPESE
  2. FAPITEC-SE
  3. CNPq
  4. CAPES

向作者/读者索取更多资源

Astrocytes, as the most abundant cell type in the human central nervous system, play a crucial role in the regulation of neuronal physiology. This systematic review focuses on the potential use of glial fibrillary acidic protein (GFAP) as a blood biomarker for the detection of neurological disorders. The review summarizes studies published between January 2012 and September 2021 and highlights the association between elevated GFAP levels and various neurological diseases, suggesting its potential as a valuable diagnostic biomarker.
Astrocytes are the most abundant cell type in the human central nervous system, and they play an important role in the regulation of neuronal physiology. In neurological disorders, astrocyte disintegration leads to the release of glial fibrillary acidic protein (GFAP) from tissue into the bloodstream. Elevated serum levels of GFAP can serve as blood biomarkers, and a useful prognostic tool to facilitate the early diagnosis of several neurological diseases ranging from stroke to neurodegenerative disorders. This systematic review synthesizes studies published be-tween January 2012 and September 2021 that used GFAP as a potential blood biomarker to detect neurological disorders. The following electronic databases were accessed: MEDLINE, Scopus, and Web of Science. In all the databases, the following search strategy was used: 'GFAP'OR 'glial fibrillary acidic protein'AND 'neurological'OR 'neurodegenerative'AND 'plasma'OR s'erum'. The initial search identified 1152 articles. After the exclusion criteria were applied, 48 publications that reported GFAP levels in neurological disorders were identified. A total of 16 different neurological disorders that have plasmatic GFAP levels as a possible biomarker for the disease were described in the articles, being: multiple sclerosis, frontotemporal lobar degeneration, Alzheimer's disease, Parkinson disease, COVID-19, epileptic seizures, Wilson Disease, diabetic ketoacidosis, schizophrenia, autism spectrum disorders, major depressive disorder, glioblastoma, spinal cord injury, asthma, neuromyelitis optica spectrum disorder and Friedreich's ataxia. Our review shows an association between GFAP levels and the disease being studied, suggesting that elevated GFAP levels are a potentially valuable diagnostic biomarker in the evaluation of different neurological diseases.

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