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Neuroinflammation Is Associated with GFAP and sTREM2 Levels in Multiple Sclerosis

Authors :
Federica Azzolini
Luana Gilio
Luigi Pavone
Ennio Iezzi
Ettore Dolcetti
Antonio Bruno
Fabio Buttari
Alessandra Musella
Georgia Mandolesi
Livia Guadalupi
Roberto Furlan
Annamaria Finardi
Teresa Micillo
Fortunata Carbone
Giuseppe Matarese
Diego Centonze
Mario Stampanoni Bassi
Source :
Biomolecules, Vol 12, Iss 2, p 222 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Background: Astrocytes and microglia play an important role in the inflammatory process of multiple sclerosis (MS). We investigated the associations between the cerebrospinal fluid (CSF) levels of glial fibrillary acid protein (GFAP) and soluble triggering receptors expressed on myeloid cells-2 (sTREM-2), inflammatory molecules, and clinical characteristics in a group of patients with relapsing-remitting MS (RRMS). Methods: Fifty-one RRMS patients participated in the study. Clinical evaluation and CSF collection were performed at the time of diagnosis. The CSF levels of GFAP, sTREM-2, and of a large set of inflammatory and anti-inflammatory molecules were determined. MRI structural measures (cortical thickness, T2 lesion load, cerebellar volume) were examined. Results: The CSF levels of GFAP and sTREM-2 showed significant correlations with inflammatory cytokines IL-8, G-CSF, and IL-5. Both GFAP and sTREM-2 CSF levels positively correlated with age at diagnosis. GFAP was also higher in male MS patients, and was associated with an increased risk of MS progression, as evidenced by higher BREMS at the onset. Finally, a negative association was found between GFAP CSF levels and cerebellar volume in RRMS at diagnosis. Conclusions: GFAP and sTREM-2 represent suitable biomarkers of central inflammation in MS. Our results suggest that enhanced CSF expression of GFAP may characterize patients with a higher risk of progression.

Details

Language :
English
ISSN :
12020222 and 2218273X
Volume :
12
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Biomolecules
Publication Type :
Academic Journal
Accession number :
edsdoj.2db5546a609f491d87bf82b8ef3ce066
Document Type :
article
Full Text :
https://doi.org/10.3390/biom12020222