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Serum sTREM2 Levels and Disability Progression in Patients With Primary Progressive Multiple Sclerosis

Articolo
Data di Pubblicazione:
2026
Citazione:
Serum sTREM2 Levels and Disability Progression in Patients With Primary Progressive Multiple Sclerosis / Fissolo, N.; Benkert, P.; Vilaseca-Jolonch, A.; Blanco, Y.; Hegen, H.; Berek, K.; Perez-Miralles, F.; Rejdak, K.; Villar, L.; Monreal, E.; Alvarez-Lafuente, R.; Bachhuber, F.; Tumani, H.; Martinez-Yelamos, S.; Sanchez-Lopez, A.; Garcia-Merino, A.; Gutierrez, L.; Castillo-Trivino, T.; Lycke, J.; Rosenstein, I.; Tellez, N.; Furlan, R.; Lunemann, J. D.; Khalil, M.; Kuhle, J.; Montalban, X.; Comabella, M.. - In: EUROPEAN JOURNAL OF NEUROLOGY. - ISSN 1351-5101. - 33:2(2026). [10.1111/ene.70480]
Abstract:
Background: Triggering receptor expressed on myeloid cells 2 (TREM2) is a microglia surface receptor that aids in tissue repair and debris clearance. The soluble form, sTREM2, found in both blood and cerebrospinal fluid, is considered a biomarker for microglial activation. Based on the central role of microglia in MS pathogenesis, we aimed to investigate whether serum sTREM2 levels could predict disability progression in patients with primary progressive MS. Methods: Serum levels of sTREM2 were measured at baseline using a single-molecule array assay in a multicenter cohort of 137 primary progressive multiple sclerosis (PPMS) patients. Univariable and multivariable linear models evaluated the association between sTREM2 levels and EDSS change at 2 years, 6 years, and last follow-up. Results: While an association was observed at 2 years only in non-inflammatory PPMS patients, no consistent relationship was found between sTREM2 levels and disability progression over longer follow-up. Conclusions: These findings suggest that serum sTREM2 may have limited value as a biomarker of disability progression in PPMS.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
biomarkers; disability progression; primary progressive multiple sclerosis; sTREM2
Elenco autori:
Fissolo, N.; Benkert, P.; Vilaseca-Jolonch, A.; Blanco, Y.; Hegen, H.; Berek, K.; Perez-Miralles, F.; Rejdak, K.; Villar, L.; Monreal, E.; Alvarez-Lafuente, R.; Bachhuber, F.; Tumani, H.; Martinez-Yelamos, S.; Sanchez-Lopez, A.; Garcia-Merino, A.; Gutierrez, L.; Castillo-Trivino, T.; Lycke, J.; Rosenstein, I.; Tellez, N.; Furlan, R.; Lunemann, J. D.; Khalil, M.; Kuhle, J.; Montalban, X.; Comabella, M.
Autori di Ateneo:
FURLAN ROBERTO
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/202297
Pubblicato in:
EUROPEAN JOURNAL OF NEUROLOGY
Journal
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