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Tenascin-C in patients with central nervous system infections.
Zachariassen, Morten; Thomsen, Martin Munthe; Hillig, Thore; Trier-Petersen, Pelle; Jensen, Andreas Vestergaard; Friis-Hansen, Lennart Jan; Brandt, Christian Thomas.
Affiliation
  • Zachariassen M; Department of Infectious Diseases, Zealand University Hospital, University of Copenhagen, Roskilde, Denmark. Electronic address: morten_zachariassen@hotmail.com.
  • Thomsen MM; Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital, University Hospital Copenhagen, Hillerød, Denmark.
  • Hillig T; Department of Clinical Biochemistry, Nordsjællands Hospital, University Hospital Copenhagen, Hillerød, Denmark.
  • Trier-Petersen P; Department of Infectious Diseases, Zealand University Hospital, University of Copenhagen, Roskilde, Denmark; Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital, University Hospital Copenhagen, Hillerød, Denmark.
  • Jensen AV; Department of Infectious Diseases, Zealand University Hospital, University of Copenhagen, Roskilde, Denmark; Department of Pulmonary and Infectious Diseases, Nordsjællands Hospital, University Hospital Copenhagen, Hillerød, Denmark.
  • Friis-Hansen LJ; Department of Clinical Microbiology, University Hospital Rigshospitalet, University of Copenhagen, Denmark.
  • Brandt CT; Department of Infectious Diseases, Zealand University Hospital, University of Copenhagen, Roskilde, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen Region, Copenhagen, Denmark.
J Neuroimmunol ; 392: 578373, 2024 Jul 15.
Article in En | MEDLINE | ID: mdl-38776710
ABSTRACT

BACKGROUND:

The extracellular matrix protein tenascin-C has been discovered to be an important regulator of the response to tissue injury and repair in cerebrovascular diseases. This study investigated if tenascin-C is released in response to infections in the central nervous system (CNS).

METHODS:

Tenascin-C concentration in the cerebrospinal fluid (CSF) was measured in patients, (>18 years) with and without CNS infections, admitted to a department of infectious diseases in Denmark. CSF tenascin-C was measured on the Meso-scale platform.

RESULTS:

174 patients were included of which 140 were diagnosed with a CNS infection and 34 where this was ruled out (control group). Median CSF tenascin-C levels were significantly higher among patients with bacterial meningitis (147 pg/mL), viral meningitis (33 mg/mL), viral encephalitis (39 pg/mL) and Lyme neuroborreliosis (45 pg/mL) when compared to controls (21 pg/mL). Correlations between tenascin-C and CSF markers of inflammation and age were only moderate.

CONCLUSION:

Levels of CSF tenascin-C are higher among patients with bacterial and viral neuroinfections, already on admission, but exhibit only a modest correlation with baseline indices of neuroinflammation. CSF tenascin-C is highest among patients with bacterial meningitis compared to the other CNS infections. Patients with unfavorable outcomes presented with higher median CSF tenascin-C than their counterparts.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Central Nervous System Infections / Tenascin Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Neuroimmunol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Central Nervous System Infections / Tenascin Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Neuroimmunol Year: 2024 Document type: Article