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Increased level of LIGHT/TNFSF14 is associated with survival in aneurysmal subarachnoid hemorrhage

Schranz, Daniel (författare)
Department of Neurology, University of Pecs, Medical School, Pecs, Hungary
Molnar, Tihamer (författare)
Department of Anaesthesiology and Intensive Care, University of Pecs, Medical School, Pecs, Hungary
Erdo‐Bonyar, Szabina (författare)
Department of Immunology and Biotechnology, University of Pecs, Medical School, Pecs, Hungary
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Simon, Diana (författare)
Department of Immunology and Biotechnology, University of Pecs, Medical School, Pecs, Hungary
Berki, Tímea (författare)
Department of Immunology and Biotechnology, University of Pecs, Medical School, Pecs, Hungary
Nagy, Csaba (författare)
Department of Neurosurgery, University of Pecs, Medical School, Pecs, Hungary
Czeiter, Endre (författare)
Department of Neurosurgery, University of Pecs, Medical School, Pecs, Hungary; Neurotrauma Research Group, Szentágothai Research Centre, University of Pécs, Pécs, Hungary; MTA‐PTE Clinical Neuroscience, MR Research Group, Pécs, Hungary
Büki, Andras, 1966- (författare)
Department of Neurosurgery, University of Pecs, Medical School, Pecs, Hungary
Lenzser, Gabor (författare)
Department of Neurosurgery, University of Pecs, Medical School, Pecs, Hungary
Csecsei, Peter (författare)
Department of Neurosurgery, University of Pecs, Medical School, Pecs, Hungary
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 (creator_code:org_t)
2021-01-25
2021
Engelska.
Ingår i: Acta Neurologica Scandinavica. - : John Wiley & Sons. - 0001-6314 .- 1600-0404. ; 143:5, s. 530-537
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objectives: Multiple cytokines have been implicated in aneurysmal subarachnoid hemorrhage (aSAH), but tumor necrosis factor superfamily 14 (LIGHT/TNFSF14) and oncostatin-M (OSM) have not been previously explored.Aims of the study: The primary objective of this study was to examine the relationship between TNFSF14 and OSM levels and survival. Our secondary goal was to investigate a potential association between these markers and the incidence of delayed cerebral ischemia (DCI).Materials & methods: We consecutively recruited 60 patients with a clinical diagnosis of aSAH. LIGHT/TNFSF14 and OSM serum concentrations were determined by ELISA. The primary endpoint was survival at Day 30, while development of DCI was assessed as secondary outcome.Results: Patients had significantly higher levels of both markers than the control group (median of LIGHT: 18.1 pg/ml vs. 7 pg/ml; p = 0.01; median of OSM: 10.3 pg/ml vs. 2.8 pg/ml, p < 0.001). Significantly lower serum level of LIGHT/TNFSF14 was found in nonsurviving patients (n = 9) compared with survivors (n = 51; p = 0.011). Based on ROC analysis, serum LIGHT/TNFSF14 with a cutoff value of >7.95 pg/ml predicted 30-day survival with a sensitivity of 71% and specificity of 78% (Area: 0.763; 95% CI: 0.604-0.921, p = 0.013). In addition, it was also a predictor of DCI with a sensitivity of 72.7% and a specificity of 62.5% (AUC: 0.702; 95% CI: 0.555-0.849, p = 0.018). Based on binary logistic regression analysis, LIGHT/TNFSF14 was found to be independently associated with 30-day mortality, but not with DCI.Conclusion: In this cohort, a higher serum level of LIGHT/TNFSF14 was associated with increased survival of patients with aSAH.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

LIGHT
TNFSF14
mortality
subarachnoid hemorrhage

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