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dc.contributor.authorSahin, B. E.
dc.contributor.authorÇelikbilek, A.
dc.contributor.authorKoçak, Y.
dc.contributor.authorSaltoğlu, G. T.
dc.contributor.authorKonar, N. M.
dc.contributor.authorHızmalı, L.
dc.date.accessioned2022-12-22T08:56:06Z
dc.date.available2022-12-22T08:56:06Z
dc.date.issued2022en_US
dc.identifier.citationSahin, B. E., Celikbilek, A., Kocak, Y., Saltoglu, G. T., Konar, N. M., & Hizmali, L. (2022). Plasma biomarkers of brain injury in COVID-19 patients with neurological symptoms. Journal of the Neurological Sciences, 439, 120324.en_US
dc.identifier.issn0022-510X
dc.identifier.issn1878-5883
dc.identifier.urihttps://doi.org/10.1016/j.jns.2022.120324
dc.identifier.urihttps://hdl.handle.net/20.500.12513/4857
dc.description.abstractObjective: Neurological symptoms (NS) were often reported in COVID-19 infection. We examined the plasma levels of glial fibrillary acidic protein (GFAP) and S100B together, as brain injury biomarkers, in relation to persistent NS in a cohort of patients with COVID-19 during the acute phase of the disease.Methods: A total of 20 healthy controls and 58 patients with confirmed COVID-19 were enrolled in this prospective study. Serum GFAP and S100B levels were measured by using enzymle linked immunoassay method from blood samples.Results: Serum GFAP levels were found to be significantly higher in the severe group than in the controls (p = 0.007). However, serum S100B levels were similar between control and disease groups (p > 0.05). No significant results for GFAP and S100B were obtained between the disease groups depending on whether the sampling time was below or above 5 days (p > 0.05). We did not find a correlation between serum GFAP and S100B levels and the presence of NS (p > 0.05). However, serum S100B levels were slightly higher in patients with multiple NS than in those with a single symptom (p = 0.044).Conclusions: Elevated GFAP was associated with disease severity but not with NS in COVID-19 patients. Whereas, high serum S100B was associated with the multipl NS in these patients. Our data suggest that GFAP and S100B may be of limited value currently in order to represent the neuronal damage, though serving a basis for the future work.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.jns.2022.120324en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectSARS-CoV-2en_US
dc.subjectCOVID-19en_US
dc.subjectBrain injuryen_US
dc.subjectGFAPen_US
dc.subjectS100Ben_US
dc.subjectNeurological symptomsen_US
dc.titlePlasma biomarkers of brain injury in COVID-19 patients with neurological symptomsen_US
dc.typearticleen_US
dc.relation.journalJournal Of The Neurological Sciencesen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorIDBurç Esra Şahin/ 0000-0003-1008-2743en_US
dc.identifier.volume439en_US
dc.identifier.startpage1en_US
dc.identifier.endpage6en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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