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dc.contributor.authorÇakır, Murteza
dc.contributor.authorÇalıkoğlu, Çağatay
dc.contributor.authorYılmaz, Atilla
dc.contributor.authorAkpınar, Erol
dc.contributor.authorBayraktutan, Zafer
dc.contributor.authorTopçu, Atilla
dc.date.accessioned2020-12-19T19:49:40Z
dc.date.available2020-12-19T19:49:40Z
dc.date.issued2017
dc.identifier.citationCakir, M., Calikoglu, C., Yılmaz, A., Akpinar, E., Bayraktutan, Z., & Topcu, A. (2017). Serum nesfatin-1 levels: a potential new biomarker in patients with subarachnoid hemorrhage. The International journal of neuroscience, 127(2), 154–160. https://doi.org/10.3109/00207454.2016.1153473en_US
dc.identifier.issn0020-7454
dc.identifier.issn1563-5279
dc.identifier.urihttps://doi.org/10.3109/00207454.2016.1153473
dc.identifier.urihttps://hdl.handle.net/11436/2321
dc.descriptionAnnual Meeting of the Congress-of-Neurological-Surgeons (CNS) -- SEP 26-30, 2015 -- New Orleans, LAen_US
dc.descriptionWOS: 000389642100007en_US
dc.descriptionPubMed: 26872406en_US
dc.description.abstractBackground: Acute subarachnoid hemorrhage (SAH) is a neurological emergency with significant potential for long-term morbidity and mortality. Nesfatin-1 is a polypeptide which is found in various regions of the brain that play role in the feeding and metabolic regulation. Objective: So this study aimed to investigate if nesfatin-1 levels in patients with SAH, could be used as a marker for the severity and prognosis. Method: Forty-eight consecutive patients (except those excluded) admitted to the emergency service of our hospital and hospitalized at our clinic with the diagnosis of aneurysmal SAH between 2011 and 2013 were included in the study and followed up for six months for outcome. the control group consisted of 48 healthy individuals of similar age and gender. Results: During the 6-month follow-up, 7 of 48 patients died and 16 (33.3%) patients had poor Glasgow Outcome Score (GOS) scores. in the study group, themean nesfatin-1 level was significantly higher than the control group (7.36 +/- 2.5 pg/ml and 4.29 +/- 2.02 pg/ml, respectively; p < 0.01). the mean nesfatin-1 level was 11.58 +/- 0.87 pg/ml in the non-survival group and 6.64 +/- 1.89 pg/ml in the survival group. Furthermore, it was 10.22 +/- 1.42 pg/ml in patients with poor outcome in terms of GOS and 5.93 +/- 1.46 pg/ml in those with good outcome. the nesfatin-1 levels significantly increased with worsening of GOS, the World Federation of Neurological Surgeons grading system, and Fisher scores and increasing plasma C-reactive protein levels (p < 0.01 for all). Conclusion: the present study is the first that shows the mortality/poor outcome of the SAH with assessing serum nesfatin-1 levels. So levels of nesfatin-1 might be useful in SAH management.en_US
dc.description.sponsorshipCongress Neurol Surgen_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSubarachnoid hemorrhageen_US
dc.subjectNesfatin-1en_US
dc.subjectGlasgow Coma Score (GCS)en_US
dc.titleSerum nesfatin-1 levels: a potential new biomarker in patients with subarachnoid hemorrhageen_US
dc.typeconferenceObjecten_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorTopçu, Atilla
dc.identifier.doi10.3109/00207454.2016.1153473
dc.identifier.volume127en_US
dc.identifier.issue2en_US
dc.identifier.startpage154en_US
dc.identifier.endpage160en_US
dc.relation.journalInternational Journal of Neuroscienceen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US


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