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dc.contributor.authorGul, Ibrahim
dc.contributor.authorYucel, Oguzhan
dc.contributor.authorZararsiz, Abdullah
dc.contributor.authorDemirpence, Ozlem
dc.contributor.authorYucel, Hasan
dc.contributor.authorZorlu, Ali
dc.contributor.authorYilmaz, Mehmet Birhan
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:40:34Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:40:34Z
dc.date.issued2017
dc.identifier.issn2149-2263
dc.identifier.issn2149-2271
dc.identifier.urihttps://dx.doi.org/10.14744/AnatolJCardiol.2017.7741
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6697
dc.descriptionWOS: 000414037000009en_US
dc.descriptionPubMed ID: 28761021en_US
dc.description.abstractObjective: Soluble suppression of tumorigenicity-2 (sST2), a member of the interleukin 1 receptor family, is increased in mechanical stress conditions and is produced by cardiomyocytes and cardiac fibroblasts. Elevated sST2 level is associated with the prognosis of acute coronary syndrome, pulmonary arterial hypertension, and acute and chronic heart failure (HF). In this study, we aimed to investigate the relationship between sST2 levels and cardiovascular mortality in outpatients with HF. Methods: This study used a prospective observational cohort design. A total of 130 consecutive outpatients with HF were prospectively evaluated. Clinical characteristics, laboratory results, cardiovascular risk factors, comorbidities, and medication use were recorded. The patients were followed up for a mean period of 12 +/- 4 months for the development of cardiovascular death. They were classified into two groups: those who survived and those who died. Results: Mean age of patients was 67 +/- 11 years (69% males). After follow-up, 23 of 130 patients (18%) experienced cardiovascular death. sST2 levels were higher among those who died compared with among those who survived [51 (21-162) vs. 27 (9-198) ng/mL, p<0.001]. Optimal cut-off sST2 level to predict cardiovascular mortality was found to be >30 ng/mL with a sensitivity of 87% and a specificity of 67% (AUC = 0.808, 95% CI=0.730 to 0.872). sST2 levels were negatively correlated with left ventricular ejection fraction and triglyceride, total cholesterol, LDL cholesterol, and hemoglobin levels and were positively correlated with left atrium size and the presence of right ventricular dilatation. In multiple Cox regression analysis, sST2 level of >30 ng/mL (HR=6.756, p=0.002, 95% CI=1.983-23.018), hemoglobin level (HR=0.705, p<0.001, 95% CI=0.587-0.847), age (HR=1.050, p=0.013, 95% CI=1.010-1.091), and HDL cholesterol level (HR=0.936, p=0.010, 95% CI=0.889-0.984) remained to be associated with an increased risk of mortality. Conclusion: sST2 measurement could help risk stratification in outpatients with HF. Moreover, this is the first study describing the impact of sST2 protein in Turkish patients with HF.en_US
dc.language.isoengen_US
dc.publisherTURKISH SOC CARDIOLOGYen_US
dc.relation.isversionof10.14744/AnatolJCardiol.2017.7741en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectsoluble suppression of tumorigenicity-2en_US
dc.subjectheart failureen_US
dc.subjectcardiovascular mortalityen_US
dc.titlePrognostic role of soluble suppression of tumorigenicity-2 on cardiovascular mortality in outpatients with heart failureen_US
dc.typearticleen_US
dc.relation.journalANATOLIAN JOURNAL OF CARDIOLOGYen_US
dc.contributor.department[Gul, Ibrahim -- Zararsiz, Abdullah -- Yucel, Hasan -- Zorlu, Ali -- Yilmaz, Mehmet Birhan] Cumhuriyet Univ, Fac Med, Dept Cardiol, Sivas, Turkey -- [Demirpence, Ozlem] Cumhuriyet Univ, Fac Med, Dept Biochem, Sivas, Turkey -- [Yucel, Oguzhan] Samsun Educ & Res Hosp, Dept Cardiol, Samsun, Turkeyen_US
dc.contributor.authorIDYILMAZ, Mehmet Birhan -- 0000-0002-8169-8628; YILMAZ, MEHMET BIRHAN -- 0000-0002-8169-8628en_US
dc.identifier.volume18en_US
dc.identifier.issue3en_US
dc.identifier.endpage205en_US
dc.identifier.startpage200en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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