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                  <mods:namePart>Pascual-Figal, Domingo A</mods:namePart>
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                  <mods:namePart>Díez, Javier</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Roche</mods:namePart>
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                  <mods:namePart>Novartis</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2020-04-08T13:52:12Z</mods:dateAccessioned>
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               <mods:identifier type="citation">J Am Coll Cardiol. 2019; 73(9):1016-1025</mods:identifier>
               <mods:identifier type="doi">10.1016/j.jacc.2018.11.054</mods:identifier>
               <mods:identifier type="e-issn">1558-3597</mods:identifier>
               <mods:identifier type="issn">073-1097</mods:identifier>
               <mods:identifier type="journal">Journal of the American College of Cardiology</mods:identifier>
               <mods:identifier type="pubmedID">30846095</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/9492</mods:identifier>
               <mods:abstract>BACKGROUND: Soluble ST2 (sST2), which is the soluble form of interleukin (IL)-1 receptor-like 1, identifies risk in acutely decompensated heart failure (ADHF). IL-1β is an inflammatory cytokine that has deleterious effects in myocardial remodeling and function. IL-1β inhibition has beneficial effects after acute myocardial infarction. However, the role of IL-1β in ADHF and its relationship to ST2 remain unclear. OBJECTIVES: This study sought to investigate the relationship between IL-1β and sST2, and the prognostic impact of such a relationship in patients with ADHF. METHODS: This study examined 316 consecutive patients who were hospitalized with ADHF (72 ± 12 years of age, 57% male, and left ventricular ejection fraction 45 ± 17%). Blood samples were collected at presentation, and IL-1β and sST2 levels were measured. All-cause mortality was obtained for all patients at 1 year. RESULTS: The IL-1β concentration at presentation was associated with prior HF hospitalizations, functional impairment, and higher N-terminal pro-B-type natriuretic peptide and high-sensitivity troponin T concentrations. IL-1β was higher in patients who died during the year after hospitalization (n = 52, 16.5%) (p = 0.005), and the optimal threshold was identified with levels over 49.1 pg/ml (hazard ratio: 2.5; 95% confidence interval: 1.43 to 4.49; p = 0.0014). Circulating IL-1β positively correlated with sST2 (ρ = 0.65; p &lt; 0.001). Considering the prognostic thresholds of IL-1β (≥49.1 pg/ml) and sST2 (≥35.0 ng/ml) concentrations: all patients with low sST2 also presented with low IL-1β; among patients with high sST2, only those with also high IL-1β had a significantly higher risk of death (30% vs. 14%; hazard ratio: 2.52; 95% confidence interval: 1.40 to 4.56; p = 0.002). CONCLUSIONS: Circulating IL-1β concentrations are clinically meaningful in ADHF patients and interplay with the predictive ability of sST2. IL-1 axis-related inflammation signaling may represent a therapeutic target in ADHF.</mods:abstract>
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               <mods:subject>
                  <mods:topic>IL-1β</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>ST2</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Acute</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Heart failure</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Interleukin-1</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>The Interleukin-1 Axis and Risk of Death in Patients With Acutely Decompensated Heart Failure</mods:title>
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               <mods:genre>journal article</mods:genre>
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