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               <mods:name>
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                  <mods:namePart>Cediel, Germán</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Rueda, Ferran</mods:namePart>
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                  <mods:namePart>Oliveras, Teresa</mods:namePart>
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                  <mods:namePart>Labata, Carlos</mods:namePart>
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                  <mods:namePart>Ferrer Massot, Marc</mods:namePart>
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                  <mods:namePart>Aranda-Nevado, M. Cruz</mods:namePart>
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                  <mods:namePart>Serra-Gregori, Judith</mods:namePart>
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                  <mods:namePart>Núñez, Julio</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Garcia Garcia, Cosme</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Bayés-Genís, Antoni</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Universitat Autònoma de Barcelona</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2018</mods:dateIssued>
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               <mods:abstract>Altres ajuts: Fundació La MARATÓ de TV3 (201502 and 201516)The aim of the present study was to evaluate the prognostic value of the Stanniocalcin-2/PAPP-A/IGFBP-4 axis in patients with ST-segment elevation myocardial infarction (STEMI). Observational cohort study performed in 1085 consecutive STEMI patients treated with early reperfusion between February 2011 and August 2014. Stanniocalcin-2, PAPP-A, and IGFBP-4 were measured using state-of-the art immunoassays. The primary outcome was the composite endpoint of all-cause mortality and readmission due to heart failure (HF). Median follow-up was 3.3 years (IQR 1.0-3.7), during which 176 patients (16.2%) presented a composite endpoint. Multivariable cox regression analysis revealed that Stanniocalcin-2 (HR 2.06; 95% CI 1.13-3.75; p = 0.018), IGFBP-4 (HR 1.73; 95% CI 1.14-2.64; p = 0.010), Killip-Kimball class III-IV (HR 1.40; 95% CI 1.13-1.74; p = 0.002), NT-ProBNP (HR 1.21; 95% CI 1.07-1.37; p = 0.002), age (HR 1.06; 95% CI 1.04-1.08; p &lt; 0.001) and left ventricular ejection fraction (HR 0.97; 95% CI 0.95-0.98; p &lt; 0.001) were independent predictors of the composite endpoint. A model containing Stanniocalcin-2 and IGFBP-4 on top of clinical variables significantly improved C-index discrimination (p = 0.036). Stanniocalcin-2 was also identified as independent predictor of all-cause mortality (HR 2.23; 95% CI 1.16-4.29; p = 0.017) and readmission due to HF (HR 3.42; 95% CI 1.22-9.60; p = 0.020). In STEMI patients, Stanniocalcin-2 and IGFBP-4 emerged as independent predictors of all-cause death and readmission due to HF. The Stanniocalcin-2/PAPP-A/IGFBP-4 axis exhibits a significant role in STEMI risk stratification.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
               <mods:subject>
                  <mods:topic>STEMI</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Prognosis</mods:topic>
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               <mods:subject>
                  <mods:topic>Stanniocalcin-2</mods:topic>
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                  <mods:topic>PAPP-A</mods:topic>
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                  <mods:topic>IGFBP-4</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Prognostic value of the Stanniocalcin-2/PAPP-A/IGFBP-4 axis in ST-segment elevation myocardial infarction</mods:title>
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