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Proenkephalin Improves Cardio-Renal Risk Prediction in Acute Coronary Syndromes: The KID-ACS Score.
Wenzl, Florian A; Wang, Peizhi; Arrigo, Mattia; Parenica, Jiri; Jones, Donald J L; Bruno, Francesco; Tarnwski, Daniel; Hartmann, Oliver; Boucek, Lubos; Lang, Fabian; Obeid, Slayman; Schober, Andreas; Kraler, Simon; Akhmedov, Alexander; Kahles, Florian; Schober, Alexander; Ow, Kok Weng; Ministrini, Stefano; Camici, Giovanni G; Bergmann, Andreas; Liberale, Luca; Jarkovsky, Jiri; Schweiger, Victor; Sandhu, Jatinderpal K; von Eckardstein, Arnold; Templin, Christian; Muller, Olivier; Ondrus, Tomas; Olic, Janet-Jacqueline; Roffi, Marco; Räber, Lorenz; Cao, Thong H; Jungbauer, Carsten G; Ng, Leong L; Mebazaa, Alexandre; Lüscher, Thomas F.
Afiliación
  • Wenzl FA; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Wang P; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Arrigo M; Department of Cardiology, National Clinical Research Center for Cardiovascular Diseases, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Parenica J; Department of Internal Medicine, Stadtspital Zurich, Zurich, Switzerland.
  • Jones DJL; Internal and Cardiology Department, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czechia.
  • Bruno F; National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
  • Tarnwski D; Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
  • Hartmann O; Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.
  • Boucek L; Leicester Cancer Research Centre and Department of Genetics and Genome Biology, RKCSB, University of Leicester, Leicester, United Kingdom.
  • Lang F; Division of Cardiology, Cardiovascular and Thoracic Department, Molinette Hospital, Città della Salute e della Scienza, Turin, Italy.
  • Obeid S; Royal Brompton and Harefield Hospitals, London, United Kingdom.
  • Schober A; Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.
  • Kraler S; SphingoTec GmbH, 16761 Hennigsdorf, Germany.
  • Akhmedov A; Department of Laboratory Medicine - Division of Clinical Biochemistry, University Hospital Brno, Brno, Czechia.
  • Kahles F; Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.
  • Schober A; Division of Cardiology, Department of Medicine, Basel Cantonal Hospital, Basel, Switzerland.
  • Ow KW; Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.
  • Ministrini S; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Camici GG; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Bergmann A; Department of Internal Medicine I, University Hospital Aachen, Pauwelsstraße 30, 52074, Aachen, Germany.
  • Liberale L; Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.
  • Jarkovsky J; National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
  • Schweiger V; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Sandhu JK; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • von Eckardstein A; Department of Research and Education, University Hospital Zurich, Zurich, Switzerland.
  • Templin C; SphingoTec GmbH, 16761 Hennigsdorf, Germany.
  • Muller O; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, 6 viale Benedetto XV, 16132 Genoa, Italy.
  • Ondrus T; IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, L.go R. Benzi 10, 16132 Genoa, Italy.
  • Olic JJ; Institute of Health Information and Statistics of the Czech Republic, Prague, Czechia.
  • Roffi M; Institute of Biostatistics and Analysis, Faculty of Medicine, Masaryk University, Brno, Czechia.
  • Räber L; Department of Cardiology, University Hospital Zurich, Switzerland.
  • Cao TH; National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
  • Jungbauer CG; Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
  • Ng LL; Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.
  • Mebazaa A; Institute of Clinical Chemistry, University Hospital Zurich and University of Zuich, Zurich, Switzerland.
  • Lüscher TF; Department of Cardiology, University Hospital Zurich, Switzerland.
Eur Heart J ; 2024 Aug 31.
Article en En | MEDLINE | ID: mdl-39215600
ABSTRACT
BACKGROUND AND

AIMS:

Circulating proenkephalin (PENK) is a stable endogenous polypeptide with fast response to glomerular dysfunction and tubular damage. This study examined the predictive value of PENK for renal outcomes and mortality in patients with acute coronary syndromes (ACS).

METHODS:

Proenkephalin was measured in plasma in a prospective multicentre ACS cohort from Switzerland (n=4787) and in validation cohorts from the UK (n=1141), Czechia (n=927), and Germany (n=220). A biomarker-enhanced risk score (KID-ACS score) for simultaneous prediction of in-hospital acute kidney injury (AKI) and 30-day mortality was derived and externally validated.

RESULTS:

On multivariable adjustment for established risk factors, circulating PENK remained associated with in-hospital AKI (per log2 increase adjusted odds ratio [OR] 1.53, 95% confidence interval [CI] 1.13-2.09, P=0.007) and 30-day mortality (adjusted hazard ratio [HR] 2.73, 95% CI 1.85-4.02, P<0.001). The KID-ACS score integrates PENK and showed an area under the receiver operating characteristic curve (AUC) of 0.72 (95% CI 0.68-0.76) for in-hospital AKI, and of 0.91 (95% CI 0.87-0.95) for 30-day mortality in the derivation cohort. Upon external validation, KID-ACS achieved similarly high performance for in-hospital AKI (Zurich AUC 0.73, 95% CI 0.70-0.77; Czechia AUC 0.75, 95% CI 0.68-0.81; Germany AUC 0.71, 95% CI 0.55-0.87) and 30-day mortality (UK AUC 0.87, 95% CI 0.83-0.91; Czechia AUC 0.91, 95% CI 0.87-0.94; Germany AUC 0.96, 95% CI 0.92-1.00) outperforming the CA-AKI score and the GRACE 2.0 score, respectively.

CONCLUSIONS:

Circulating PENK offers incremental value for predicting in-hospital AKI and mortality in ACS. The simple 6-item KID-ACS risk score integrates PENK and provides a novel tool for simultaneous assessment of renal and mortality risk in patients with ACS.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Eur Heart J Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Eur Heart J Año: 2024 Tipo del documento: Article País de afiliación: Suiza