Proenkephalin Improves Cardio-Renal Risk Prediction in Acute Coronary Syndromes: The KID-ACS Score.

Acute Coronary Syndromes Acute Kidney Injury Mortality Risk Proenkephalin Risk Prediction

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
31 Aug 2024
Historique:
received: 02 05 2024
revised: 07 08 2024
accepted: 24 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 31 8 2024
Statut: aheadofprint

Résumé

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). 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. 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. 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.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
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 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 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 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.

Identifiants

pubmed: 39215600
pii: 7742743
doi: 10.1093/eurheartj/ehae602
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Florian A Wenzl (FA)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.

Peizhi Wang (P)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
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.

Mattia Arrigo (M)

Department of Internal Medicine, Stadtspital Zurich, Zurich, Switzerland.

Jiri Parenica (J)

Internal and Cardiology Department, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czechia.

Donald J L Jones (DJL)

National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.
Leicester Cancer Research Centre and Department of Genetics and Genome Biology, RKCSB, University of Leicester, Leicester, United Kingdom.

Francesco Bruno (F)

Division of Cardiology, Cardiovascular and Thoracic Department, Molinette Hospital, Città della Salute e della Scienza, Turin, Italy.
Royal Brompton and Harefield Hospitals, London, United Kingdom.

Daniel Tarnwski (D)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Oliver Hartmann (O)

SphingoTec GmbH, 16761 Hennigsdorf, Germany.

Lubos Boucek (L)

Department of Laboratory Medicine - Division of Clinical Biochemistry, University Hospital Brno, Brno, Czechia.

Fabian Lang (F)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Slayman Obeid (S)

Division of Cardiology, Department of Medicine, Basel Cantonal Hospital, Basel, Switzerland.

Andreas Schober (A)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Simon Kraler (S)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.

Alexander Akhmedov (A)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.

Florian Kahles (F)

Department of Internal Medicine I, University Hospital Aachen, Pauwelsstraße 30, 52074, Aachen, Germany.

Alexander Schober (A)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Kok Weng Ow (KW)

National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.

Stefano Ministrini (S)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.

Giovanni G Camici (GG)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
Department of Research and Education, University Hospital Zurich, Zurich, Switzerland.

Andreas Bergmann (A)

SphingoTec GmbH, 16761 Hennigsdorf, Germany.

Luca Liberale (L)

First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, 6 viale Benedetto XV, 16132 Genoa, Italy.
IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, L.go R. Benzi 10, 16132 Genoa, Italy.

Jiri Jarkovsky (J)

Institute of Health Information and Statistics of the Czech Republic, Prague, Czechia.
Institute of Biostatistics and Analysis, Faculty of Medicine, Masaryk University, Brno, Czechia.

Victor Schweiger (V)

Department of Cardiology, University Hospital Zurich, Switzerland.

Jatinderpal K Sandhu (JK)

National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.

Arnold von Eckardstein (A)

Institute of Clinical Chemistry, University Hospital Zurich and University of Zuich, Zurich, Switzerland.

Christian Templin (C)

Department of Cardiology, University Hospital Zurich, Switzerland.

Olivier Muller (O)

Service of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.

Tomas Ondrus (T)

Internal and Cardiology Department, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czechia.

Janet-Jacqueline Olic (JJ)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Marco Roffi (M)

Department of Cardiology, Geneva University Hospital, Geneva, Switzerland.

Lorenz Räber (L)

Department of Cardiology, Cardiovascular Center, University Hospital Bern, Bern, Switzerland.

Thong H Cao (TH)

National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC), Leicester, United Kingdom.
Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.

Carsten G Jungbauer (CG)

Department of Internal Medicine II (Cardiology), University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, 93053, Germany.

Leong L Ng (LL)

Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, United Kingdom.
Leicester van Geest Multi-OMICS Facility, University of Leicester, Leicester, United Kingdom.

Alexandre Mebazaa (A)

Université Paris Cité, INSERM UMR-S 942(MASCOT), Paris, France.
Department of Anesthesiology and Critical Care and Burn Unit, Saint-Louis and Lariboisière Hospitals, FHU PROMICE, DMU Parabol, APHP.Nord, Paris, France.

Thomas F Lüscher (TF)

Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
Royal Brompton and Harefield Hospitals, London, United Kingdom.
National Heart and Lung Institute, Imperial College, London, United Kingdom.
School of Cardiovascular Medicine and Sciences, Kings College London, London, United Kingdom.

Classifications MeSH