Copeptin, Natriuretic Peptides, and Cardiovascular Outcomes in Patients With CKD: The German Chronic Kidney Disease (GCKD) Study.

Copeptin MR-pro-ANP NT-pro-BNP biomarkers cardiac diseases chronic kidney disease heart failure kidney diseases

Journal

Kidney medicine
ISSN: 2590-0595
Titre abrégé: Kidney Med
Pays: United States
ID NLM: 101756300

Informations de publication

Date de publication:
Nov 2023
Historique:
medline: 2 11 2023
pubmed: 2 11 2023
entrez: 2 11 2023
Statut: epublish

Résumé

Copeptin and Midrange pro-atrial natriuretic peptide (MR-pro-ANP) are associated with outcomes independently of N-terminal pro-brain natriuretic peptide (NT-pro-BNP) in patients with heart failure (HF). The value of these markers in patients with chronic kidney disease (CKD) has not been studied. Prospective cohort study. A total of 4,417 patients enrolled in the German Chronic Kidney Disease (GCKD) study with an estimated glomerular filtration rate of 30-60 mL/min/1.73m Copeptin, MR-pro-ANP, and NT-pro-BNP levels were measured in baseline samples. Noncardiovascular death, cardiovascular (CV) death, major adverse CV event (MACE), and hospitalization for HF. HRs for associations of Copeptin, MR-pro-ANP, and NT-pro-BNP with outcomes were estimated using Cox regression analyses adjusted for established risk factors. During a maximum follow-up of 6.5 years, 413 non-CV deaths, 179 CV deaths, 519 MACE, and 388 hospitalizations for HF were observed. In Cox regression analyses adjusted for established risk factors, each one of the 3 markers were associated with all the 4 outcomes, albeit the highest HRs were found for NT-pro-BNP. When models were extended to include all the 3 markers, NT-pro-BNP remained associated with all 4 outcomes. Conversely, from the 2 novel markers, associations remained only for Copeptin with non-CV death (HR, 1.62; 95% CI, 1.04-2.54 for highest vs lowest quintile) and with hospitalizations for HF (HR, 1.73; 95% CI, 1.08-2.75). Single-point measurements of Copeptin, MR-pro-ANP, and NT-pro-BNP. In patients with moderately severe CKD, we confirm NT-pro-BNP to be strongly associated with all outcomes examined. As the main finding, the novel marker Copeptin demonstrated independent associations with non-CV death and hospitalizations for HF, and should therefore be evaluated further for risk assessment in CKD. A blood sample-based biomarker that indicates high cardiovascular risk in a patient with kidney disease would help to guide interventions and has the potential to improve outcomes. In 4,417 patients of the German Chronic Kidney Disease study, we assessed the relationship of Copeptin, pro-atrial natriuretic peptide, and N-terminal pro-brain natriuretic peptide (NT-pro-BNP) with important outcomes over a follow-up period of 6.5 years. NT-pro-BNP was strongly associated with all of the 4 outcomes, including death unrelated to cardiovascular disease, death because of cardiovascular disease, a major cardiovascular event, and hospitalization for heart failure. Copeptin was associated with death unrelated to cardiovascular disease and hospitalization for heart failure. NT-pro-BNP and Copeptin are, therefore, promising candidates for a blood sample-based strategy to identify patients with kidney disease at high cardiovascular risk.

Identifiants

pubmed: 37915964
doi: 10.1016/j.xkme.2023.100725
pii: S2590-0595(23)00143-7
pmc: PMC10616426
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100725

Investigateurs

Kai-Uwe Eckardt (KU)
Heike Meiselbach (H)
Mario Schiffer (M)
Hans-Ulrich Prokosch (HU)
Barbara Bärthlein (B)
Andreas Beck (A)
André Reis (A)
Arif B Ekici (AB)
Susanne Becker (S)
Dinah Becker-Grosspitsch (D)
Ulrike Alberth-Schmidt (U)
Birgit Hausknecht (B)
Anke Weigel (A)
Gerd Walz (G)
Anna Köttgen (A)
Ulla T Schultheiß (UT)
Fruzsina Kotsis (F)
Simone Meder (S)
Erna Mitsch (E)
Ursula Reinhard (U)
Jürgen Floege (J)
Turgay Saritas (T)
Elke Schaeffner (E)
Seema Baid-Agrawal (S)
Kerstin Theisen (K)
Hermann Haller (H)
Jan Menne (J)
Martin Zeier (M)
Claudia Sommerer (C)
Johanna Theilinger (J)
Gunter Wolf (G)
Martin Busch (M)
Rainer Paul (R)
Thomas Sitter (T)
Christoph Wanner (C)
Vera Krane (V)
Antje Börner-Klein (A)
Britta Bauer (B)
Florian Kronenberg (F)
Julia Raschenberger (J)
Barbara Kollerits (B)
Lukas Forer (L)
Sebastian Schönherr (S)
Hansi Weissensteiner (H)
Peter Oefner (P)
Wolfram Gronwald (W)
Matthias Schmid (M)
Jennifer Nadal (J)

Informations de copyright

© 2023 The Authors.

Références

Nephrol Dial Transplant. 2015 Mar;30(3):441-51
pubmed: 25271006
N Engl J Med. 2020 Oct 8;383(15):1436-1446
pubmed: 32970396
J Am Heart Assoc. 2017 Jul 5;6(7):
pubmed: 28679558
Clin Chem. 2017 May;63(5):997-1007
pubmed: 28280053
J Card Fail. 2012 May;18(5):351-8
pubmed: 22555263
N Engl J Med. 2023 Jan 12;388(2):117-127
pubmed: 36331190
Am J Kidney Dis. 2021 Nov;78(5):669-677.e1
pubmed: 33839201
J Am Soc Nephrol. 2011 Apr;22(4):782-90
pubmed: 21415158
Nephrol Dial Transplant. 2012 Apr;27(4):1454-60
pubmed: 21862458
Int J Cardiol. 2016 Oct 15;221:327-32
pubmed: 27404700
Biometrics. 2002 Mar;58(1):1-12
pubmed: 11890304
BMC Geriatr. 2022 Mar 21;22(1):230
pubmed: 35313808
Arterioscler Thromb Vasc Biol. 2014 Aug;34(8):1770-7
pubmed: 24876355
J Am Coll Cardiol. 2006 Oct 17;48(8):1621-7
pubmed: 17045898
Eur J Endocrinol. 2014 Dec;171(6):737-42
pubmed: 25249697
Ann Intern Med. 2009 May 5;150(9):604-12
pubmed: 19414839
N Engl J Med. 2020 Dec 03;383(23):2219-2229
pubmed: 33264825
Clin Chem. 2006 Jan;52(1):112-9
pubmed: 16269513
ESC Heart Fail. 2018 Apr;5(2):288-296
pubmed: 29476612
J Am Coll Cardiol. 2007 Nov 13;50(20):1973-80
pubmed: 17996563
Lancet. 2018 Nov 10;392(10159):2052-2090
pubmed: 30340847

Auteurs

Markus P Schneider (MP)

Department of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.

Matthias Schmid (M)

Department of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.

Jennifer Nadal (J)

Department of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.

Vera Krane (V)

Department of Medicine 1, Division of Nephrology, University Hospital Würzburg, Würzburg, Germany.

Turgay Saritas (T)

Department of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.

Martin Busch (M)

Department of Internal Medicine III, University Hospital Jena, Friedrich-Schiller Universität, Jena, Germany.

Ulla T Schultheiss (UT)

Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center and Department of Medicine IV - Nephrology and Primary Care, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.

Heike Meiselbach (H)

Department of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.

Nele Friedrich (N)

Institute of Clinical Chemistry and Laboratory Medicine, Greifswald, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, University Medicine, Greifswald, Germany.

Matthias Nauck (M)

Institute of Clinical Chemistry and Laboratory Medicine, Greifswald, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, University Medicine, Greifswald, Germany.

Jürgen Floege (J)

Department of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.

Florian Kronenberg (F)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Austria.

Christoph Wanner (C)

Department of Medicine 1, Division of Nephrology, University Hospital Würzburg, Würzburg, Germany.

Kai-Uwe Eckardt (KU)

Department of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, Germany.

Classifications MeSH