Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort
Katharina Charlotte Reimer , Jennifer Nadal , Heike Meiselbach , Matthias Schmid , Ulla T. Schultheiss , Fruzsina Kotsis , Helena Stockmann , Nele Friedrich , Matthias Nauck , Vera Krane , Kai-Uwe Eckardt , Markus P. Schneider , Rafael Kramann , Jürgen Floege , Turgay Saritas , GCKD study investigators on behalf of the , Mario Schiffer , Hans-Ulrich Prokosch , Barbara Bärthlein , Andreas Beck , André Reis , Arif B. Ekici , Susanne Becker , Ulrike Alberth-Schmidt , Anke Weigel , Sabine Marschall , Eugenia Schefler , Gerd Walz , Anna Köttgen , Fruzsina Kotsis , Simone Meder , Erna Mitsch , Ursula Reinhard , Elke Schaeffner , Seema Baid-Agrawal , Kerstin Theisen , Kai Schmidt-Ott , Martin Zeier , Claudia Sommerer , Mehtap Aykac , Gunter Wolf , Rainer Paul , Antje Börner-Klein , Britta Bauer , Julia Raschenberger , Barbara Kollerits , Lukas Forer , Sebastian Schönherr , Hansi Weissensteiner , Peter Oefner , Wolfram Gronwald
Bone Research ›› 2023, Vol. 11 ›› Issue (1) : 52
Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort
Mineral and bone disorder (MBD) in chronic kidney disease (CKD) is tightly linked to cardiovascular disease (CVD). In this study, we aimed to compare the prognostic value of nine MBD biomarkers to determine those associated best with adverse cardiovascular (CV) outcomes and mortality. In 5 217 participants of the German CKD (GCKD) study enrolled with an estimated glomerular filtration rate (eGFR) between 30–60 mL·min−1 per 1.73 m2 or overt proteinuria, serum osteoprotegerin (OPG), C-terminal fibroblast growth factor-23 (FGF23), intact parathyroid hormone (iPTH), bone alkaline phosphatase (BAP), cross-linked C-telopeptide of type 1 collagen (CTX1), procollagen 1 intact N-terminal propeptide (P1NP), phosphate, calcium, and 25-OH vitamin D were measured at baseline. Participants with missing values among these parameters (n = 971) were excluded, leaving a total of 4 246 participants for analysis. During a median follow-up of 6.5 years, 387 non-CV deaths, 173 CV deaths, 645 nonfatal major adverse CV events (MACEs) and 368 hospitalizations for congestive heart failure (CHF) were observed. OPG and FGF23 were associated with all outcomes, with the highest hazard ratios (HRs) for OPG. In the final Cox regression model, adjusted for CV risk factors, including kidney function and all other investigated biomarkers, each standard deviation increase in OPG was associated with non-CV death (HR 1.76, 95% CI: 1.35–2.30), CV death (HR 2.18, 95% CI: 1.50–3.16), MACE (HR 1.38, 95% CI: 1.12–1.71) and hospitalization for CHF (HR 2.05, 95% CI: 1.56–2.69). Out of the nine biomarkers examined, stratification based on serum OPG best identified the CKD patients who were at the highest risk for any adverse CV outcome and mortality.
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Else Kröner-Fresenius-Stiftung (Else Kroner-Fresenius Foundation)(2022_EKES.03)
German Society of Internal Medicine 361357
Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research)(01ZX1912B)
KfH (Kuratorium für Heimdialyse und Nierentransplantation e.V.—Stiftung Präventivmedizin- no grant number
Deutsche Forschungsgemeinschaft (German Research Foundation)(322900939)
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