Sclerostin is an independent risk factor for all-cause mortality in kidney transplant recipients

  • PDF / 1,243,419 Bytes
  • 7 Pages / 595.276 x 790.866 pts Page_size
  • 35 Downloads / 188 Views

DOWNLOAD

REPORT


ORIGINAL ARTICLE

Sclerostin is an independent risk factor for all‑cause mortality in kidney transplant recipients Shufei Zeng1,2 · Torsten Slowinski1 · Wolfgang Pommer3 · Ahmed A. Hasan2,4 · Mohamed M. S. Gaballa2,4,5 · Yongping Lu2,6 · Bernhard K. Krämer2 · Berthold Hocher2,7,8,9  Received: 11 February 2020 / Accepted: 7 August 2020 © The Author(s) 2020

Abstract Background  Sclerostin is a hormone contributing to the bone-vascular wall cross talk and has been implicated in cardiovascular events and mortality in patients with chronic kidney disease (CKD). We analyzed the relationship between sclerostin and mortality in renal transplant recipients. Methods  600 stable renal transplant recipients (367men, 233 women) were followed for all-cause mortality for 3 years. Blood and urine samples for analysis and clinical data were collected at study entry. We performed Kaplan–Meier survival analysis and Cox regression models considering confounding factors such as age, eGFR, cold ischemia time, HbA1c, phosphate, calcium, and albumin. Optimal cut-off values for the Cox regression model were calculated based on ROC analysis. Results  Sixty-five patients died during the observation period. Nonsurvivors (n = 65; sclerostin 57.31 ± 30.28 pmol/L) had higher plasma sclerostin levels than survivors (n = 535; sclerostin 47.52 ± 24.87 pmol/L) (p = 0.0036). Kaplan–Meier curve showed that baseline plasma sclerostin concentrations were associated with all-cause mortality in stable kidney transplant recipients (p = 0.0085, log-rank test). After multiple Cox regression analysis, plasma levels of sclerostin remained an independent predictor of all-cause mortality (hazard ratio, 1.011; 95% CI 1.002–1.020; p = 0.0137). Conclusions  Baseline plasma sclerostin is an independent risk factor for all-cause mortality in patients after kidney transplantation. Keywords  Kidney transplantation · All-cause mortality · Sclerostin

Introduction

Electronic supplementary material  The online version of this article (https​://doi.org/10.1007/s1015​7-020-01956​-y) contains supplementary material, which is available to authorized users. * Berthold Hocher [email protected]‑heidelberg.de 1



Department of Nephrology, Charité-Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany



Fifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany

2

3



4



KfH Kuratorium für Dialyse und Nierentransplantation e.V., Bildungszentrum, Neu‑Isenburg, Germany Institute of Nutritional Science, University of Potsdam, Potsdam, Germany

Kidney transplant  recipients  are a subset of patients with chronic kidney disease (CKD). And kidney transplantation is the treatment of choice for end-stage renal disease [1].

5



Faculty of Veterinary Medicine, Benha University, Moshtohor, Toukh, Egypt

6



Department of Nephrology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou, China

7



Institute of Medical Diagnostics, IMD Berlin, Ber