Urinary excretion of epidermal growth factor and rapid loss of kidney function

Author:

Norvik Jon Viljar12,Harskamp Laura R3,Nair Viji4,Shedden Kerby5,Solbu Marit D12,Eriksen Bjørn O12,Kretzler Matthias46,Gansevoort Ron T3,Ju Wenjun46,Melsom Toralf12

Affiliation:

1. Metabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway

2. Section of Nephrology, University Hospital of North Norway, Tromsø, Norway

3. Department of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

4. Department of Internal Medicine/Nephrology, University of Michigan, Ann Arbor, MI, USA

5. Department of Statistics, University of Michigan, Ann Arbor, MI, USA

6. Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA

Abstract

Abstract Background Lower urinary excretion of the kidney tubule–specific biomarker epidermal growth factor (uEGF) is associated with increased risk of renal function [glomerular filtration rate (GFR)] loss in diabetes and in patients with established chronic kidney disease (CKD). We investigated whether uEGF is associated with rapid GFR decline or incident CKD in the general population. Methods Subjects without CKD or diabetes were recruited from the general population in Tromso, Norway [Renal Iohexol Clearance Survey (RENIS); N = 1249] and Groningen, the Netherlands [Prevention of REnal and Vascular END-stage disease (PREVEND); N = 4534], with a median follow-up of 5.6 and 7.4 years, respectively. GFR was measured by iohexol clearance in the RENIS and estimated using the CKD Epidemiology Collaboration creatinine–cystatin C equation in the PREVEND study. Rapid GFR decline was defined as an annual GFR loss >3.0 mL/min/1.73 m2 and in sensitivity analyses as subjects with the 10% steepest GFR slope within each cohort. Results Lower baseline uEGF excretion was associated with rapid GFR loss in both cohorts {RENIS, odds ratio [OR] per 1 μg/mmol lower uEGF 1.42 [95% confidence interval (CI) 1.06–1.91], P = 0.02; PREVEND, OR 1.29 [95% CI 1.10–1.53], P < 0.01}, adjusted for baseline GFR, albumin:creatinine ratio and conventional CKD risk factors. Similar results were obtained using the outcome of the 10% steepest GFR slope in each cohort. Lower uEGF levels were associated with incident CKD in the combined analysis of both cohorts. Conclusions Lower uEGF levels are associated with increased risk of rapid GFR loss and incident CKD in the general population. This finding, together with previous findings in CKD and high-risk populations, supports that uEGF may serve as a broadly applicable biomarker representing the tubular component of the current glomerulus-centric clinical risk assessment system.

Funder

Northern Norway Regional Health Authority

UiT The Arctic University of Norway and by an unrestricted grant from Boehringer-Ingelheim

Dutch Kidney Foundation and the Dutch Heart Foundation

Dutch Government, the US National Institutes of Health and the University Medical Center Groningen, the Netherlands

Applied Systems Biology Core of the University of Michigan George M. O’Brien Kidney Research Core Center

NIH

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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