Abstract

BackgroundUrinary kidney injury molecule 1 is a recently discovered early biomarker for renal damage that has been proven to be correlated to urinary cadmium in rats. However, so far the association between urinary cadmium and kidney injury molecule 1 in humans after long-term, low-dose cadmium exposure has not been studied.MethodsWe collected urine and blood samples from 153 non-smoking men and women aged 60+, living in an area with moderate cadmium pollution from a non-ferrous metal plant for a significant period. Urinary cadmium and urinary kidney injury molecule 1 as well as other renal biomarkers (alpha1-microglobulin, beta2-microglobulin, blood urea nitrogen, urinary proteins and microalbumin) were assessed.ResultsBoth before (r = 0.20; p = 0.01) and after (partial r = 0.32; p < 0.0001) adjustment for creatinine, age, sex, past smoking, socio-economic status and body mass index, urinary kidney injury molecule 1 correlated with urinary cadmium concentrations. No significant association was found between the other studied renal biomarkers and urinary cadmium.ConclusionsWe showed that urinary kidney injury molecule 1 levels are positively correlated with urinary cadmium concentration in an elderly population after long-term, low-dose exposure to cadmium, while other classical markers do not show an association. Therefore, urinary kidney injury molecule 1 might be considered as a biomarker for early-stage metal-induced kidney injury by cadmium.

Highlights

  • Urinary kidney injury molecule 1 is a recently discovered early biomarker for renal damage that has been proven to be correlated to urinary cadmium in rats

  • Kidney injury molecule 1 (KIM-1), originally discovered by Ichimura et al, is a type 1 membrane glycoprotein found on renal proximal tubule epithelial cells

  • Informed consent was obtained from all participants and the study was approved by the ethics committee of the Ziekenhuis Oost-Limburg (ZOL), Belgium

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Summary

Introduction

Urinary kidney injury molecule 1 is a recently discovered early biomarker for renal damage that has been proven to be correlated to urinary cadmium in rats. To the bone [3], a main target for chronic, low-level Cd exposure is the kidney, leading to early and stable biomarker for proximal tubule damage caused by Cd. Kidney injury molecule 1 (KIM-1), originally discovered by Ichimura et al, is a type 1 membrane glycoprotein found on renal proximal tubule epithelial cells. Kidney injury molecule 1 (KIM-1), originally discovered by Ichimura et al, is a type 1 membrane glycoprotein found on renal proximal tubule epithelial cells It contains in its extracellular portion a unique 6-cysteine immunoglobulin-like domain and a mucin-domain [18]. An intracellular highly conserved tyrosine kinase phosphorylation motif is a strong indicator that KIM-1 is a cell signaling molecule [19]

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