Associations between proteins and heavy metals in urine at low environmental exposures: Evidence of reverse causality

被引:85
作者
Chaumont, Agnes
Nickmilder, Marc
Dumont, Xavier
Lundh, Thomas [2 ]
Skerfving, Staffan [2 ]
Bernard, Alfred [1 ]
机构
[1] Catholic Univ Louvain, Fac Med, Lab Toxicol & Appl Pharmacol, Louvain Ctr Toxicol & Appl Pharmacol, B-1200 Brussels, Belgium
[2] Lund Univ, Div Occupat & Environm Med, Lund, Sweden
关键词
Cadmium; Lead; Heavy metals; Proteinuria; Albuminuria; Retinol-binding protein; beta(2)-microglobulin; Reverse causality; RETINOL-BINDING-PROTEIN; CADMIUM BODY BURDEN; RENAL UPTAKE; LOW-LEVEL; LATEX IMMUNOASSAY; METALLOTHIONEIN; POPULATION; EXCRETION; MEGALIN; BLOOD;
D O I
10.1016/j.toxlet.2012.02.005
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Heavy metals can cause renal effects on vulnerable populations but it is uncertain whether these metals still pose health risks at the low exposure levels now prevailing in most industrialized countries. In a cross-sectional study performed on 736 adolescents, we assessed the associations between the concentrations of cadmium and lead in blood and urine and the urinary concentrations of albumin and of low-molecular-weight (LMW) proteins, retinol-binding protein (RBP) and beta(2)-microglobulin. Multiple regression analyses were tested using urinary markers normalized to urinary creatinine or specific gravity. Median metal concentrations were in blood (mu g/L): lead. 15.1, cadmium, 0.18 and in urine (mu g/g creatinine): cadmium, 0.09 and lead, 0.82. Multivariate analyses revealed significant associations in urine between RBP and cadmium as well as between beta(2)-microglobulin and lead whereas no associations were seen with metals in blood. These associations were completely abolished in subjects with increased urinary albumin, which may be explained by the competitive inhibition of LMW protein reabsorption by albumin. Given the evidence that cadmium and lead circulate mainly bound to LMW proteins, these associations observed at low exposure might simply reflect the interindividual variations in the renal uptake of proteins sharing the same affinity for tubular binding sites. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:345 / 352
页数:8
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