The physiological determinants of low-level urine cadmium: an assessment in a cross-sectional study among schoolchildren

被引:14
作者
Wang, Hongyu [1 ]
Dumont, Xavier [1 ]
Haufroid, Vincent [1 ]
Bernard, Alfred [1 ]
机构
[1] Catholic Univ Louvain, IREC, Louvain Ctr Toxicol & Appl Pharmacol, Ave Emmanuel Mounier 53-02, B-1200 Brussels, Belgium
关键词
Cadmium; Biomarker; Club cell protein; alfa(1)-microglobulin; Protein HC; Retinol-binding protein; beta(2)-microglobulin; ENVIRONMENTAL EXPOSURE; LATEX IMMUNOASSAY; KIDNEY-FUNCTION; ZINC LEVELS; POPULATION; ASSOCIATIONS; CREATININE; EXCRETION; PROTEINS; CHILDREN;
D O I
10.1186/s12940-017-0306-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Recent studies in children have reported associations of urinary cadmium (U-Cd), used as biomarker of Cd body burden, with renal dysfunction, retarded growth and impaired cognitive development in children. Little is known, however, about factors influencing U-Cd in children and likely to act as confounders. Methods: In a cross-sectional study involving 249 schoolchildren (mean age, 5.72 years; 138 boys), we measured the urine concentrations of cadmium, zinc, lead, albumin, alpha(1)-microglobulin (A1M), retinol-binding protein, beta(2)-microglobulin and club cell protein (CC16). Determinants of U-Cd expressed per creatinine or adjusted to specific gravity were identified by multiple regression analyses. Results: Girls and boys had similar median concentrations of U-Cd (0.22 and 0.24 mu g/L, 0.33 and 0.35 mu g/g creatinine, respectively). When models were run without including creatinine or specific gravity among independent variables, urinary zinc, urinary A1M and age emerged as the strongest predictors of U-Cd expressed per g creatinine or adjusted to SG. When adding creatinine among predictors, urinary creatinine emerged as an additional strong predictor correlating negatively with U-Cd per g creatinine. This strong residual influence of diuresis, not seen when adding specific gravity among predictors, linked U-Cd to U-A1M or U-CC16 through secondary associations mimicking those induced by Cd nephrotoxity. Conclusions: In young children U-Cd largely varies with diuresis, zinc metabolism and urinary A1M. These physiological determinants, unrelated to Cd body burden, may confound the child renal and developmental outcomes associated with low-level U-Cd.
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页数:12
相关论文
共 42 条
[1]   Variability of urinary cadmium excretion in spot urine samples, first morning voids, and 24 h urine in a healthy non-smoking population: Implications for study design [J].
Akerstrom, Magnus ;
Barregard, Lars ;
Lundh, Thomas ;
Sallsten, Gerd .
JOURNAL OF EXPOSURE SCIENCE AND ENVIRONMENTAL EPIDEMIOLOGY, 2014, 24 (02) :171-179
[2]   Associations between Urinary Excretion of Cadmium and Proteins in a Nonsmoking Population: Renal Toxicity or Normal Physiology? [J].
Akerstrom, Magnus ;
Sallsten, Gerd ;
Lundh, Thomas ;
Barregard, Lars .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2013, 121 (02) :187-191
[3]   Urinary creatinine concentrations in the US population: Implications for urinary biologic monitoring measurements [J].
Barr, DB ;
Wilder, LC ;
Caudill, SP ;
Gonzalez, AJ ;
Needham, LL ;
Pirkle, JL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (02) :192-200
[4]   Renal dysfunction induced by cadmium: biomarkers of critical effects [J].
Bernard, A .
BIOMETALS, 2004, 17 (05) :519-523
[5]   Biomarkers of metal toxicity in population studies: Research potential and interpretation issues [J].
Bernard, Alfred .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2008, 71 (18) :1259-1265
[6]   Confusion about Cadmium Risks: The Unrecognized Limitations of an Extrapolated Paradigm [J].
Bernard, Alfred .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2016, 124 (01) :1-5
[7]  
BERNARD AM, 1981, CLIN CHEM, V27, P832
[8]   THE EFFECTS OF LOW-DOSES OF CADMIUM METALLOTHIONEIN ON THE RENAL UPTAKE OF BETA-2-MICROGLOBULIN IN RATS [J].
BERNARD, AM ;
AMOR, AO ;
LAUWERYS, RR .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1987, 87 (03) :440-445
[9]  
BERNARD AM, 1983, CLIN CHEM, V29, P1007
[10]  
BERNARD AM, 1982, CLIN CHEM, V28, P1167