Literature DB >> 3823521

[Biological aspects of occupational exposure to cadmium and several other metals].

R Lauwerys, J P Buchet, H Roels, A Bernard, J P Gennart.   

Abstract

We have performed several cross-sectional epidemiological surveys among workers exposed to cadmium, mercury vapour or manganese in order to assess : their early biological or functional effects; the biological tests allowing an assessment of the amount of metal absorbed or stored in the body; the acceptable exposure levels. Studies have also been carried out among persons exposed to inorganic arsenic in order to define its inactivation mechanism and to develop a biological test of exposure. The kidney is the main critical organ following long-term exposure to cadmium. To prevent the occurrence of renal changes in the majority of male workers exposed to cadmium, its concentration in renal cortex should not exceed 215 micrograms/g (wet weight), and that in urine : 10 micrograms/g creatinine. A blood cadmium level of 1 microgram/100 ml has been suggested as maximum tolerable level for long-term exposure. Prolonged exposure to mercury vapour may lead to renal and neurological disturbances. The preclinical signs of nephrotoxicity are correlated with the amount of mercury absorbed which may be assessed by monitoring the mercury level in urine. The neurotoxic effects (particularly tremor) are mainly related to the integrated exposure (duration and intensity). A maximal permissible level of 50 micrograms Hg/g urinary creatinine is proposed to prevent the occurrence of these toxic effects. An exposure to manganese dust for 7 years on the average at a level below the maximum allowable airborne concentration (5 mg/m3) recommended by the ACGIH in the USA may still lead to a slight reduction in psychomotor and spirometric performances and interfere with calcium metabolism.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3823521

Source DB:  PubMed          Journal:  Rev Epidemiol Sante Publique        ISSN: 0398-7620            Impact factor:   1.019


  4 in total

1.  Prenatal cadmium exposure alters postnatal immune cell development and function.

Authors:  Miranda L Hanson; Ida Holásková; Meenal Elliott; Kathleen M Brundage; Rosana Schafer; John B Barnett
Journal:  Toxicol Appl Pharmacol       Date:  2012-04-11       Impact factor: 4.219

2.  Prenatal cadmium exposure dysregulates sonic hedgehog and Wnt/beta-catenin signaling in the thymus resulting in altered thymocyte development.

Authors:  Miranda L Hanson; Kathleen M Brundage; Rosana Schafer; Janet C Tou; John B Barnett
Journal:  Toxicol Appl Pharmacol       Date:  2009-10-08       Impact factor: 4.219

3.  Prenatal cadmium exposure produces persistent changes to thymus and spleen cell phenotypic repertoire as well as the acquired immune response.

Authors:  Ida Holásková; Meenal Elliott; Miranda L Hanson; Rosana Schafer; John B Barnett
Journal:  Toxicol Appl Pharmacol       Date:  2012-10-23       Impact factor: 4.219

4.  Association between serum phosphorus and mortality in NHANES 2003-2006: the effect of gender and renal function.

Authors:  Luís Mendonça; Francisco Gonçalves; Susana Sampaio; Paulo Castro-Chaves; Luciano Pereira
Journal:  J Nephrol       Date:  2021-02-13       Impact factor: 3.902

  4 in total

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