Literature DB >> 2565539

Chronic renal tubular effects in relation to urine cadmium levels.

P W Mueller1, S J Smith, K K Steinberg, M J Thun.   

Abstract

In this study the urine activities of two brush border membrane enzymes, alanine aminopeptidase (AAP) and gamma-glutamyltranspeptidase (GGT), and the lysosomal enzyme N-acetyl-beta-D-glucosaminidase (NAG) were measured in men exposed to cadmium to investigate chronic renal toxicity. The subjects consist of a group with urine cadmium levels less than 2.0 micrograms/l and a group with higher cadmium levels (urine cadmium greater than or equal to 2.0 micrograms/l) with past or present occupational exposure to cadmium. The mean NAG value corrected for creatinine in the higher cadmium group (2.95 U/g creatinine) is significantly different from the mean low cadmium group value (0.92 U/g creatinine, p = 0.0083). Likewise, AAP in the higher group (13.83 U/g creatinine) is significantly different from that of the low group (6.58 U/g creatinine; p = 0.0018). NAG and AAP also give significant correlations with cadmium levels in urine (NAG: r = 0.51; p = 0.0001; AAP: r = 0.56; p = 0.0001). There is no similar statistically significant difference in GGT means in the two groups. In contrast to cadmium correlations, blood lead does not correlate with NAG, AAP, or GGT. A dose-response relationship was found between NAG and cadmium and between AAP and cadmium. The analysis of this relationship gives estimates of a 10% chance of observing an elevated NAG value at a cadmium level of 6.3 micrograms/g creatinine (8.0 micrograms/l) and a 10% chance of observing an elevated AAP at a cadmium level of 5.0 micrograms/g creatinine (3.4 micrograms/l). These data indicate elevations of NAG and AAP at urine cadmium levels below the level of 10 micrograms/g creatinine recommended as an upper limit by the 1980 World Health Organization Study Group. Since elevated levels of NAG and AAP in cadmium-exposed workers may reflect chronic renal tubular nephrotoxicity, these findings indicate that cadmium levels below 10 micrograms/g creatinine may be accompanied by subclinical tubular dysfunction, and that WHO guidelines should be interpreted cautiously, particularly with reference to workers who are no longer exposed and may have had higher cadmium body burdens in the past.

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Year:  1989        PMID: 2565539     DOI: 10.1159/000185581

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  11 in total

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2.  Chronic renal effects in three studies of men and women occupationally exposed to cadmium.

Authors:  P W Mueller; D C Paschal; R R Hammel; S L Klincewicz; M L MacNeil; B Spierto; K K Steinberg
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3.  Biochemical response to cadmium. Dose-time effect.

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4.  Markers of early renal changes induced by industrial pollutants. III. Application to workers exposed to cadmium.

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Journal:  Br J Ind Med       Date:  1993-01

5.  A nine year follow up study of renal effects in workers exposed to cadmium in a zinc ore refinery.

Authors:  N J van Sittert; P H Ribbens; B Huisman; D Lugtenburg
Journal:  Br J Ind Med       Date:  1993-07

6.  Association between NAG-B and cadmium in urine with no evidence of a threshold.

Authors:  A Bernard; N Thielemans; H Roels; R Lauwerys
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7.  Effects of exposure to low levels of environmental cadmium on renal biomarkers.

Authors:  Curtis W Noonan; Sara M Sarasua; Dave Campagna; Steven J Kathman; Jeffrey A Lybarger; Patricia W Mueller
Journal:  Environ Health Perspect       Date:  2002-02       Impact factor: 9.031

8.  Cadmium burden and the risk and phenotype of prostate cancer.

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9.  Renal effects of environmental and occupational lead exposure.

Authors:  S K Rastogi
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Review 10.  New approaches for detecting thresholds of human nephrotoxicity using cadmium as an example.

Authors:  P W Mueller; R G Price; W F Finn
Journal:  Environ Health Perspect       Date:  1998-05       Impact factor: 9.031

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