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Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial

BACKGROUND: Mercury is nephrotoxic and dental amalgam is a source of mercury exposure. METHODS: Children 6–10 years of age (n = 534) with two or more posterior teeth with caries but no prior amalgam restorations, were randomized to one of two treatments—amalgam or resin composite (white fillings)—us...

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Autores principales: Barregard, Lars, Trachtenberg, Felicia, McKinlay, Sonja
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265055/
https://www.ncbi.nlm.nih.gov/pubmed/18335109
http://dx.doi.org/10.1289/ehp.10504
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author Barregard, Lars
Trachtenberg, Felicia
McKinlay, Sonja
author_facet Barregard, Lars
Trachtenberg, Felicia
McKinlay, Sonja
author_sort Barregard, Lars
collection PubMed
description BACKGROUND: Mercury is nephrotoxic and dental amalgam is a source of mercury exposure. METHODS: Children 6–10 years of age (n = 534) with two or more posterior teeth with caries but no prior amalgam restorations, were randomized to one of two treatments—amalgam or resin composite (white fillings)—used for caries treatment during 5 years of follow-up. The primary outcome was change in IQ, but important secondary outcomes were effects on markers of glomerular and tubular kidney function: urinary excretion of albumin, alpha-1-microglobulin (A1M), γ-glutamyl transpeptidase (γ-GT), and N-acetyl-β-d-glucosaminidase (NAG). These markers were measured on several occasions during the trial, together with urinary mercury and covariates. We evaluated the results using repeated-measures analyses. RESULTS: There were no significant differences between treatment groups in average levels of renal biomarkers, nor significant effects of number of dental amalgams on these markers. There was, however, a significantly increased prevalence of microalbuminuria (MA) among children in the amalgam group in years 3–5 (adjusted odds ratio 1.8; 95% confidence interval, 1.1–2.9). Most of these cases are likely to be temporary MA, but 10 children in the amalgam group had MA in both years 3 and 5, versus 2 children in the composite group (p = 0.04). There were no differences in the occurrence of high levels of renal tubular markers (A1M, γ-GT, or NAG). CONCLUSIONS: The increase in MA may be a random finding, but should be tested further. The results did not support recent findings in an observational study of an effect of low-level mercury on tubular biomarkers in children.
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spelling pubmed-22650552008-03-11 Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial Barregard, Lars Trachtenberg, Felicia McKinlay, Sonja Environ Health Perspect Research BACKGROUND: Mercury is nephrotoxic and dental amalgam is a source of mercury exposure. METHODS: Children 6–10 years of age (n = 534) with two or more posterior teeth with caries but no prior amalgam restorations, were randomized to one of two treatments—amalgam or resin composite (white fillings)—used for caries treatment during 5 years of follow-up. The primary outcome was change in IQ, but important secondary outcomes were effects on markers of glomerular and tubular kidney function: urinary excretion of albumin, alpha-1-microglobulin (A1M), γ-glutamyl transpeptidase (γ-GT), and N-acetyl-β-d-glucosaminidase (NAG). These markers were measured on several occasions during the trial, together with urinary mercury and covariates. We evaluated the results using repeated-measures analyses. RESULTS: There were no significant differences between treatment groups in average levels of renal biomarkers, nor significant effects of number of dental amalgams on these markers. There was, however, a significantly increased prevalence of microalbuminuria (MA) among children in the amalgam group in years 3–5 (adjusted odds ratio 1.8; 95% confidence interval, 1.1–2.9). Most of these cases are likely to be temporary MA, but 10 children in the amalgam group had MA in both years 3 and 5, versus 2 children in the composite group (p = 0.04). There were no differences in the occurrence of high levels of renal tubular markers (A1M, γ-GT, or NAG). CONCLUSIONS: The increase in MA may be a random finding, but should be tested further. The results did not support recent findings in an observational study of an effect of low-level mercury on tubular biomarkers in children. National Institute of Environmental Health Sciences 2008-03 2007-11-23 /pmc/articles/PMC2265055/ /pubmed/18335109 http://dx.doi.org/10.1289/ehp.10504 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Barregard, Lars
Trachtenberg, Felicia
McKinlay, Sonja
Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title_full Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title_fullStr Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title_full_unstemmed Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title_short Renal Effects of Dental Amalgam in Children: The New England Children’s Amalgam Trial
title_sort renal effects of dental amalgam in children: the new england children’s amalgam trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265055/
https://www.ncbi.nlm.nih.gov/pubmed/18335109
http://dx.doi.org/10.1289/ehp.10504
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