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| Research article summary (published 14 Jun 2006): |
Porphyrinuria in childhood autistic disorder: implications for environmental toxicity.
Full Abstract
To address a possible environmental contribution to autism, we carried out a retrospective study on urinary porphyrin levels, a biomarker of environmental toxicity, in 269 children with neurodevelopmental and related disorders referred to a Paris clinic (2002-2004), including 106 with autistic disorder. Urinary porphyrin levels determined by high-performance liquid chromatography were compared between diagnostic groups including internal and external control groups. Coproporphyrin levels were elevated in children with autistic disorder relative to control groups. Elevation was maintained on normalization for age or to a control heme pathway metabolite (uroporphyrin) in the same samples. The elevation was significant (P < 0.001). Porphyrin levels were unchanged in Asperger's disorder, distinguishing it from autistic disorder. The atypical molecule precoproporphyrin, a specific indicator of heavy metal toxicity, was also elevated in autistic disorder (P < 0.001) but not significantly in Asperger's. A subgroup with autistic disorder was treated with oral dimercaptosuccinic acid (DMSA) with a view to heavy metal removal. Following DMSA there was a significant (P = 0.002) drop in urinary porphyrin excretion. These data implicate environmental toxicity in childhood autistic disorder.
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Author information
Author/s: Nataf, Robert (R); Skorupka, Corinne (C); Amet, Lorene (L); Lam, Alain (A); Springbett, Anthea (A); Lathe, Richard (R);
Affiliation: Laboratoire Philippe Auguste, Paris, France.
Journal and publication information
Publication Type: Comparative Study; Journal Article
Journal: Toxicology and applied pharmacology (Toxicol Appl Pharmacol), published in United States. (Language: eng)
Reference: 2006-Jul; vol 214 (issue 2) : pp 99-108
Dates: Created 2006/07/17; Completed 2006/09/11; Revised 2006/11/15;
PMID: 16782144, status: MEDLINE (last retrieval date: 12/26/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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