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Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results

BACKGROUND: This study investigated the effects of oral dimercapto succinic acid (DMSA) therapy on the behavioural symptoms of children with autism spectrum disorders (ASD) ages 3-8 years. METHODS: Phase 1 involved 65 children with ASD who received one round of DMSA (3 days). Participants who had hi...

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Autores principales: Adams, James B, Baral, Matthew, Geis, Elizabeth, Mitchell, Jessica, Ingram, Julie, Hensley, Andrea, Zappia, Irene, Newmark, Sanford, Gehn, Eva, Rubin, Robert A, Mitchell, Ken, Bradstreet, Jeff, El-Dahr, Jane
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770991/
https://www.ncbi.nlm.nih.gov/pubmed/19852790
http://dx.doi.org/10.1186/1472-6904-9-17
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author Adams, James B
Baral, Matthew
Geis, Elizabeth
Mitchell, Jessica
Ingram, Julie
Hensley, Andrea
Zappia, Irene
Newmark, Sanford
Gehn, Eva
Rubin, Robert A
Mitchell, Ken
Bradstreet, Jeff
El-Dahr, Jane
author_facet Adams, James B
Baral, Matthew
Geis, Elizabeth
Mitchell, Jessica
Ingram, Julie
Hensley, Andrea
Zappia, Irene
Newmark, Sanford
Gehn, Eva
Rubin, Robert A
Mitchell, Ken
Bradstreet, Jeff
El-Dahr, Jane
author_sort Adams, James B
collection PubMed
description BACKGROUND: This study investigated the effects of oral dimercapto succinic acid (DMSA) therapy on the behavioural symptoms of children with autism spectrum disorders (ASD) ages 3-8 years. METHODS: Phase 1 involved 65 children with ASD who received one round of DMSA (3 days). Participants who had high urinary excretion of toxic metals were selected to continue on to phase 2. In phase 2, 49 participants were randomly assigned in a double-blind design to receive an additional 6 rounds of either DMSA or placebo. RESULTS: The groups receiving one round and seven rounds of DMSA had significant improvements on all the assessment measures. For the seven round group, the degree of improvement on the assessment measures could be partially explained by a regression analysis based on excretion of toxic metals and changes in glutathione (adjusted R(2 )of 0.28-0.75, p < 0.02 in all cases). One round of DMSA had nearly the same benefit as seven rounds. The assessment measures correlated reasonably with one another at the beginning of the study (r = 0.60-0.87) and even better at the end of the study (r = 0.63-0.94). CONCLUSION: Overall, both one and seven rounds of DMSA therapy seems to be reasonably safe in children with ASD who have high urinary excretion of toxic metals, and possibly helpful in reducing some of the symptoms of autism in those children.
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spelling pubmed-27709912009-10-31 Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results Adams, James B Baral, Matthew Geis, Elizabeth Mitchell, Jessica Ingram, Julie Hensley, Andrea Zappia, Irene Newmark, Sanford Gehn, Eva Rubin, Robert A Mitchell, Ken Bradstreet, Jeff El-Dahr, Jane BMC Clin Pharmacol Research Article BACKGROUND: This study investigated the effects of oral dimercapto succinic acid (DMSA) therapy on the behavioural symptoms of children with autism spectrum disorders (ASD) ages 3-8 years. METHODS: Phase 1 involved 65 children with ASD who received one round of DMSA (3 days). Participants who had high urinary excretion of toxic metals were selected to continue on to phase 2. In phase 2, 49 participants were randomly assigned in a double-blind design to receive an additional 6 rounds of either DMSA or placebo. RESULTS: The groups receiving one round and seven rounds of DMSA had significant improvements on all the assessment measures. For the seven round group, the degree of improvement on the assessment measures could be partially explained by a regression analysis based on excretion of toxic metals and changes in glutathione (adjusted R(2 )of 0.28-0.75, p < 0.02 in all cases). One round of DMSA had nearly the same benefit as seven rounds. The assessment measures correlated reasonably with one another at the beginning of the study (r = 0.60-0.87) and even better at the end of the study (r = 0.63-0.94). CONCLUSION: Overall, both one and seven rounds of DMSA therapy seems to be reasonably safe in children with ASD who have high urinary excretion of toxic metals, and possibly helpful in reducing some of the symptoms of autism in those children. BioMed Central 2009-10-23 /pmc/articles/PMC2770991/ /pubmed/19852790 http://dx.doi.org/10.1186/1472-6904-9-17 Text en Copyright © 2009 Adams et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Adams, James B
Baral, Matthew
Geis, Elizabeth
Mitchell, Jessica
Ingram, Julie
Hensley, Andrea
Zappia, Irene
Newmark, Sanford
Gehn, Eva
Rubin, Robert A
Mitchell, Ken
Bradstreet, Jeff
El-Dahr, Jane
Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title_full Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title_fullStr Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title_full_unstemmed Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title_short Safety and efficacy of oral DMSA therapy for children with autism spectrum disorders: Part B - Behavioral results
title_sort safety and efficacy of oral dmsa therapy for children with autism spectrum disorders: part b - behavioral results
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770991/
https://www.ncbi.nlm.nih.gov/pubmed/19852790
http://dx.doi.org/10.1186/1472-6904-9-17
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