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Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder

BACKGROUND: There is a critical need for effective treatment of the core symptoms of autism spectrum disorder (ASD). The purinergic antagonist suramin may improve core symptoms through restoration of normal mitochondrial function and reduction of neuro-inflammation via its known antagonism of P2X an...

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Autores principales: Hough, David, Mao, Alice R., Aman, Michael, Lozano, Reymundo, Smith-Hicks, Constance, Martinez-Cerdeno, Veronica, Derby, Michael, Rome, Zachary, Malan, Niel, Findling, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626700/
https://www.ncbi.nlm.nih.gov/pubmed/37932739
http://dx.doi.org/10.1186/s12991-023-00477-8
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author Hough, David
Mao, Alice R.
Aman, Michael
Lozano, Reymundo
Smith-Hicks, Constance
Martinez-Cerdeno, Veronica
Derby, Michael
Rome, Zachary
Malan, Niel
Findling, Robert L.
author_facet Hough, David
Mao, Alice R.
Aman, Michael
Lozano, Reymundo
Smith-Hicks, Constance
Martinez-Cerdeno, Veronica
Derby, Michael
Rome, Zachary
Malan, Niel
Findling, Robert L.
author_sort Hough, David
collection PubMed
description BACKGROUND: There is a critical need for effective treatment of the core symptoms of autism spectrum disorder (ASD). The purinergic antagonist suramin may improve core symptoms through restoration of normal mitochondrial function and reduction of neuro-inflammation via its known antagonism of P2X and P2Y receptors. Nonclinical studies in fragile X knockout mice and the maternal immune activation model support these hypotheses. METHODS: We conducted a 14 week, randomized, double-blind, placebo-controlled proof -of-concept study (N = 52) to test the efficacy and safety of suramin intravenous infusions in boys aged 4–15 years with moderate to severe ASD. The study had 3 treatment arms: 10 mg/kg suramin, 20 mg/kg suramin, and placebo given at baseline, week 4, and week 8. The Aberrant Behavior Checklist of Core Symptoms (ABC-Core) (subscales 2, 3, and 5) was the primary endpoint and the Clinical Global Impressions—Improvement (CGI-I) was a secondary endpoint. RESULTS: Forty-four subjects completed the study. The 10 mg/kg suramin group showed a greater, but statistically non-significant, numeric improvement (− 12.5 ± 3.18 [mean ± SE]) vs. placebo (− 8.9 ± 2.86) in ABC-Core at Week 14. The 20 mg/kg suramin group did not show improvement over placebo. In exploratory analyses, the 10 mg/kg arm showed greater ABC Core differences from placebo in younger subjects and among those with less severe symptoms. In CGI-I, the 10 mg/kg arm showed a statistically significant improvement from baseline (2.8 ± 0.30 [mean ± SE]) compared to placebo (1.7 ± 0.27) (p = 0.016). The 20 mg/kg arm had a 2.0 ± 0.28 improvement in CGI-I, which was not statistically significant compared to placebo (p = 0.65). CONCLUSION: Suramin was generally safe and well tolerated over 14 weeks; most adverse events were mild to moderate in severity. Trial Registration Registered with the South African Health Authority, registration number DOH-27–0419-6116. ClinicalTrials.Gov registration ID is NCT06058962, last update posted 2023–09-28.
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spelling pubmed-106267002023-11-07 Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder Hough, David Mao, Alice R. Aman, Michael Lozano, Reymundo Smith-Hicks, Constance Martinez-Cerdeno, Veronica Derby, Michael Rome, Zachary Malan, Niel Findling, Robert L. Ann Gen Psychiatry Research BACKGROUND: There is a critical need for effective treatment of the core symptoms of autism spectrum disorder (ASD). The purinergic antagonist suramin may improve core symptoms through restoration of normal mitochondrial function and reduction of neuro-inflammation via its known antagonism of P2X and P2Y receptors. Nonclinical studies in fragile X knockout mice and the maternal immune activation model support these hypotheses. METHODS: We conducted a 14 week, randomized, double-blind, placebo-controlled proof -of-concept study (N = 52) to test the efficacy and safety of suramin intravenous infusions in boys aged 4–15 years with moderate to severe ASD. The study had 3 treatment arms: 10 mg/kg suramin, 20 mg/kg suramin, and placebo given at baseline, week 4, and week 8. The Aberrant Behavior Checklist of Core Symptoms (ABC-Core) (subscales 2, 3, and 5) was the primary endpoint and the Clinical Global Impressions—Improvement (CGI-I) was a secondary endpoint. RESULTS: Forty-four subjects completed the study. The 10 mg/kg suramin group showed a greater, but statistically non-significant, numeric improvement (− 12.5 ± 3.18 [mean ± SE]) vs. placebo (− 8.9 ± 2.86) in ABC-Core at Week 14. The 20 mg/kg suramin group did not show improvement over placebo. In exploratory analyses, the 10 mg/kg arm showed greater ABC Core differences from placebo in younger subjects and among those with less severe symptoms. In CGI-I, the 10 mg/kg arm showed a statistically significant improvement from baseline (2.8 ± 0.30 [mean ± SE]) compared to placebo (1.7 ± 0.27) (p = 0.016). The 20 mg/kg arm had a 2.0 ± 0.28 improvement in CGI-I, which was not statistically significant compared to placebo (p = 0.65). CONCLUSION: Suramin was generally safe and well tolerated over 14 weeks; most adverse events were mild to moderate in severity. Trial Registration Registered with the South African Health Authority, registration number DOH-27–0419-6116. ClinicalTrials.Gov registration ID is NCT06058962, last update posted 2023–09-28. BioMed Central 2023-11-06 /pmc/articles/PMC10626700/ /pubmed/37932739 http://dx.doi.org/10.1186/s12991-023-00477-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hough, David
Mao, Alice R.
Aman, Michael
Lozano, Reymundo
Smith-Hicks, Constance
Martinez-Cerdeno, Veronica
Derby, Michael
Rome, Zachary
Malan, Niel
Findling, Robert L.
Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title_full Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title_fullStr Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title_full_unstemmed Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title_short Randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
title_sort randomized clinical trial of low dose suramin intravenous infusions for treatment of autism spectrum disorder
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626700/
https://www.ncbi.nlm.nih.gov/pubmed/37932739
http://dx.doi.org/10.1186/s12991-023-00477-8
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