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Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD

Objectives: Methylphenidate (MPH) is highly effective in controlling the symptoms of attention-deficit/hyperactivity disorder (ADHD), but some children with ADHD either do not respond to, or do not tolerate, treatment. Dextromethorphan (DM) is a neuroprotective agent which has been used in the treat...

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Autores principales: Chuang, Wei-Chen, Yeh, Chin-Bin, Wang, Sheng-Chiang, Pan, Pei-Yin, Shyu, Jia-Fwu, Liu, Yia-Ping, Gau, Susan Shur-Fen, Lu, Ru-Band
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620613/
https://www.ncbi.nlm.nih.gov/pubmed/31333511
http://dx.doi.org/10.3389/fpsyt.2019.00437
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author Chuang, Wei-Chen
Yeh, Chin-Bin
Wang, Sheng-Chiang
Pan, Pei-Yin
Shyu, Jia-Fwu
Liu, Yia-Ping
Gau, Susan Shur-Fen
Lu, Ru-Band
author_facet Chuang, Wei-Chen
Yeh, Chin-Bin
Wang, Sheng-Chiang
Pan, Pei-Yin
Shyu, Jia-Fwu
Liu, Yia-Ping
Gau, Susan Shur-Fen
Lu, Ru-Band
author_sort Chuang, Wei-Chen
collection PubMed
description Objectives: Methylphenidate (MPH) is highly effective in controlling the symptoms of attention-deficit/hyperactivity disorder (ADHD), but some children with ADHD either do not respond to, or do not tolerate, treatment. Dextromethorphan (DM) is a neuroprotective agent which has been used in the treatment of neuropsychiatric disorders. This clinical trial had examined the effect of DM on the use of MPH in the children with ADHD. Methods: This randomized double-blind clinical trial had evaluated 44 male outpatients, aged between 6 and 12 years, with a diagnosis of ADHD. The study subjects were randomly assigned into one of the two groups: receiving MPH alone (15–60 mg per day) or MPH plus DM (30–60 mg per day) for 8 weeks. Assessments, comprising the Chinese version of the Child Behavior Checklist (CBCL-C) scale and the Swanson, Nolan and Pelham Questionnaire (SNAP)-IV rating tests conducted by parents and the serum cytokines measured by microarray and enzyme-linked immunosorband assay (ELISA), were compared between groups at baseline and at 8 weeks after the medication was started. Results: There were a significant decrease at the mean scores of both CBCL-C and SNAP-IV scales after 8 weeks of treatment, but no significant differences between MPH and MPH+DM groups. Compared with the MPH-only group, the mean scores of some psychometric parameters reported on the CBCL-C and SNAP-IV scales regarding time effects as well as the attention problems on the CBCL-C scale regarding group effect were significantly higher in the DM+MPH group. Although there were no significant differences in the levels of various serum cytokines between groups, the subjects in the DM-MPH group had relatively fewer and lower levels of adverse effects. Significant interactions were found between the withdrawn/depression item reported on the CBCL-C scale and tumor necrosis factor α (ခTNF-α) (p = 0.027), as well as between thought problems item on the CBCL-C and TNF-α (p = 0.028) in subjects who had received DM+MPH treatment. Conclusion: Following the trial, DM+MPH was not superior to MPH alone for the treatment of children with ADHD, yet DM may potentially have negative effects on ADHD symptoms when combined with MPH. Clinical Trial Registration: Clinicaltrials.gov, trial number: NCT01787136.
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spelling pubmed-66206132019-07-22 Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD Chuang, Wei-Chen Yeh, Chin-Bin Wang, Sheng-Chiang Pan, Pei-Yin Shyu, Jia-Fwu Liu, Yia-Ping Gau, Susan Shur-Fen Lu, Ru-Band Front Psychiatry Psychiatry Objectives: Methylphenidate (MPH) is highly effective in controlling the symptoms of attention-deficit/hyperactivity disorder (ADHD), but some children with ADHD either do not respond to, or do not tolerate, treatment. Dextromethorphan (DM) is a neuroprotective agent which has been used in the treatment of neuropsychiatric disorders. This clinical trial had examined the effect of DM on the use of MPH in the children with ADHD. Methods: This randomized double-blind clinical trial had evaluated 44 male outpatients, aged between 6 and 12 years, with a diagnosis of ADHD. The study subjects were randomly assigned into one of the two groups: receiving MPH alone (15–60 mg per day) or MPH plus DM (30–60 mg per day) for 8 weeks. Assessments, comprising the Chinese version of the Child Behavior Checklist (CBCL-C) scale and the Swanson, Nolan and Pelham Questionnaire (SNAP)-IV rating tests conducted by parents and the serum cytokines measured by microarray and enzyme-linked immunosorband assay (ELISA), were compared between groups at baseline and at 8 weeks after the medication was started. Results: There were a significant decrease at the mean scores of both CBCL-C and SNAP-IV scales after 8 weeks of treatment, but no significant differences between MPH and MPH+DM groups. Compared with the MPH-only group, the mean scores of some psychometric parameters reported on the CBCL-C and SNAP-IV scales regarding time effects as well as the attention problems on the CBCL-C scale regarding group effect were significantly higher in the DM+MPH group. Although there were no significant differences in the levels of various serum cytokines between groups, the subjects in the DM-MPH group had relatively fewer and lower levels of adverse effects. Significant interactions were found between the withdrawn/depression item reported on the CBCL-C scale and tumor necrosis factor α (ခTNF-α) (p = 0.027), as well as between thought problems item on the CBCL-C and TNF-α (p = 0.028) in subjects who had received DM+MPH treatment. Conclusion: Following the trial, DM+MPH was not superior to MPH alone for the treatment of children with ADHD, yet DM may potentially have negative effects on ADHD symptoms when combined with MPH. Clinical Trial Registration: Clinicaltrials.gov, trial number: NCT01787136. Frontiers Media S.A. 2019-06-26 /pmc/articles/PMC6620613/ /pubmed/31333511 http://dx.doi.org/10.3389/fpsyt.2019.00437 Text en Copyright © 2019 Chuang, Yeh, Wang, Pan, Shyu, Liu, Gau and Lu http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Chuang, Wei-Chen
Yeh, Chin-Bin
Wang, Sheng-Chiang
Pan, Pei-Yin
Shyu, Jia-Fwu
Liu, Yia-Ping
Gau, Susan Shur-Fen
Lu, Ru-Band
Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title_full Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title_fullStr Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title_full_unstemmed Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title_short Potential Negative Effects of Dextromethorphan as an Add-On Therapy to Methylphenidate in Children With ADHD
title_sort potential negative effects of dextromethorphan as an add-on therapy to methylphenidate in children with adhd
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620613/
https://www.ncbi.nlm.nih.gov/pubmed/31333511
http://dx.doi.org/10.3389/fpsyt.2019.00437
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