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Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study
BACKGROUND: Tipepidine (3-[di-2-thienylmethylene]-1-methylpiperidine) has been used solely as a nonnarcotic antitussive in Japan since 1959. The safety of tipepidine in children and adults has already been established. It is reported that tipepidine inhibits G-protein-coupled inwardly rectifying pot...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908907/ https://www.ncbi.nlm.nih.gov/pubmed/24493927 http://dx.doi.org/10.2147/NDT.S58480 |
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author | Sasaki, Tsuyoshi Hashimoto, Kenji Tachibana, Masumi Kurata, Tsutomu Okawada, Keiko Ishikawa, Maki Kimura, Hiroshi Komatsu, Hideki Ishikawa, Masatomo Hasegawa, Tadashi Shiina, Akihiro Hashimoto, Tasuku Kanahara, Nobuhisa Shiraishi, Tetsuya Iyo, Masaomi |
author_facet | Sasaki, Tsuyoshi Hashimoto, Kenji Tachibana, Masumi Kurata, Tsutomu Okawada, Keiko Ishikawa, Maki Kimura, Hiroshi Komatsu, Hideki Ishikawa, Masatomo Hasegawa, Tadashi Shiina, Akihiro Hashimoto, Tasuku Kanahara, Nobuhisa Shiraishi, Tetsuya Iyo, Masaomi |
author_sort | Sasaki, Tsuyoshi |
collection | PubMed |
description | BACKGROUND: Tipepidine (3-[di-2-thienylmethylene]-1-methylpiperidine) has been used solely as a nonnarcotic antitussive in Japan since 1959. The safety of tipepidine in children and adults has already been established. It is reported that tipepidine inhibits G-protein-coupled inwardly rectifying potassium (GIRK)-channel currents. The inhibition of GIRK channels by tipepidine is expected to modulate the level of monoamines in the brain. We put forward the hypothesis that tipepidine can improve attention deficit/hyperactivity disorder (ADHD) symptoms by modulating monoaminergic neurotransmission through the inhibition of GIRK channels. The purpose of this open-label trial was to confirm whether treatment with tipepidine can improve symptoms in pediatric patients with ADHD. SUBJECTS AND METHODS: This was a 4-week, open-label, proof-of-efficacy pilot study for pediatric subjects with ADHD. Ten pediatric ADHD subjects (70% male; mean age, 9.9 years; combined [inattentive and hyperactive/impulsive] subtype, n=7; inattentive subtype, n=3; hyperimpulsive subtype, n=0) received tipepidine hibenzate taken orally at 30 mg/day for 4 weeks. All subjects were assessed using the ADHD Rating Scale IV (ADHD-RS), Japanese version, and the Das–Naglieri Cognitive Assessment System (DN-CAS), Japanese version. RESULTS: A comparison of baseline scores and 4-week end-point scores showed that all the ADHD-RS scores (total scores, hyperimpulsive subscores, and inattentive subscores) improved significantly (P<0.001). Furthermore, a comparison of baseline DN-CAS total scores and 4-week end-point scores showed a mild trend of improvement (P=0.093). Tipepidine was well tolerated, with no patients discontinuing medication because of side effects. CONCLUSION: Our pilot study suggests that tipepidine therapy may prove to be an effective alternative treatment for pediatric patients with ADHD. Nonetheless, more detailed randomized, double-blind trials are needed to confirm tipepidine’s efficacy. |
format | Online Article Text |
id | pubmed-3908907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39089072014-02-03 Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study Sasaki, Tsuyoshi Hashimoto, Kenji Tachibana, Masumi Kurata, Tsutomu Okawada, Keiko Ishikawa, Maki Kimura, Hiroshi Komatsu, Hideki Ishikawa, Masatomo Hasegawa, Tadashi Shiina, Akihiro Hashimoto, Tasuku Kanahara, Nobuhisa Shiraishi, Tetsuya Iyo, Masaomi Neuropsychiatr Dis Treat Original Research BACKGROUND: Tipepidine (3-[di-2-thienylmethylene]-1-methylpiperidine) has been used solely as a nonnarcotic antitussive in Japan since 1959. The safety of tipepidine in children and adults has already been established. It is reported that tipepidine inhibits G-protein-coupled inwardly rectifying potassium (GIRK)-channel currents. The inhibition of GIRK channels by tipepidine is expected to modulate the level of monoamines in the brain. We put forward the hypothesis that tipepidine can improve attention deficit/hyperactivity disorder (ADHD) symptoms by modulating monoaminergic neurotransmission through the inhibition of GIRK channels. The purpose of this open-label trial was to confirm whether treatment with tipepidine can improve symptoms in pediatric patients with ADHD. SUBJECTS AND METHODS: This was a 4-week, open-label, proof-of-efficacy pilot study for pediatric subjects with ADHD. Ten pediatric ADHD subjects (70% male; mean age, 9.9 years; combined [inattentive and hyperactive/impulsive] subtype, n=7; inattentive subtype, n=3; hyperimpulsive subtype, n=0) received tipepidine hibenzate taken orally at 30 mg/day for 4 weeks. All subjects were assessed using the ADHD Rating Scale IV (ADHD-RS), Japanese version, and the Das–Naglieri Cognitive Assessment System (DN-CAS), Japanese version. RESULTS: A comparison of baseline scores and 4-week end-point scores showed that all the ADHD-RS scores (total scores, hyperimpulsive subscores, and inattentive subscores) improved significantly (P<0.001). Furthermore, a comparison of baseline DN-CAS total scores and 4-week end-point scores showed a mild trend of improvement (P=0.093). Tipepidine was well tolerated, with no patients discontinuing medication because of side effects. CONCLUSION: Our pilot study suggests that tipepidine therapy may prove to be an effective alternative treatment for pediatric patients with ADHD. Nonetheless, more detailed randomized, double-blind trials are needed to confirm tipepidine’s efficacy. Dove Medical Press 2014-01-24 /pmc/articles/PMC3908907/ /pubmed/24493927 http://dx.doi.org/10.2147/NDT.S58480 Text en © 2014 Sasaki et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Sasaki, Tsuyoshi Hashimoto, Kenji Tachibana, Masumi Kurata, Tsutomu Okawada, Keiko Ishikawa, Maki Kimura, Hiroshi Komatsu, Hideki Ishikawa, Masatomo Hasegawa, Tadashi Shiina, Akihiro Hashimoto, Tasuku Kanahara, Nobuhisa Shiraishi, Tetsuya Iyo, Masaomi Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title | Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title_full | Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title_fullStr | Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title_full_unstemmed | Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title_short | Tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
title_sort | tipepidine in children with attention deficit/hyperactivity disorder: a 4-week, open-label, preliminary study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908907/ https://www.ncbi.nlm.nih.gov/pubmed/24493927 http://dx.doi.org/10.2147/NDT.S58480 |
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