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Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder
OBJECTIVE: The aims of the present study were to analyze the association between discontinuation of paroxetine (PAX) and the genetic variants of the polymorphism in the serotonin transporter gene-linked polymorphic region (5-HTTLPR) in Japanese patients with panic disorder (PD) and major depressive...
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/PMC4174019/ https://www.ncbi.nlm.nih.gov/pubmed/25258536 http://dx.doi.org/10.2147/NDT.S68670 |
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author | Aoki, Akiko Ishiguro, Shin Watanabe, Takashi Ueda, Mikito Hayashi, Yuki Akiyama, Kazufumi Kato, Kazuko Inoue, Yoshimasa Tsuchimine, Shoko Yasui-Furukori, Norio Shimoda, Kazutaka |
author_facet | Aoki, Akiko Ishiguro, Shin Watanabe, Takashi Ueda, Mikito Hayashi, Yuki Akiyama, Kazufumi Kato, Kazuko Inoue, Yoshimasa Tsuchimine, Shoko Yasui-Furukori, Norio Shimoda, Kazutaka |
author_sort | Aoki, Akiko |
collection | PubMed |
description | OBJECTIVE: The aims of the present study were to analyze the association between discontinuation of paroxetine (PAX) and the genetic variants of the polymorphism in the serotonin transporter gene-linked polymorphic region (5-HTTLPR) in Japanese patients with panic disorder (PD) and major depressive disorder (MDD). METHODS: The 5-HTTLPR genotype was determined by polymerase chain reaction method. PAX plasma concentration was measured by high-performance liquid chromatography to confirm adherence. RESULTS: When comparing between the PD and MDD patients with the chi-square test and Fisher’s exact test, the PD patients had a significant and higher discontinuation rate due to non-adherence than did the MDD patients (13.5% [7/52] versus 0% [0/88], respectively; P<0.001). MDD patients had a significant and higher discontinuation rate due to untraceability than PD patients (12.5% [11/88] versus 1.9% [1/52]; P=0.032). Multilogistic regression revealed a tendency for the long/short and short/short genotypes to affect discontinuation due to adverse effects in PD patients (25.0% versus 6.3%, respectively; P=0.054). CONCLUSION: The results indicate that the 5-HTTLPR genotype might contribute to the discontinuation of initial PAX treatment due to adverse effects in PD patients. |
format | Online Article Text |
id | pubmed-4174019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41740192014-09-25 Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder Aoki, Akiko Ishiguro, Shin Watanabe, Takashi Ueda, Mikito Hayashi, Yuki Akiyama, Kazufumi Kato, Kazuko Inoue, Yoshimasa Tsuchimine, Shoko Yasui-Furukori, Norio Shimoda, Kazutaka Neuropsychiatr Dis Treat Original Research OBJECTIVE: The aims of the present study were to analyze the association between discontinuation of paroxetine (PAX) and the genetic variants of the polymorphism in the serotonin transporter gene-linked polymorphic region (5-HTTLPR) in Japanese patients with panic disorder (PD) and major depressive disorder (MDD). METHODS: The 5-HTTLPR genotype was determined by polymerase chain reaction method. PAX plasma concentration was measured by high-performance liquid chromatography to confirm adherence. RESULTS: When comparing between the PD and MDD patients with the chi-square test and Fisher’s exact test, the PD patients had a significant and higher discontinuation rate due to non-adherence than did the MDD patients (13.5% [7/52] versus 0% [0/88], respectively; P<0.001). MDD patients had a significant and higher discontinuation rate due to untraceability than PD patients (12.5% [11/88] versus 1.9% [1/52]; P=0.032). Multilogistic regression revealed a tendency for the long/short and short/short genotypes to affect discontinuation due to adverse effects in PD patients (25.0% versus 6.3%, respectively; P=0.054). CONCLUSION: The results indicate that the 5-HTTLPR genotype might contribute to the discontinuation of initial PAX treatment due to adverse effects in PD patients. Dove Medical Press 2014-09-18 /pmc/articles/PMC4174019/ /pubmed/25258536 http://dx.doi.org/10.2147/NDT.S68670 Text en © 2014 Aoki 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 Aoki, Akiko Ishiguro, Shin Watanabe, Takashi Ueda, Mikito Hayashi, Yuki Akiyama, Kazufumi Kato, Kazuko Inoue, Yoshimasa Tsuchimine, Shoko Yasui-Furukori, Norio Shimoda, Kazutaka Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title | Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title_full | Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title_fullStr | Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title_full_unstemmed | Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title_short | Factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
title_sort | factors affecting discontinuation of initial treatment with paroxetine in panic disorder and major depressive disorder |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174019/ https://www.ncbi.nlm.nih.gov/pubmed/25258536 http://dx.doi.org/10.2147/NDT.S68670 |
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