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Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients

The serotonin [5-hydroxytryptamine (5-HT)] system has been implicated in the pathogenesis of major depressive disorder (MDD). Among the 5-HT receptor subtypes, 5-HT2 is one of the major pharmacological therapeutic targets for MDD. There have been inconsistent findings in previous pharmacogenetic stu...

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Autores principales: Kao, Chung-Feng, Kuo, Po-Hsiu, Yu, Younger W.-Y., Yang, Albert C., Lin, Eugene, Liu, Yu-Li, Tsai, Shih-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845659/
https://www.ncbi.nlm.nih.gov/pubmed/33519430
http://dx.doi.org/10.3389/fphar.2020.559601
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author Kao, Chung-Feng
Kuo, Po-Hsiu
Yu, Younger W.-Y.
Yang, Albert C.
Lin, Eugene
Liu, Yu-Li
Tsai, Shih-Jen
author_facet Kao, Chung-Feng
Kuo, Po-Hsiu
Yu, Younger W.-Y.
Yang, Albert C.
Lin, Eugene
Liu, Yu-Li
Tsai, Shih-Jen
author_sort Kao, Chung-Feng
collection PubMed
description The serotonin [5-hydroxytryptamine (5-HT)] system has been implicated in the pathogenesis of major depressive disorder (MDD). Among the 5-HT receptor subtypes, 5-HT2 is one of the major pharmacological therapeutic targets for MDD. There have been inconsistent findings in previous pharmacogenetic studies investigating the antidepressant therapeutic response using one or several 5-HT2A (HTR2A) genetic polymorphisms. By using gene-based association analysis, we hope to identify genetic variants of HTR2A which are related to MDD susceptibility and its antidepressant therapeutic response. 288 HTR2A single nucleotide polymorphisms in MDD susceptibility have been investigated through a case–control (455 MDD patients and 2, 998 healthy controls) study, as well as in antidepressant efficacy (n = 455) in our current research. The 21-item Hamilton Rating Scale for Depression was used to evaluate measures of antidepressant therapeutic efficacy. From two MDD groups in the antidepressant therapeutic response, by using gene-based analyses, we have identified 14 polymorphisms as suggestive markers for therapeutic response (13 for remission and 1 for response) in both meta- and mega-analyses. All of these HTR2A reported polymorphisms did not reach statistical significance in the case–control association study. This current investigation supported the link between HTR2A variants and antidepressant therapeutic response in MDD but not with MDD susceptibility.
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spelling pubmed-78456592021-01-30 Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients Kao, Chung-Feng Kuo, Po-Hsiu Yu, Younger W.-Y. Yang, Albert C. Lin, Eugene Liu, Yu-Li Tsai, Shih-Jen Front Pharmacol Pharmacology The serotonin [5-hydroxytryptamine (5-HT)] system has been implicated in the pathogenesis of major depressive disorder (MDD). Among the 5-HT receptor subtypes, 5-HT2 is one of the major pharmacological therapeutic targets for MDD. There have been inconsistent findings in previous pharmacogenetic studies investigating the antidepressant therapeutic response using one or several 5-HT2A (HTR2A) genetic polymorphisms. By using gene-based association analysis, we hope to identify genetic variants of HTR2A which are related to MDD susceptibility and its antidepressant therapeutic response. 288 HTR2A single nucleotide polymorphisms in MDD susceptibility have been investigated through a case–control (455 MDD patients and 2, 998 healthy controls) study, as well as in antidepressant efficacy (n = 455) in our current research. The 21-item Hamilton Rating Scale for Depression was used to evaluate measures of antidepressant therapeutic efficacy. From two MDD groups in the antidepressant therapeutic response, by using gene-based analyses, we have identified 14 polymorphisms as suggestive markers for therapeutic response (13 for remission and 1 for response) in both meta- and mega-analyses. All of these HTR2A reported polymorphisms did not reach statistical significance in the case–control association study. This current investigation supported the link between HTR2A variants and antidepressant therapeutic response in MDD but not with MDD susceptibility. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7845659/ /pubmed/33519430 http://dx.doi.org/10.3389/fphar.2020.559601 Text en Copyright © 2020 Kao, Kuo, Yu, Yang, Lin, Liu and Tsai. 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 Pharmacology
Kao, Chung-Feng
Kuo, Po-Hsiu
Yu, Younger W.-Y.
Yang, Albert C.
Lin, Eugene
Liu, Yu-Li
Tsai, Shih-Jen
Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title_full Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title_fullStr Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title_full_unstemmed Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title_short Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients
title_sort gene-based association analysis suggests association of htr2a with antidepressant treatment response in depressed patients
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845659/
https://www.ncbi.nlm.nih.gov/pubmed/33519430
http://dx.doi.org/10.3389/fphar.2020.559601
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