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Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population

BACKGROUND: Although familial clustering of functional dyspepsia (FD) has been reported, the role of genetics in the susceptibility to FD is still not well understood. In the present study, the association between serotonin transporter (SERT) gene (SLC6A4) polymorphism and FD was explored. METHODS:...

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Autores principales: Toyoshima, Fumihiko, Oshima, Tadayuki, Nakajima, Shigemi, Sakurai, Jun, Tanaka, Junji, Tomita, Toshihiko, Hori, Kazutoshi, Matsumoto, Takayuki, Miwa, Hiroto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142494/
https://www.ncbi.nlm.nih.gov/pubmed/21714874
http://dx.doi.org/10.1186/1471-2350-12-88
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author Toyoshima, Fumihiko
Oshima, Tadayuki
Nakajima, Shigemi
Sakurai, Jun
Tanaka, Junji
Tomita, Toshihiko
Hori, Kazutoshi
Matsumoto, Takayuki
Miwa, Hiroto
author_facet Toyoshima, Fumihiko
Oshima, Tadayuki
Nakajima, Shigemi
Sakurai, Jun
Tanaka, Junji
Tomita, Toshihiko
Hori, Kazutoshi
Matsumoto, Takayuki
Miwa, Hiroto
author_sort Toyoshima, Fumihiko
collection PubMed
description BACKGROUND: Although familial clustering of functional dyspepsia (FD) has been reported, the role of genetics in the susceptibility to FD is still not well understood. In the present study, the association between serotonin transporter (SERT) gene (SLC6A4) polymorphism and FD was explored. METHODS: Subjects were divided into either a postprandial distress syndrome (PDS) group or an epigastric pain syndrome (EPS) group according to the Rome III criteria. The healthy controls were those who had visited a hospital for an annual health check-up. The presence of the SLC6A4 promoter polymorphism, 5-hydroxytryptamin transporter gene linked polymorphic region (5-HTTLPR), was then evaluated, and logistic regression analysis was used to test all variables. RESULTS: The 5-HTTLPR genotype distribution was 448 SS, 174 SL, and 24 LL in controls and 30 SS, 20 SL, and 3 LL in FD subjects. No significant correlation was found between the 5-HTTLPR genotype and FD. When the genotypes and subtypes of FD were exploratory evaluated, the SL genotype was significantly associated with PDS [odds ratio (OR) = 2.24, 95% confidence interval (CI); 1.16-4.32, P = 0.034 after Bonferroni correction] compared to the SS genotype adjusted for sex and age. Comparison of the SS genotype with the SL/LL genotype also showed a significant association of genotype with PDS (OR = 2.32, 95% CI; 1.23-4.37, P = 0.009). CONCLUSION: The present results suggest that 5-HTTLPR L allele may influence the susceptibility to PDS.
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spelling pubmed-31424942011-07-24 Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population Toyoshima, Fumihiko Oshima, Tadayuki Nakajima, Shigemi Sakurai, Jun Tanaka, Junji Tomita, Toshihiko Hori, Kazutoshi Matsumoto, Takayuki Miwa, Hiroto BMC Med Genet Research Article BACKGROUND: Although familial clustering of functional dyspepsia (FD) has been reported, the role of genetics in the susceptibility to FD is still not well understood. In the present study, the association between serotonin transporter (SERT) gene (SLC6A4) polymorphism and FD was explored. METHODS: Subjects were divided into either a postprandial distress syndrome (PDS) group or an epigastric pain syndrome (EPS) group according to the Rome III criteria. The healthy controls were those who had visited a hospital for an annual health check-up. The presence of the SLC6A4 promoter polymorphism, 5-hydroxytryptamin transporter gene linked polymorphic region (5-HTTLPR), was then evaluated, and logistic regression analysis was used to test all variables. RESULTS: The 5-HTTLPR genotype distribution was 448 SS, 174 SL, and 24 LL in controls and 30 SS, 20 SL, and 3 LL in FD subjects. No significant correlation was found between the 5-HTTLPR genotype and FD. When the genotypes and subtypes of FD were exploratory evaluated, the SL genotype was significantly associated with PDS [odds ratio (OR) = 2.24, 95% confidence interval (CI); 1.16-4.32, P = 0.034 after Bonferroni correction] compared to the SS genotype adjusted for sex and age. Comparison of the SS genotype with the SL/LL genotype also showed a significant association of genotype with PDS (OR = 2.32, 95% CI; 1.23-4.37, P = 0.009). CONCLUSION: The present results suggest that 5-HTTLPR L allele may influence the susceptibility to PDS. BioMed Central 2011-06-29 /pmc/articles/PMC3142494/ /pubmed/21714874 http://dx.doi.org/10.1186/1471-2350-12-88 Text en Copyright ©2011 Toyoshima et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Toyoshima, Fumihiko
Oshima, Tadayuki
Nakajima, Shigemi
Sakurai, Jun
Tanaka, Junji
Tomita, Toshihiko
Hori, Kazutoshi
Matsumoto, Takayuki
Miwa, Hiroto
Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title_full Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title_fullStr Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title_full_unstemmed Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title_short Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population
title_sort serotonin transporter gene polymorphism may be associated with functional dyspepsia in a japanese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142494/
https://www.ncbi.nlm.nih.gov/pubmed/21714874
http://dx.doi.org/10.1186/1471-2350-12-88
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