Suppr超能文献

消化不良症状患者中血清素-2A受体基因T102C多态性

Serotonin-2A receptor gene T102C polymorphism in patients with dyspeptic symptoms.

作者信息

Tahara Tomomitsu, Arisawa Tomiyasu, Shibata Tomoyuki, Nakamura Masakatsu, Wang Fangyu, Hirata Ichiro, Nakano Hiroshi

机构信息

Department of Gastroenterology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.

出版信息

Hepatogastroenterology. 2008 Sep-Oct;55(86-87):1921-4.

Abstract

BACKGROUND/AIMS: The role of genetics in the susceptibility to functional dyspepsia (FD) is unclear. Serotonin (5-HT) is expressed in gastro-intestinal tract and modulates the sensory-motor functions in the digestive tract. Genetic association has been reported between C102T polymorphism in the gene encoding 5-HT 2A receptor (5HTR2A) and various diseases. We aimed to clarify the association between 5HTR2A C102T polymorphism and dyspeptic symptom in a Japanese population.

METHODOLOGY

91 dyspeptics and 93 non-dyspeptic subjects enrolled in this study. Dyspeptic symptoms were divided into 9 categories. 5HTR2A gene T102C polymorphism was determined by polymerase chain reaction-restriction fragment length polymorphism.

RESULTS

In the non-dyspeptics, the 5HTR2A geno type distribution was 21TT (22.6%), 50TC (53.8%), and 22CC (23.6%). Meanwhile, the 5HTR2A genotype distribution in dyspeptics was 30 TT (33.0%), 40 TC (43.9%), and 21 CC (23.1%). There was no significant difference between the two groups in the genotype distribution. We did not find any association between 5HTR2A genotypes and dyspeptic patients in different gender and H. pylori infection status. Also, no correlation was found between 5HTR2A polymorphism and any of the 9 different dyspeptic symptoms.

CONCLUSIONS

Our results suggest that 5HTR2A polymorphism is unlikely to be associated with susceptibility of dyspeptic symptoms. The role of genetics to the development of dyspepsia needs further evaluation.

摘要

背景/目的:遗传学在功能性消化不良(FD)易感性中的作用尚不清楚。血清素(5-羟色胺,5-HT)在胃肠道中表达,并调节消化道的感觉运动功能。据报道,5-HT 2A受体(5HTR2A)编码基因中的C102T多态性与多种疾病之间存在遗传关联。我们旨在阐明日本人群中5HTR2A C102T多态性与消化不良症状之间的关联。

方法

91名消化不良患者和93名非消化不良受试者参与了本研究。消化不良症状分为9类。通过聚合酶链反应-限制性片段长度多态性测定5HTR2A基因T102C多态性。

结果

在非消化不良患者中,5HTR2A基因型分布为21例TT(22.6%)、50例TC(53.8%)和22例CC(23.6%)。同时,消化不良患者中5HTR2A基因型分布为30例TT(33.0%)、40例TC(43.9%)和21例CC(23.1%)。两组间基因型分布无显著差异。我们未发现5HTR2A基因型与不同性别及幽门螺杆菌感染状态的消化不良患者之间存在任何关联。此外,未发现5HTR2A多态性与9种不同消化不良症状中的任何一种存在相关性。

结论

我们的结果表明,5HTR2A多态性不太可能与消化不良症状的易感性相关。遗传学在消化不良发生发展中的作用需要进一步评估。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验