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韩国肠易激综合征和功能性消化不良儿童的 5-羟色胺转运体基因和 G 蛋白β3 亚单位基因多态性。

Polymorphisms of the Serotonin Transporter Gene and G-Protein β3 Subunit Gene in Korean Children with Irritable Bowel Syndrome and Functional Dyspepsia.

机构信息

Department of Pediatrics, Eulji General Hospital, Eulji University College of Medicine, Seoul, Korea.

出版信息

Gut Liver. 2012 Apr;6(2):223-8. doi: 10.5009/gnl.2012.6.2.223. Epub 2012 Apr 17.

DOI:10.5009/gnl.2012.6.2.223
PMID:22570752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3343161/
Abstract

BACKGROUND/AIMS: Many candidate gene studies have revealed that polymorphisms of the 5'-flanking controlled SERT gene linked polymorphic region (5HTT-LPR) gene and G-protein β3 C825T gene might be associated with functional dyspepsia (FD) and irritable bowel syndrome (IBS). This study was performed to investigate polymorphisms of the 5HTT-LPR gene and G-protein β3 C825T gene in FD and IBS in Korean children.

METHODS

In total, 102 patients with FD, 72 patients with IBS based on the Rome III criteria and 148 healthy controls without gastrointestinal symptoms were included in the study to analyze 5HTT-LPR and G-protein β3 C825T polymorphisms.

RESULTS

5HTT-LPR genotype analysis revealed no signifi cant differences in FD and IBS patients compared with controls. The GNβ3 C825T genotype distribution for CC, CT, and TT was 23.6%, 53.4%, and 23.0% in controls, 36.3%, 38.2%, and 25.5% in FD and 37.5%, 38.9%, and 23.6% in IBS, respectively. The CC genotype was more common in FD and IBS patients than controls (p<0.05). When the IBS patients were grouped according to IBS subtypes, CC genotype GNβ3 C825T was common in diarrhea-dominant IBS, and the TT genotype was common in constipation-dominant IBS (p<0.05).

CONCLUSIONS

The CC genotype of G-protein β3 C825T may be associated with FD and diarrhea-predominant IBS. The TT genotype may be associated with constipation-predominant IBS.

摘要

背景/目的:许多候选基因研究表明,5'-侧翼控制 SERT 基因连接多态区(5-HTT-LPR)基因和 G 蛋白β3 C825T 基因的多态性可能与功能性消化不良(FD)和肠易激综合征(IBS)有关。本研究旨在探讨韩国儿童 FD 和 IBS 中 5-HTT-LPR 基因和 G 蛋白β3 C825T 基因的多态性。

方法

共纳入 102 例 FD 患者、72 例符合罗马 III 标准的 IBS 患者和 148 例无胃肠道症状的健康对照者,分析 5-HTT-LPR 和 G 蛋白β3 C825T 多态性。

结果

5-HTT-LPR 基因型分析显示,FD 和 IBS 患者与对照组无显著差异。CC、CT 和 TT 基因型在对照组、FD 和 IBS 中的分布分别为 23.6%、53.4%和 23.0%、36.3%、38.2%和 25.5%、37.5%、38.9%和 23.6%。CC 基因型在 FD 和 IBS 患者中比对照组更常见(p<0.05)。当根据 IBS 亚型对 IBS 患者进行分组时,CC 基因型 GNβ3 C825T 在腹泻型 IBS 中常见,而 TT 基因型在便秘型 IBS 中常见(p<0.05)。

结论

G 蛋白β3 C825T 的 CC 基因型可能与 FD 和腹泻型 IBS 有关。TT 基因型可能与便秘型 IBS 有关。

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G protein beta3 subunit, interleukin-10, and tumor necrosis factor-alpha gene polymorphisms in Koreans with irritable bowel syndrome.韩国肠易激综合征患者 G 蛋白β3 亚基、白细胞介素-10 和肿瘤坏死因子-α基因多态性。
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Gastroesophageal reflux disease is associated with the C825T polymorphism in the G-protein beta3 subunit gene (GNB3).胃食管反流病与G蛋白β3亚基基因(GNB3)中的C825T多态性相关。
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