首页> 外文期刊>Journal of clinical gastroenterology >Association of the -1438 G/A and 102 T/C Polymorphism of the 5-Ht2A Receptor Gene with Irritable Bowel Syndrome 5-Ht2A Gene Polymorphism in Irritable Bowel Syndrome.
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Association of the -1438 G/A and 102 T/C Polymorphism of the 5-Ht2A Receptor Gene with Irritable Bowel Syndrome 5-Ht2A Gene Polymorphism in Irritable Bowel Syndrome.

机译:5-Ht2A受体基因的-1438 G / A和102 T / C多态性与肠易激综合症的相关性5-Ht2A基因多态性与肠易激综合症的关联。

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GOALS:: The aim of this study is to investigate whether there were any association between the 102 T/C and -1438 G/A polymorphisms of the 5-HT2A receptor gene and IBS, and abdominal pain, anxiety and depression. BACKGROUND:: Genes involved in serotonin (5-HT) metabolism are good candidates for the pathogenesis of irritable bowel syndrome (IBS). Recently, a silent polymorphism in the 5-HT2A receptor gene was identified that is defined by a T to C transition at position 102. Also, a novel G to A base change at position -1438 of the promoter region has been detected in 5-HT2A receptor gene. STUDY:: Fifty-four patients with IBS diagnosed according to the Rome 1 criteria and 107 healthy individuals were included in the study. PCR was used to amplify a 468-bp (G-->A) and 342-bp (T-->C) fragment of genomic DNA containing the polymorphism. Hospital anxiety and depression scale was used to assess the risk of depression and anxiety. Severity of chronic abdominal pain was determined by visual analogue scale (VAS). RESULTS:: It was shown that there was a high incidence of homozygote C allele of the 102T/C polymorphism (%22.2; OR: 7.89, P = 0.04) and homozygote A allele of the -1438 G/A promoter region (%%37; OR: 11.14, P = 0.01) in patients with IBS. The risk of having an anxiety disorder was 83.3% in patients with C/C genotype, which was higher than other allele carrying patients, and overall mean (%52.7). (chi = 8.56, P = 0.014). The patients with T/T genotype had a VAS score of 54.93 +/- 2.59 mm, which was significantly higher than that of the patients with other genotypes (p1 = 0.02, p2 = 0.001). CONCLUSION:: This study suggests that the patients with homozygote C allele of the 102 T/C polymorphisms or homozygote A allele of the -1438 G/A polymorphism of the 5-HT2A receptor gene, have a high risk of IBS. On the other hand, T/T genotype of 102 T/C polymorphism may be associated with more severe pain in patient with IBS.
机译:目标:该研究的目的是调查5-HT2A受体基因和IBS的102 T / C和-1438 G / A多态性与腹痛,焦虑和抑郁之间是否存在关联。背景:参与5-羟色胺(5-HT)代谢的基因是肠易激综合征(IBS)发病的良好候选者。最近,鉴定了5-HT2A受体基因的沉默多态性,该沉默多态性由位置102处的T到C过渡所定义。此外,在启动子区域的-1438位置上新的G到A碱基变化已被检测到。 HT2A受体基因。研究::根据罗马1标准诊断的54例IBS患者和107名健康个体被纳入研究。 PCR用于扩增包含多态性的基因组DNA的468bp(G→A)和342bp(T→C)片段。医院焦虑和抑郁量表用于评估抑郁和焦虑的风险。慢性腹痛的严重程度由视觉模拟量表(VAS)确定。结果:显示102T / C多态性的纯合子C等位基因(%22.2; OR:7.89,P = 0.04)和-1438 G / A启动子区域的纯合子A等位基因(%%)的发生率很高37; OR:11.14,P = 0.01)。 C / C基因型患者发生焦虑症的风险为83.3%,高于其他携带等位基因的患者和总体平均值(%52.7)。 (chi = 8.56,P = 0.014)。 T / T基因型患者的VAS评分为54.93 +/- 2.59 mm,明显高于其他基因型患者(p1 = 0.02,p2 = 0.001)。结论:这项研究表明,具有102 T / C多态性的纯合子C等位基因或5-HT2A受体基因的-1438 G / A多态性的纯合子A等位基因患者IBS的风险较高。另一方面,IBS患者的102 T / C多态性的T / T基因型可能与更严重的疼痛有关。

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