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肠易激综合征中的促炎细胞因子基因多态性。

Proinflammatory cytokine gene polymorphisms in irritable bowel syndrome.

机构信息

Department of Gastroenterology and Hepatology, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

J Clin Immunol. 2010 Jan;30(1):74-9. doi: 10.1007/s10875-009-9342-4. Epub 2009 Oct 21.

Abstract

INTRODUCTION

Irritable bowel syndrome (IBS) is a multifactorial functional gastrointestinal disorder, characterized by recurrent abdominal pain and altered bowel habits. Proinflammatory cytokines can play an important role in intestinal inflammation, while their production is under genetic control.

METHODS

This study was performed in a group of patients with IBS to analyze the genotype frequencies of a number polymorphic genes coding for proinflammatory cytokine (interleukin-6 (IL), tumor necrosis factor-alpha (TNF-alpha), and IL-1 group). Using polymerase chain reaction with sequence-specific primers method, the cytokine genes were amplified, and alleles and genotypes of 71 patients with IBS were detected on gel electrophoresis, and the results were compared with healthy control subjects.

RESULTS

Results of the analyzed data showed that the frequencies IL-1R C allele at position Pst-I 1970 (P = 0.017), IL-6 G allele at position -174 (P = 0.002), and TNF-alpha G allele at position -238 (P < 0.001) in the patient group were significantly higher than the control group. IL-6 GG genotype (-174) and TNF-alpha GG genotype (-238) in the patient group were also significantly overrepresented (P < 0.001), while IL-6 CG genotype (-174) and TNF-alpha GA genotype (-238) were significantly decreased in the patients with IBS (P < 0.001). The frequencies of IL-6 (-174, nt565) GG haplotype and TNF-alpha (-308, -238) GG haplotype were also significantly higher in the patient group (P < 0.001), whereas the frequencies of the haplotypes IL-6 CG and TNF-alpha GA were significantly decreased in the patients with IBS (P < 0.001).

CONCLUSION

IL-6 and TNF-alpha proinflammatory cytokine gene polymorphisms could change individual susceptibility to IBS and might have a role in pathophysiology of disease.

摘要

简介

肠易激综合征(IBS)是一种多因素的功能性胃肠道疾病,其特征为反复发作的腹痛和排便习惯改变。促炎细胞因子在肠道炎症中起着重要作用,而其产生受遗传控制。

方法

本研究在一组 IBS 患者中进行,以分析编码促炎细胞因子(白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和 IL-1 组)的一些多态性基因的基因型频率。采用聚合酶链反应与序列特异性引物法,扩增细胞因子基因,在凝胶电泳上检测 71 例 IBS 患者的等位基因和基因型,并与健康对照组进行比较。

结果

分析数据的结果表明,患者组中位于 Pst-I 1970 位的 IL-1R C 等位基因(P = 0.017)、位于-174 位的 IL-6 G 等位基因(P = 0.002)和位于-238 位的 TNF-α G 等位基因(P < 0.001)的频率明显高于对照组。患者组中 IL-6 GG 基因型(-174)和 TNF-α GG 基因型(-238)也明显过多(P < 0.001),而 IBS 患者中 IL-6 CG 基因型(-174)和 TNF-α GA 基因型(-238)明显减少(P < 0.001)。IL-6(-174,nt565)GG 单倍型和 TNF-α(-308,-238)GG 单倍型的频率在患者组中也明显升高(P < 0.001),而 IL-6 CG 和 TNF-α GA 单倍型的频率在 IBS 患者中明显降低(P < 0.001)。

结论

IL-6 和 TNF-α促炎细胞因子基因多态性可能改变个体对 IBS 的易感性,并可能在疾病的病理生理学中起作用。

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