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白细胞介素12 C(-1188)A多态性与肠易激综合征之间无关联。

Lack of Association between Interleukin 12 C(-1188)A Polymorphism and Irritable Bowel Syndrome.

作者信息

Barkhordari Elham, Amirzargar Ali Akbar, Ebrahimi-Daryani Naser, Mahmoudi Mahdi, Ansaripour Bita, Alighardashi Maryam, Ahmadi-Ashtiani Hamid Reza, Bashashati Mohammad, Rezaei Nima

机构信息

Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Avicenna J Med Biotechnol. 2011 Jan;3(1):45-8.

Abstract

Irritable Bowel Syndrome (IBS) is a functional gastrointestinal disorder, characterized by recurrent abdominal pain and altered bowel habits. This study was performed to investigate the important role of interleukin-12 (IL-12) in intestinal inflammation. For this study seventy one patients with IBS and 140 controls were investigated. The allele and genotype frequencies of IL-12 C(-1188)A were determined using polymerase chain reaction with sequence-specific primers. The allele A was more common that the allele C in both groups of patients and controls. There was not any significant difference on IL-12 alleles and genotypes between patients and controls. The AA genotype was the most common genotypes, which was seen in 57.4% of the patients and 51.4% of the controls (p = 0.53). Although frequency of the CC genotype in the control group was lower than the patient group, this difference was not significant (5.7% vs. 11.5%, respectively, p = 0.16). Considering the lack of association between IL-12 C(-1188)A polymorphism and IBS, this cytokine gene polymorphism may not have significant role in the pathophysiology of disease.

摘要

肠易激综合征(IBS)是一种功能性胃肠疾病,其特征为反复出现腹痛和排便习惯改变。本研究旨在探讨白细胞介素-12(IL-12)在肠道炎症中的重要作用。在本研究中,对71例肠易激综合征患者和140名对照者进行了调查。采用序列特异性引物聚合酶链反应测定IL-12 C(-1188)A的等位基因和基因型频率。在患者组和对照组中,等位基因A比等位基因C更常见。患者和对照组之间的IL-12等位基因和基因型没有任何显著差异。AA基因型是最常见的基因型,在57.4%的患者和51.4%的对照者中出现(p = 0.53)。虽然对照组中CC基因型的频率低于患者组,但这种差异并不显著(分别为5.7%和11.5%,p = 0.16)。考虑到IL-12 C(-1188)A多态性与肠易激综合征之间缺乏关联,这种细胞因子基因多态性可能在该疾病的病理生理学中没有显著作用。

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