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土耳其患者中CTLA-4(+49A/G)和NOD2/CARD15(N852S)基因多态性与炎症性肠病的关系

CTLA-4 (+49A/G) and NOD2/CARD15 (N852S) polymorphisms with inflammatory bowel disease in Turkish patients.

作者信息

Budak Diler Songül, Yaraş Serkan

机构信息

Department of Biotechnology, Faculty of Science and Letters, University of Niğde Ömer Halisdemir, 51240, Niğde, Turkey.

Department of Gastroenterology, Faculty of Medicine, University of Mersin, Mersin, Turkey.

出版信息

Cell Mol Biol (Noisy-le-grand). 2018 Aug 30;64(11):97-101.

Abstract

Crohn's disease (CD) and ulcerative colitis (UC) are the major types of inflammatory bowel disease (IBD) and exhibit similar clinical features and epidemiology. The main objective of this study was to analyze the correlation between the CTLA-4 gene +49A/G polymorphism and the NOD2/CARD15 gene N852S polymorphism in Turkish patients with IBD using polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) analysis. In this study, we evaluated the frequency of the CTLA-4 (+49A/G) and NOD2/CARD15 (N852S) polymorphisms in 62 patients with CD, 76 patients with UC, and 152 healthy individuals. The CTLA-4 and NOD2/CARD15 variants, rs231775 and rs104895467, were genotyped by PCR followed by RFLP. The results for the patients and the control group were statistically analyzed. According to our results, the CTLA-4 gene +49A/G polymorphism AA genotype was prevalent in CD patients and controls (29% vs 40%); the AG (56% vs 51%) and GG (15% vs 9%) genotypes were also observed. The prevalence of the of AA, AG and GG genotypes for the +49A/G polymorphism was 56%, 32% and 12%, respectively, in the UC patients, and 40%, 51% and 9%, respectively, in the healthy controls. In all subjects, just one band of 151 bp, corresponding to wild-type N852S, was found, and no other N852S mutant bands (151+129+22 and 129+22 bp) were detected using PCR-RFLP fragment electrophoresis.The CTLA-4 gene +49 A/G polymorphism and the NOD2/CARD15 gene N852S polymorphism were not associated with CD or UC in a Turkish population.

摘要

克罗恩病(CD)和溃疡性结肠炎(UC)是炎症性肠病(IBD)的主要类型,具有相似的临床特征和流行病学特点。本研究的主要目的是通过聚合酶链反应和限制性片段长度多态性(PCR-RFLP)分析,探讨土耳其IBD患者中细胞毒性T淋巴细胞相关抗原4(CTLA-4)基因+49A/G多态性与核苷酸结合寡聚化结构域2/胱天蛋白酶激活招募结构域15(NOD2/CARD15)基因N852S多态性之间的相关性。在本研究中,我们评估了62例CD患者、76例UC患者和152名健康个体中CTLA-4(+49A/G)和NOD2/CARD15(N852S)多态性的频率。通过PCR-RFLP对CTLA-4和NOD2/CARD15变异体rs231775和rs104895467进行基因分型。对患者和对照组的结果进行统计学分析。根据我们的结果,CTLA-4基因+49A/G多态性的AA基因型在CD患者和对照组中均较为常见(分别为29%和40%);也观察到AG(分别为56%和51%)和GG(分别为15%和9%)基因型。+49A/G多态性的AA、AG和GG基因型在UC患者中的患病率分别为56%、32%和12%,在健康对照组中分别为40%、51%和9%。在所有受试者中,仅发现一条对应野生型N852S的151 bp条带,使用PCR-RFLP片段电泳未检测到其他N852S突变条带(151+129+22和129+22 bp)。在土耳其人群中,CTLA-4基因+49 A/G多态性和NOD2/CARD15基因N852S多态性与CD或UC无关。

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