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NFKB1 基因(编码核因子-κB)的 -449 C>G 多态性与溃疡性结肠炎易感性有关。

-449 C>G polymorphism of NFKB1 gene, coding nuclear factor-kappa-B, is associated with the susceptibility to ulcerative colitis.

机构信息

Department of Gastroenterology, Kanazawa Medical University, Ishikawa 920-0293, Japan.

出版信息

World J Gastroenterol. 2012 Dec 21;18(47):6981-6. doi: 10.3748/wjg.v18.i47.6981.

Abstract

AIM

To clarify the association between a polymorphism -449 C>G (rs72696119) in 5'-UTR of NFKB1 with ulcerative colitis (UC).

METHODS

The studied population comprised 639 subjects, including patients with UC (UC cases, n = 174) and subjects without UC (controls, n = 465). We employed polymerase chain reaction-single strand conformation polymorphism to detect the gene polymorphism.

RESULTS

The rs72696119 G allele frequencies in controls and UC cases were 33.4% and 38.5%, respectively (P = 0.10). Genotype frequency of the GG homozygote in UC cases was significantly higher than that in controls (P = 0.017), and the GG homozygote was significantly associated with susceptibility to UC [odds ratio (OR), 1.88; 95%CI, 1.13-3.14]. In male subjects, the GG homozygote was associated with an increased risk for UC (OR, 3.10; 95%CI, 1.47-6.54; P = 0.0053), whereas this association was not found in female subjects. In addition, the GG homozygote was significantly associated with the risk of non-continuous disease (OR, 2.06; 95%CI, 1.12-3.79; P = 0.029), not having total colitis (OR, 2.40; 95%CI, 1.09-3.80, P = 0.040), disease which developed before 20 years of age (OR, 2.80; 95%CI, 1.07-7.32, P = 0.041), no hospitalization (OR, 2.28; 95%CI, 1.29-4.05; P = 0.0090) and with a maximum of 8 or less on the UCDAI score (OR, 2.45; 95%CI, 1.23-4.93; P = 0.022).

CONCLUSION

Our results provide evidence that NFKB1 polymorphism rs72696119 was significantly associated with the development of UC. This polymorphism influences the susceptibility to and pathophysiological features of UC.

摘要

目的

阐明 NFKB1 5'-UTR 中的 -449 C>G(rs72696119)多态性与溃疡性结肠炎(UC)之间的关联。

方法

研究人群包括 639 名受试者,包括 UC 患者(UC 病例,n=174)和无 UC 受试者(对照,n=465)。我们采用聚合酶链反应-单链构象多态性检测基因多态性。

结果

对照组和 UC 病例的 rs72696119 G 等位基因频率分别为 33.4%和 38.5%(P=0.10)。UC 病例中 GG 纯合子的基因型频率明显高于对照组(P=0.017),且 GG 纯合子与 UC 的易感性显著相关[比值比(OR),1.88;95%可信区间,1.13-3.14]。在男性受试者中,GG 纯合子与 UC 风险增加相关(OR,3.10;95%可信区间,1.47-6.54;P=0.0053),而在女性受试者中未发现这种关联。此外,GG 纯合子与非连续性疾病的风险显著相关(OR,2.06;95%可信区间,1.12-3.79;P=0.029),与无全结肠炎(OR,2.40;95%可信区间,1.09-3.80,P=0.040)、20 岁前发病(OR,2.80;95%可信区间,1.07-7.32,P=0.041)、无住院治疗(OR,2.28;95%可信区间,1.29-4.05;P=0.0090)和 UCDAI 评分最高为 8 或更低(OR,2.45;95%可信区间,1.23-4.93;P=0.022)相关。

结论

我们的结果提供了证据表明,NFKB1 多态性 rs72696119 与 UC 的发生显著相关。这种多态性影响 UC 的易感性和病理生理特征。

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