Department of Gastroenterology, Inflammatory Bowel Disease Clinic, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán.
J Clin Gastroenterol. 2011 Jul;45(6):531-5. doi: 10.1097/MCG.0b013e3181faec51.
Ulcerative colitis (UC) is an inflammatory bowel disease of unknown etiology. Among cytokines induced in UC, interleukin 1 antagonist (IL-1ra) and interleukin 1 β (IL-1β) seems to have a central role because of its immunoregulatory and proinflammatory activities.
To determine the association between IL-1RA and IL-1B gene polymorphisms and the clinical features of UC in the Mexican Mestizo population.
Five polymorphisms in the IL-1 gene cluster members IL-1B (rs16944), IL1F10 (rs3811058), and IL-1RN (rs419598, rs315952, and rs315951) were genotyped by 5' exonuclease TaqMan genotyping assays in a group of 200 Mexican patients with UC and 248 ethnically matched unrelated healthy controls.
We found a significant increased frequencies of IL-1RN6/1 TC (rs315952) and RN6/2 CC (rs315951) and decreased frequency of IL-1B-511 TC (rs16944) genotypes in UC patients as compared with healthy controls. In the subgroup analysis, we found a significant association between the RN6/2 GG (rs315951) and IL-1B-511 CC (rs16944) genotypes and the presence of steroid-dependence in UC patients (pC=00001, OR=15.6 and pC=0.008, OR=4.09, respectively). Patients with UC showed increased frequencies of IL-1RN "CTC" and "TCG" haplotypes when compared with healthy controls (P=0.019, OR=1.43 and P<10(-7), OR=2.63, respectively). Two haplotypes (TTG and CTG) showed decreased frequency in patients when compared with healthy controls (P=9×10(-7), OR=0.11 and P=8×10(-6), OR=0.11, respectively).
IL-1 RN and IL-1B polymorphisms were associated with the genetic susceptibility to develop UC and might be associated with the presence of steroid-dependence in UC patients.
溃疡性结肠炎(UC)是一种病因不明的炎症性肠病。在 UC 诱导的细胞因子中,白细胞介素 1 拮抗剂(IL-1ra)和白细胞介素 1β(IL-1β)似乎具有核心作用,因为它们具有免疫调节和促炎活性。
确定白细胞介素 1 受体拮抗剂(IL-1ra)和白细胞介素 1β(IL-1β)基因多态性与墨西哥梅斯蒂索人溃疡性结肠炎临床特征之间的关系。
通过 5'外切酶 TaqMan 基因分型检测,对 200 例墨西哥 UC 患者和 248 名种族匹配的无关健康对照者的白细胞介素基因簇成员白细胞介素 1B(rs16944)、白细胞介素 1F10(rs3811058)和白细胞介素 1RN(rs419598、rs315952 和 rs315951)中的 5 个多态性进行基因分型。
与健康对照组相比,UC 患者中 IL-1RN6/1TC(rs315952)和 RN6/2CC(rs315951)的频率显著升高,而 IL-1B-511TC(rs16944)的频率显著降低。在亚组分析中,我们发现 UC 患者中 RN6/2GG(rs315951)和 IL-1B-511CC(rs16944)基因型与类固醇依赖的存在之间存在显著关联(pC=0.001,OR=15.6;pC=0.008,OR=4.09)。与健康对照组相比,UC 患者的 IL-1RN“CTC”和“TCG”单倍型频率升高(P=0.019,OR=1.43;P<10(-7),OR=2.63)。与健康对照组相比,两种单倍型(TTG 和 CTG)的频率降低(P=9×10(-7),OR=0.11;P=8×10(-6),OR=0.11)。
白细胞介素 1RN 和白细胞介素 1B 多态性与 UC 的遗传易感性相关,并且可能与 UC 患者类固醇依赖的存在相关。