Hu Ding-yuan, Shao Xiao-xiao, Xu Chang-long, Xia Sheng-long, Yu Li-qin, Jiang Li-jia, Jin Jie, Lin Xiu-qing, Jiang Yi
Department of Gastroenterology, Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
J Gastroenterol Hepatol. 2014 Oct;29(10):1778-85. doi: 10.1111/jgh.12599.
FUT2 and FUT3 genes are responsible for the formation of histo-blood group antigens, which act as binding sites for some intestinal microbes. Several studies suggested that FUT2 gene might affect the intestinal microbiota composition and modulate innate immune responses. However, the effect of FUT2 polymorphisms on Crohn's disease (CD) is uncertain. Our study aimed to analyze associations of CD with FUT2 and FUT3 polymorphisms in Chinese population.
A total of 273 CD patients and 479 controls were recruited. The genotypes of FUT2 (rs281377, rs1047781, and rs601338) and FUT3 (rs28362459, rs3745635, and rs3894326) were detected by SNaPshot analysis.
Compared with controls, homozygote TT of FUT2 (rs1047781) was significantly increased in CD patients (TT vs others; P = 0.002, odds ratio [OR] = 1.767, 95% confidence interval [CI] = 1.235-2.528). The haplotype TT formed with FUT2 (rs281377) and (rs1047781) was more prevalent in CD patients than in controls (48.9% vs 43.5%, P = 0.046). Mutant T allele and homozygote TT of FUT2 (rs1047781) were increased in colonic CD patients compared with controls (P < 0.001, OR = 1.843, 95% CI = 1.353-2.512; P < 0.001, OR = 2.607, 95% CI = 1.622-4.191, respectively). Although allele and genotypic distributions of FUT3 were not statistically different between CD patients and controls, mutant allele and genotype of FUT3 (rs28362459) and (rs3745635) were significantly discrepant in three subgroups of CD patients according to lesion locations (all P < 0.05).
Our study strongly implicates the polymorphic locus of FUT2 (rs1047781) in CD susceptibility in Chinese population. Mutations of FUT3 (rs28362459) and (rs3745635) might influence the lesion locations in CD patients.
FUT2和FUT3基因负责组织血型抗原的形成,这些抗原充当某些肠道微生物的结合位点。多项研究表明,FUT2基因可能影响肠道微生物群组成并调节先天免疫反应。然而,FUT2基因多态性对克罗恩病(CD)的影响尚不确定。我们的研究旨在分析中国人群中CD与FUT2和FUT3基因多态性的关联。
共招募了273例CD患者和479例对照。通过SNaPshot分析检测FUT2(rs281377、rs1047781和rs601338)和FUT3(rs28362459、rs3745635和rs3894326)的基因型。
与对照组相比,CD患者中FUT2(rs1047781)的纯合子TT显著增加(TT与其他基因型相比;P = 0.002,优势比[OR] = 1.767,95%置信区间[CI] = 1.235 - 2.528)。由FUT2(rs281377)和(rs1047781)形成的单倍型TT在CD患者中比在对照组中更普遍(48.9%对43.5%,P = 0.046)。与对照组相比,结肠CD患者中FUT2(rs1047781)的突变T等位基因和纯合子TT增加(P < 0.001,OR = 1.843,95% CI = 1.353 - 2.512;P < 0.001,OR = 2.607,95% CI = 1.622 - 4.191)。虽然CD患者和对照组之间FUT3的等位基因和基因型分布没有统计学差异,但根据病变部位,FUT3(rs28362459)和(rs3745635)的突变等位基因和基因型在CD患者的三个亚组中有显著差异(所有P < 0.05)。
我们的研究强烈提示FUT2(rs1047781)的多态性位点与中国人群的CD易感性有关。FUT3(rs28362459)和(rs3745635)的突变可能影响CD患者的病变部位。