Association Study of Common Genetic Variants in Pre-microRNAs in Patients with Ulcerative Colitis

被引:73
|
作者
Okubo, Masaaki [1 ]
Tahara, Tomomitsu [1 ]
Shibata, Tomoyuki [1 ]
Yamashita, Hiromi [1 ]
Nakamura, Masakatsu [1 ]
Yoshioka, Daisuke [1 ]
Yonemura, Joh [1 ]
Kamiya, Yoshio [1 ]
Ishizuka, Takamitsu [1 ]
Nakagawa, Yoshihito [1 ]
Nagasaka, Mitsuo [1 ]
Iwata, Masami [1 ]
Yamada, Hideto [2 ]
Hirata, Ichiro [1 ]
Arisawa, Tomiyasu [2 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Gastroenterol, Aichi 4701192, Japan
[2] Kanazawa Med Univ, Dept Gastroenterol, Uchinada, Ishikawa 9200293, Japan
关键词
Pre-microRNAs; ulcerative colitis; polymorphism; rs11614913; rs2910164; rs3746444; miR-196a2; miR-146a; miR-499; LUNG-CANCER; POLYMORPHISM; DISEASE; SUSCEPTIBILITY; EXPRESSION; LOCI; RNAS;
D O I
10.1007/s10875-010-9461-y
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Common single-nucleotide polymorphisms (SNPs) in microRNAs (miRNA) have been shown to be associated with susceptibility to several human diseases. We evaluated the associations of three SNPs (rs11614913, rs2910164, and rs3746444) in pre-miRNAs (miR-196a2, miR-146a, and miR-499) with the risk of ulcerative colitis (UC) in a Japanese population. The rs11614913 (T > C), rs2910164 (C > G), and rs3746444 (A > G) SNPs were genotyped in 170 UC and 403 control subjects. The rs3746444 AG genotype was significantly higher among the UC group (odds ratio (OR) = 1.51, 95% CI = 1.03-2.21, p = 0.037). The rs3746444 AG genotype was associated with onset at an older age (OR = 1.70, 95% CI = 1.04-2.78, p = 0.035), left-sided colitis and pancolitis (left-sided colitis, OR = 2.10, 95% CI = 1.12-3.94, p = 0.024; pancolitis, OR = 1.81, 95% CI = 1.09-3.01, p = 0.028, left-sided colitis + pancolitis, OR = 1.91, 95% CI = 1.26-2.92, p = 0.003), higher number of times hospitalized (OR = 2.63, 95% CI = 1.22-5.69, p = 0.017), steroid dependence (OR = 2.63, 95% CI = 1.27-5.44, p = 0.014), and refractory phenotypes (OR = 2.76, 95% CI = 1.46-5.21, p = 0.002) while the rs3746444 AA genotype was inversely associated with the number of times hospitalized (2 similar to, OR = 0.36, 95% CI = 0.17-0.79, p = 0.012), steroid dependence (OR = 0.42, 95% CI = 0.21-0.88, p = 0.021), and refractory phenotypes (OR = 0.38, 95% CI = 0.20-0.72, p = 0.003). The rs1161913 TT genotype also held a significantly higher risk of refractory phenotype (T/T vs. T/C + C/C, OR = 2.21, 95% CI = 1.17-4.18, p = 0.016). Our results provided the first evidence that rs3746444 SNP may influence the susceptibility to UC, and both rs3746444 and rs11614913 SNPs may influence the pathophysiological features of UC.
引用
收藏
页码:69 / 73
页数:5
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