Can Güray, Tezel Ahmet, Gürkan Hakan, Tozkır Hilmi, Ünsal Gülbin, Soylu Ali Rıza, Ümit Hasan Celalettin
Department of Gastroenterology, Abant İzzet Baysal University School of Medicine, Bolu, Turkey.
Turk J Gastroenterol. 2016 Nov;27(6):525-536. doi: 10.5152/tjg.2016.16327.
BACKGROUND/AIMS: Inflammatory bowel diseases are chronic, relapsing, inflammatory conditions. They have a genetic backround resulting in patient susceptibility. The aim of our study is to investigate the involvement of IL23R, JAK2, and STAT3 polymorphisms in inflammatory bowel diseases in a Turkish population.
Polymorphisms in IL23R (rs11209026), JAK2 (rs10758669), and STAT3 (rs3816769, rs2293152, rs744166, rs957970, rs8074524) were genotyped in 69 Crohn's disease patients, 157 ulcerative colitis patients, and 89 healthy controls.
The presence of (C) in rs10758669, (T) and (TT) in rs957970, and (TT) in rs744166 were found to increase the susceptibility to Crohn's disease (p=0.049, p=0.016, p=0.010, p=0.035, respectively), while rs2293152 (GC), rs744166 (CT), and rs957970 (CT) provide protection against Crohn's disease (p=0.007, p=0.043, p=0.043, respectively). While rs2293152 (GC) was protective, rs2293152 (CC) increased the susceptibility to ulcerative colitis (p=0.009, p=0.001). All the polymorphisms were associated with age-at-diagnosis, except rs11209026. Furthermore, rs2293152 was associated with an extension in ulcerative colitis, while rs10758669, rs3816769, rs744166, rs2293152, and rs957970 were associated with the subphenotype in Crohn's disease. The presence of rs10758669 (AC) was protective against perianal Crohn's disease (p=0.016). Additionally, rs10758669 and rs2293152 in Crohn's disease and rs8074524, rs3816769, and rs10758669 in ulcerative colitis were associated with the requirement of immunsuppression. Finally, rs8074524 and rs10758669 in Crohn's disease and rs11209026 in ulcerative colitis were associated with disease-related operation.
This is the first study of the single marker association of IL23R, JAK2, and STAT3 polymorphisms with ulcerative colitis and Crohn's disease in a Turkish population. It was demonstrated that these polymorphisms may be effective in the etiology of inflammatory bowel disease in this Turkish population.
背景/目的:炎症性肠病是慢性、复发性炎症性疾病。它们具有遗传背景,导致患者易感性增加。我们研究的目的是调查白细胞介素23受体(IL23R)、Janus激酶2(JAK2)和信号转导及转录激活因子3(STAT3)基因多态性在土耳其人群炎症性肠病中的作用。
对69例克罗恩病患者、157例溃疡性结肠炎患者和89例健康对照者进行IL23R(rs11209026)、JAK2(rs10758669)和STAT3(rs3816769、rs2293152、rs744166、rs957970、rs8074524)基因多态性基因分型。
发现rs10758669中(C)、rs957970中(T)和(TT)以及rs744166中(TT)的存在会增加患克罗恩病的易感性(p值分别为0.049、0.016、0.010、0.035),而rs2293152(GC)、rs744166(CT)和rs957970(CT)可预防克罗恩病(p值分别为0.007、0.043、0.043)。虽然rs2293152(GC)具有保护作用,但rs2293152(CC)会增加患溃疡性结肠炎的易感性(p值分别为0.009、0.001)。除rs11209026外,所有基因多态性均与确诊年龄相关。此外,rs2293152与溃疡性结肠炎的病变范围相关,而rs10758669、rs3816769、rs744166、rs2293152和rs957970与克罗恩病的亚型相关。rs10758669(AC)的存在可预防肛周克罗恩病(p = 0.016)。此外,克罗恩病中的rs1