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溃疡性结肠炎患者队列中负责家族性地中海热(MEFV)的基因突变频率增加:潜在疾病修饰作用的证据?

Increased frequency of mutations in the gene responsible for familial Mediterranean fever (MEFV) in a cohort of patients with ulcerative colitis: evidence for a potential disease-modifying effect?

作者信息

Giaglis Stavros, Mimidis Konstantinos, Papadopoulos Vassilios, Thomopoulos Konstantinos, Sidiropoulos Prodromos, Rafail Stavros, Nikolopoulou Vassiliki, Fragouli Eleni, Kartalis Georgios, Tzioufas Athanasios, Boumpas Dimitrios, Ritis Konstantinos

机构信息

First Division of Internal Medicine, Democritus University of Thrace, Alexandroupolis, Greece.

出版信息

Dig Dis Sci. 2006 Apr;51(4):687-92. doi: 10.1007/s10620-006-3192-1.

Abstract

The MEFV gene, responsible for familial Mediterranean fever (FMF), is involved in inflammatory reactions through altered leukocyte apoptosis, secretion of interleukin (IL)-1beta, and activation of the NF-kappa B pathway. Ulcerative Colitis (UC) and FMF are both characterized by a recurrent pattern of presentation with periods of remission and flares associated with neutrophilic infiltration at the site of injury. The aim of this study was to investigate the possible correlation between UC and MEFV gene alterations. Twenty-five consecutive, first-diagnosed and untreated UC patients, 28 control patients with rheumatoid arthritis, and 65 normal individuals were analyzed. Nonisotopic RNase Cleavage Assay (NIRCA) was applied as a first-step mutational screening method of exons 10 and 2 of MEFV gene; direct sequencing was subsequently performed to confirm the results. MEFV mutations were identified in 7 (3 M694V/0, 2 M680I/0, 1 E148Q/E148Q, and 1 A744S/0) out of 25 UC patients versus 1 (M694V/0) out of 28 rheumatoid arthritis patients (P = .0199) and 1 (M694V/0) out of 65 healthy controls (P = .0004). Four out of 7 patients with MEFV mutations had inflammatory arthritis, a clinical finding that was not observed in the 18 UC patients with unmutated MEFV (P = .0028). Patients with UC almost universally carried the T A C G MEFV exon 2 haplotype in contrast with normal individuals (P < .0001) and FMF patients (P = .0310). In conclusion the increased frequency of mutations of MEFV in UC patients, especially in those with episodic arthritis, suggests a possible modifying effect of MEFV in the disease process and its localization within the joint. The difference in distribution of MEFV exon 2 haplotypes between UC patients and both FMF patients and normal individuals, suggests that UC patients constitute a genetically distinct population. Larger, longitudinal studies are needed to confirm these initial findings.

摘要

负责家族性地中海热(FMF)的MEFV基因通过改变白细胞凋亡、白细胞介素(IL)-1β的分泌以及核因子κB(NF-κB)途径的激活参与炎症反应。溃疡性结肠炎(UC)和FMF的特征均为呈复发模式,有缓解期和发作期,且发作期与损伤部位的中性粒细胞浸润有关。本研究的目的是调查UC与MEFV基因改变之间可能存在的相关性。对25例连续的初诊且未治疗的UC患者、28例类风湿关节炎对照患者和65例正常个体进行了分析。非同位素核糖核酸酶切割分析(NIRCA)作为MEFV基因第10外显子和第2外显子的第一步突变筛查方法;随后进行直接测序以确认结果。25例UC患者中有7例(3例M694V/0、2例M680I/0、1例E148Q/E148Q和1例A744S/0)检测到MEFV突变,而28例类风湿关节炎患者中有1例(M694V/0)(P = 0.0199),65例健康对照中有1例(M694V/0)(P = 0.0004)。7例携带MEFV突变的患者中有4例出现炎性关节炎,这一临床发现未在18例MEFV未突变的UC患者中观察到(P = 0.0028)。与正常个体(P < 0.0001)和FMF患者(P = 0.0310)相比,UC患者几乎普遍携带MEFV第2外显子的T A C G单倍型。总之,UC患者中MEFV突变频率增加,尤其是那些患有发作性关节炎的患者,提示MEFV在疾病过程及其在关节内的定位可能具有修饰作用。UC患者与FMF患者及正常个体之间MEFV第2外显子单倍型分布的差异,提示UC患者构成一个基因上独特的群体。需要开展更大规模的纵向研究来证实这些初步发现。

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