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巨噬细胞移动抑制因子(MIF)基因启动子多态性与胆道闭锁患者纤维化增加相关,但与疾病易感性无关。

Macrophage Migration Inhibitory Factor (MIF) Gene Promotor Polymorphism Is Associated with Increased Fibrosis in Biliary Atresia Patients, but Not with Disease Susceptibility.

作者信息

Sadek Khaled H, Ezzat Sameera, Abdel-Aziz Samira A, Alaraby Hanaa, Mosbeh Asmaa, Abdel-Rahman Mohamed H

机构信息

Immunogenetics Department, Division of Human Genetics and Genome Research, National Research Centre, Shebin Elkom, Menoufiya, Egypt.

Department of Ophthalmology, The Ohio State University, Columbus, Ohio, USA.

出版信息

Ann Hum Genet. 2017 Sep;81(5):177-183. doi: 10.1111/ahg.12199. Epub 2017 Jun 28.

Abstract

Two polymorphisms, rs755622 and rs5844572, in the promoter region of the macrophage migration inhibitory factor (MIF) gene influence the basal and/or induced transcriptional activity and have been linked to several inflammatory and autoimmune diseases. The aim of this study was to investigate the association between these two polymorphisms and disease susceptibility in patients with biliary atresia (BA). Allele frequencies of rs755622 and rs5844572 were assessed in 60 Egyptian infants with a confirmed diagnosis of BA. DNA was extracted from archival material. For the rs755622, samples were tested using Taqman real-time PCR, and for the rs5844572, samples were tested using fluorescence-based genotyping. The allele frequency in the general population was assessed in 141 healthy adults from the same geographical location. No statistical differences were observed in the allele frequencies of either rs755622 or rs5844572 between BA patients and controls. The homozygous and heterozygous short repeats (5/5, or 5/X) of rs5844572 were observed more frequently (16/28, 57.1%) in BA patients with mild to moderate fibrosis compared with those with marked fibrosis (10/32, 31.3%). The difference was statistically significant (P  =  0.032). In conclusion, we observed no association between MIF rs755622 and rs5844572 polymorphisms and susceptibility to BA; however, the rs5844572 could be linked to the rate of progression of the disease and extent of fibrosis.

摘要

巨噬细胞移动抑制因子(MIF)基因启动子区域的两个多态性位点rs755622和rs5844572,会影响基础转录活性和/或诱导转录活性,并且与多种炎症和自身免疫性疾病相关。本研究旨在探讨这两个多态性位点与胆道闭锁(BA)患者疾病易感性之间的关联。对60例确诊为BA的埃及婴儿进行rs755622和rs5844572的等位基因频率评估。DNA从存档材料中提取。对于rs755622,使用Taqman实时PCR检测样本;对于rs5844572,使用基于荧光的基因分型检测样本。在来自同一地理位置的141名健康成年人中评估一般人群的等位基因频率。BA患者与对照组之间,rs755622或rs5844572的等位基因频率均未观察到统计学差异。与重度纤维化的BA患者(10/32,31.3%)相比,轻度至中度纤维化的BA患者中rs5844572的纯合子和杂合子短重复序列(5/5,或5/X)的观察频率更高(16/28,57.1%)。差异具有统计学意义(P = 0.032)。总之,我们观察到MIF基因的rs755622和rs5844572多态性与BA易感性之间无关联;然而,rs5844572可能与疾病进展速度和纤维化程度有关。

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