Department of Neurosurgery, Air Force General Hospital of the Chinese PLA, 30 Fucheng Road, Haidian District, Beijing 100142, China.
Gene. 2013 Sep 10;526(2):228-31. doi: 10.1016/j.gene.2013.05.012. Epub 2013 May 23.
A variety of epidemiologic studies have focused on the association between macrophage migration inhibitory factor (MIF) gene--173G/C polymorphism and inflammatory bowel disease (IBD). However, results in different studies have been inconsistent. In order to derive a more precise estimation of the associations, we performed this meta-analysis and systematic searches of electronic databases PubMed and Web of Science (up to April 30, 2013). Based on our search criteria, a total of seven eligible studies concerning the MIF--173G/C polymorphism and IBD risk were included in the final meta-analysis, comprising 2162 IBD cases and 2134 controls. Significant association was found between MIF--173G/C polymorphism and the risk of IBD when all studies were pooled into the meta-analysis (for C allele vs. G allele: OR=1.25, 95% CI=1.12-1.41, p=0.000; for C/C vs. G/G: OR=1.71, 95% CI=1.23-2.39, p=0.002; for C/C+G/C vs. G/G: OR=1.24, 95% CI=1.09-1.42, p=0.002; for C/C vs. G/C+G/G: OR=1.67, 95% CI=1.20-2.33, p=0.002). Heterogeneity and publication bias did not exist in the overall comparisons. The present meta-analysis suggests an association between the MIF--173G/C polymorphism and IBD risk. However, due to few studies and the selection bias existed in some studies, the results should be interpreted with caution.
多种流行病学研究集中于巨噬细胞移动抑制因子(MIF)基因-173G/C 多态性与炎症性肠病(IBD)之间的关联。然而,不同研究的结果并不一致。为了更精确地评估这些关联,我们进行了这项荟萃分析和对电子数据库 PubMed 和 Web of Science(截至 2013 年 4 月 30 日)的系统检索。根据我们的检索标准,共有 7 项关于 MIF-173G/C 多态性与 IBD 风险的研究符合最终荟萃分析的纳入标准,共包括 2162 例 IBD 病例和 2134 例对照。当所有研究都纳入荟萃分析时,发现 MIF-173G/C 多态性与 IBD 风险之间存在显著关联(对于 C 等位基因与 G 等位基因:OR=1.25,95%CI=1.12-1.41,p=0.000;对于 C/C 与 G/G:OR=1.71,95%CI=1.23-2.39,p=0.002;对于 C/C+G/C 与 G/G:OR=1.24,95%CI=1.09-1.42,p=0.002;对于 C/C 与 G/C+G/G:OR=1.67,95%CI=1.20-2.33,p=0.002)。总体比较中不存在异质性和发表偏倚。本荟萃分析提示 MIF-173G/C 多态性与 IBD 风险之间存在关联。然而,由于研究数量较少且部分研究存在选择偏倚,因此应谨慎解释这些结果。