Section for Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Biomed Res Int. 2013;2013:387184. doi: 10.1155/2013/387184. Epub 2013 Aug 20.
We performed a systematic review and meta-analysis with the aim of assessing the association between cytokine gene polymorphisms and graft rejection in heart transplantation. We identified relevant studies from Medline and Embase using PubMed and Ovid search engines, respectively. Allele frequencies and allele and genotypic effects were pooled. Heterogeneity and publication bias were explored. Four to 5 studies were included in pooling of 3 gene polymorphisms. The prevalences of the minor alleles for TNF α -308, TGF β 1-c10, and TGF β 1-c25 were 0.166 (95% CI: 0.129, 0.203), 0.413 (95% CI: 0.363, 0.462), and 0.082 (95% CI: 0.054, 0.111) in the control groups, respectively. Carrying the A allele for the TNF α -308 had 18% (95% CI of OR: 0.46, 3.01) increased risk, but this was not significant for developing graft rejection than the G allele. Conversely, carrying the minor alleles for both TGF β 1-c10 and c25 had nonsignificantly lower odds of graft rejection than major alleles, with the pooled ORs of 0.87 (95% CI: 0.65, 1.18) and 0.70 (95% CI: 0.40, 1.23), respectively. There was no evidence of publication bias for all poolings. An updated meta-analysis is required when more studies are published to increase the power of detection for the association between these polymorphisms and allograft rejection.
我们进行了一项系统评价和荟萃分析,旨在评估细胞因子基因多态性与心脏移植中移植物排斥的关系。我们使用 PubMed 和 Ovid 搜索引擎分别从 Medline 和 Embase 中确定了相关研究。汇总了等位基因频率以及等位基因和基因型效应。探索了异质性和发表偏倚。有 4 到 5 项研究纳入了 3 个基因多态性的汇总分析。TNF-α-308、TGF-β1-c10 和 TGF-β1-c25 三种基因的次要等位基因在对照组中的频率分别为 0.166(95%CI:0.129,0.203)、0.413(95%CI:0.363,0.462)和 0.082(95%CI:0.054,0.111)。与 G 等位基因相比,携带 TNF-α-308 的 A 等位基因发生移植物排斥的风险增加 18%(95%CI 的 OR:0.46,3.01),但差异无统计学意义。相反,携带 TGF-β1-c10 和 c25 的次要等位基因与主要等位基因相比,发生移植物排斥的可能性较低,但差异无统计学意义,汇总的 OR 分别为 0.87(95%CI:0.65,1.18)和 0.70(95%CI:0.40,1.23)。所有汇总分析均无发表偏倚的证据。当更多的研究发表时,需要进行更新的荟萃分析,以提高这些多态性与同种异体移植排斥之间关系的检测能力。