Department of Emergency, Chinese PLA Air Force General Hospital, Haidian District, Beijing, China.
J Surg Res. 2012 Nov;178(1):409-14. doi: 10.1016/j.jss.2012.02.001. Epub 2012 Apr 2.
Epidemiologic studies have evaluated the association between tumor necrosis factor-alpha (TNF-α) gene -308A/G polymorphism and the risk of acute pancreatitis (AP), but the results are inconsistent. In order to derive a more precise estimation of the associations, a meta-analysis was performed.
Systematic searches of electronic databases PubMed, Embase, and Web of Science, as well as hand searching of the references of identified articles, were performed. All case-control studies investigating the association between TNF-α gene -308A/G polymorphism and AP risk were included. The association was assessed by odds ratio (OR) with 95% confidence intervals (CIs). Publication bias was analyzed by Begg's funnel plot and Egger's regression test.
The initial search revealed 818 potentially eligible studies. Having read the title, abstract, or full text, we included six relevant studies in the final meta-analysis, which contained 1,006 AP cases and 782 controls. Overall, no significant association was found between TNF-α gene -308A/G polymorphism and AP risk when all studies were pooled into the meta-analysis (for A/A+A/G versus G/G: OR = 1.03, 95% CI = 0.83-1.28, P = 0.79; for A/A versus A/G+G/G: OR = 0.97, 95% CI = 0.65-1.45, P = 0.87; for A/A versus G/G: OR = 1.23, 95% CI = 0.79-1.91, P = 0.37; for A allele versus G allele: OR = 0.99, 95% CI = 0.83-1.18, P = 0.90). In addition, the similar results were obtained in the subgroup analysis based on the ethnicity and subtype of AP.
The present meta-analysis reveals that the TNF-α gene -308A/G polymorphism is not associated with AP risk. However, due to the small number of subjects included in analysis and the selection bias in some studies, the results should be interpreted with caution.
流行病学研究已经评估了肿瘤坏死因子-α(TNF-α)基因 -308A/G 多态性与急性胰腺炎(AP)风险之间的关联,但结果不一致。为了更准确地评估这些关联,进行了荟萃分析。
对电子数据库 PubMed、Embase 和 Web of Science 进行系统搜索,并对已确定文章的参考文献进行手工搜索。 所有研究 TNF-α基因-308A/G 多态性与 AP 风险之间关联的病例对照研究均包括在内。 关联通过优势比(OR)和 95%置信区间(CI)进行评估。 通过 Begg 漏斗图和 Egger 回归检验分析发表偏倚。
最初的搜索显示出 818 项潜在的合格研究。 在阅读标题、摘要或全文后,我们将最终荟萃分析中包含的六项相关研究纳入其中,其中包含 1006 例 AP 病例和 782 例对照。 总体而言,当所有研究都纳入荟萃分析时,TNF-α基因-308A/G 多态性与 AP 风险之间没有显著关联(对于 A/A+A/G 与 G/G:OR=1.03,95%CI=0.83-1.28,P=0.79;对于 A/A 与 A/G+G/G:OR=0.97,95%CI=0.65-1.45,P=0.87;对于 A/A 与 G/G:OR=1.23,95%CI=0.79-1.91,P=0.37;对于 A 等位基因与 G 等位基因:OR=0.99,95%CI=0.83-1.18,P=0.90)。 此外,基于 AP 的种族和亚型的亚组分析也得到了相似的结果。
本荟萃分析表明,TNF-α基因-308A/G 多态性与 AP 风险无关。 然而,由于分析中纳入的受试者数量较少以及一些研究中的选择偏倚,结果应谨慎解释。