State Key Laboratory of Cancer Biology, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an 710032, Shannxi, China.
J Gastroenterol. 2011 Oct;46(10):1158-66. doi: 10.1007/s00535-011-0441-7. Epub 2011 Jul 30.
Recent studies proved that inflammatory bowel disease (IBD) patients had a higher risk of thromboembolism and a Factor V Leiden mutation that prevents the efficient inactivation of factor V, which leads to thromboembolism and thus contributes to a high potential risk of IBD. However, the relationship between Factor V Leiden mutation and IBD remains controversial.
We conducted a systematic review with meta-analysis of studies assessing the association of Factor V Leiden mutation with the risk of IBD in humans. We extracted the number of IBD and control subjects with or without Factor V Leiden mutation from each study and conducted this analysis using a fixed-effects model.
Nineteen studies met the inclusion criteria and were included in the meta-analysis. No significant heterogeneity was found in results across the 19 studies (I (2) = 18.8%, P = 0.23), which showed a slight but not significant increase in the risk of IBD with Factor V Leiden mutation in the general population (summary odds ratio [OR] 1.13, 95% confidence interval [CI] 0.87-1.46). Taking into account ethnic differences, further study exhibited a slight but not significant increase in risk of IBD with Factor V Leiden mutation in Europeans (summary OR 1.20, 95% CI 0.88-1.64). However, Factor V Leiden mutation was significantly associated with a higher risk of thromboembolism in IBD patients (summary OR 5.30, 95% CI 2.25-12.48). No publication bias was found in this study.
This meta-analysis indicated that although Factor V Leiden mutation was not significantly associated with the risk of IBD, it was significantly associated with a higher risk of thromboembolism in IBD patients.
最近的研究证明,炎症性肠病(IBD)患者发生血栓栓塞的风险较高,且存在一种因子 V 莱顿突变,可阻止因子 V 有效失活,从而导致血栓栓塞,并因此增加 IBD 的高潜在风险。然而,因子 V 莱顿突变与 IBD 之间的关系仍存在争议。
我们对评估因子 V 莱顿突变与人类 IBD 风险之间关联的研究进行了系统评价和荟萃分析。我们从每项研究中提取了具有或不具有因子 V 莱顿突变的 IBD 和对照受试者的数量,并使用固定效应模型进行了此分析。
19 项研究符合纳入标准并被纳入荟萃分析。19 项研究的结果无显著异质性(I²=18.8%,P=0.23),表明一般人群中因子 V 莱顿突变略微但无统计学意义地增加了 IBD 的风险(汇总优势比[OR]1.13,95%置信区间[CI]0.87-1.46)。考虑到种族差异,进一步的研究表明,欧洲人群中因子 V 莱顿突变与 IBD 的风险略有但无统计学意义地增加(汇总 OR 1.20,95%CI0.88-1.64)。然而,因子 V 莱顿突变与 IBD 患者血栓栓塞的风险显著相关(汇总 OR 5.30,95%CI2.25-12.48)。本研究未发现发表偏倚。
本荟萃分析表明,尽管因子 V 莱顿突变与 IBD 的风险无显著相关性,但与 IBD 患者血栓栓塞的风险显著相关。