Jiang Yan, Tang Jun-ying, Wu Yan, Zhao Teng-fei
Department of Obstetrics and Gynecology, Chongqing Medical University, Chongqing, China.
Zhonghua Fu Chan Ke Za Zhi. 2012 Mar;47(3):179-84.
To analyze the potential association between the single nucleotide polymorphisms (SNP) of the vascular endothelial growth factor (VEGF) gene with the risk of endometriosis by meta-analysis.
Published case-control studies about the influence of VEGF polymorphisms on endometriosis were searched and screened in Medline, the Cochrane library, China National Knowledge Internet (CNKI), Chinese Biological Medicine Disk (CBM), data base of Wanfang and Foreign Medical Journal Full-Text Service (FMJS). RevMan 5.0 software was used for meta-analysis.
Finally, there were 9 literatures including 1610 endometrisis patients and 1643 controls cases, which were eligible for the criteria to investigating the VEGF SNP about -460C/T, +405C/G and +936C/T. The results of meta-analysis showed that there was no evidence for association between endometriosis and the VEGF -460C/T SNP in the genotype or allele frequencies distribution (P > 0.05). Significant differences were found between the frequencies distribution of VEGF +405CC genotype (P = 0.009, OR = 1.45, 95%CI: 1.10 - 1.91) and +405C allele (P = 0.020, OR = 1.19, 95%CI: 1.03 - 1.38), also between the +936CC genotype (P = 0.050, OR = 0.81, 95%CI: 0.66 - 1.00) and +936T allele (P = 0.040, OR = 1.20, 95%CI: 1.01 - 1.43).
The VEGF +405C/G and +936C/T SNP may be associated with the risk of endometriosis. Women carrying the +405C or the +936T allele could significantly increase the risk of developing endometriosis.
通过荟萃分析探讨血管内皮生长因子(VEGF)基因单核苷酸多态性(SNP)与子宫内膜异位症风险之间的潜在关联。
检索并筛选Medline、Cochrane图书馆、中国知网(CNKI)、中国生物医学文献数据库(CBM)、万方数据库及外文医学期刊全文数据库(FMJS)中已发表的关于VEGF基因多态性对子宫内膜异位症影响的病例对照研究。采用RevMan 5.0软件进行荟萃分析。
最终纳入9篇文献,共1610例子宫内膜异位症患者和1643例对照,符合研究VEGF基因-460C/T、+405C/G和+936C/T SNP的纳入标准。荟萃分析结果显示,在基因型或等位基因频率分布方面,子宫内膜异位症与VEGF -460C/T SNP之间无关联证据(P>0.05)。VEGF +405CC基因型(P = 0.009,OR = 1.45,95%CI:1.10 - 1.91)和+405C等位基因(P = 0.020,OR = 1.19,95%CI:1.03 - 1.38)的频率分布存在显著差异,+936CC基因型(P = 0.050,OR = 0.81,95%CI:0.66 - 1.00)和+936T等位基因(P = 0.040,OR = 1.20,95%CI:1.01 - 1.43)的频率分布也存在显著差异。
VEGF +405C/G和+936C/T SNP可能与子宫内膜异位症风险相关。携带+405C或+936T等位基因的女性患子宫内膜异位症的风险可能显著增加。