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The association between vascular endothelial growth factor (VEGF) +405GC genetic polymorphism and endometriosis

机译:血管内皮生长因子(VEGF)+ 405G C基因多态性与子宫内膜异位的关系

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摘要

The vascular endothelial growth factor (VEGF) is one of the most important candidate genes for the development of endometriosis, and VEGF genetic polymorphisms might be potentially associated with endometriosis risk. However, the results still remain controversial. The objective of this study aimed to perform a comprehensive meta-analysis to explore a better understanding of the effects of VEGF +405G>C genetic polymorphism on the risk of endometriosis. A total of eleven eligible studies were eventually identified in this meta-analysis, including 2829 endometriosis cases and 2947 controls. In the overall analysis, no significant association between the VEGF +405G>C genetic polymorphism and the risk of endometriosis was detected in all genetic models (for homozygote comparison [CC versus vs. GG]: OR = 1.21, 95% CI 0.67–2.19, P = 0.537; for heterozygote comparison [CG vs. GG]: OR = 1.16, 95% CI 0.86–1.56, P = 0.348; for dominant comparison CC/CG vs. GG: OR = 1.10, 95% CI 0.93–1.30, P = 0.263; for recessive comparison [CC vs. CG/GG]: OR = 1.03, 95% CI 0.73–1.47, P = 0.857; allele comparison [C vs. G]: OR = 0.99, 95% CI 0.70–1.40, P = 0.962). In the subgroup analysis by ethnicities, there was no significant association between VEGF +405G>C genetic polymorphism and endometriosis risk in Asians and/or Caucasians under all genetic models (all P-values >0.05). No publication bias was observed in this study. This meta-analysis supports that the VEGF +405G>C genetic polymorphism is not significant associated with the risk of endometriosis.
机译:血管内皮生长因子(VEGF)是子宫内膜异位症发展的最重要候选基因之一,而VEGF基因多态性可能与子宫内膜异位症的风险相关。但是,结果仍然存在争议。本研究的目的是进行全面的荟萃分析,以更好地了解VEGF + 405G> C基因多态性对子宫内膜异位症风险的影响。该荟萃分析最终鉴定出总共11项合格研究,包括2829例子宫内膜异位病例和2947例对照。在总体分析中,在所有遗传模型中均未发现VEGF + 405G> C基因多态性与子宫内膜异位症风险之间存在显着关联(对于纯合子比较[CC vs. GG]:OR = 1.21,95%CI 0.67-2.19) ,P = 0.537;对于杂合子比较[CG与GG]:OR = 1.16,95%CI 0.86-1.56,P = 0.348;对于显性比较CC / CG与GG:OR = 1.10,95%CI 0.93-1.30 ,P = 0.263;对于隐性比较[CC vs. CG / GG]:OR = 1.03,95%CI 0.73-1.47,P = 0.857;等位基因比较[C vs. G]:OR = 0.99,95%CI 0.70- 1.40,P = 0.962)。在按种族进行的亚组分析中,在所有遗传模型下,亚洲人和/或高加索人中VEGF + 405G> C基因多态性与子宫内膜异位症风险之间均无显着关联(所有P值> 0.05)。在这项研究中没有观察到发表偏见。该荟萃分析支持VEGF + 405G> C基因多态性与子宫内膜异位症的风险无关。

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