Gholamreza Niaei, S. Heidaryan, A. Niaei, Nasim Alsadat Didevar
{"title":"Association between Vascular Endothelial Growth Factor (VEGF) -1154G/A Polymorphism and Endometriosis in North West of Iran","authors":"Gholamreza Niaei, S. Heidaryan, A. Niaei, Nasim Alsadat Didevar","doi":"10.22037/JPS.V8I4.16793","DOIUrl":null,"url":null,"abstract":"Endometriosis is considered as a multifactorial disease that affects up to 10% of all women of fertile age. Vascular endothelial growth factor (VEGF) is one of the most important activators of angiogenesis. VEGF is known to be a key molecule in the pathogenesis of endometriosis. A great number of studies have referred to genetic polymorphisms as a factor that contributes to the development of endometriosis. The present study was aimed to find out the frequency of the VEGF -1154G/A polymorphism and its relationship with endometriosis risk in Iranian women with endometriosis.This study involved 175 patients with endometriosis and 131 healthy controls. Following extraction of genomic DNA from patients and controls, genotyping of the -1154G/A polymorphism of the VEGF gene were performed by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis. Multivariate analysis was used to examine the association between the risk of endometriosis and VEGF -1154G/A polymorphism. There was statistically a significant difference in the frequency of the -1154G/A polymorphism between patients and the controls. The percentage distribution of the three -1154G/A genotypes was (GG 3.4%, GA %46.8%, AA 49.7%) in endometriosis patients. Conclusion : Data supports the hypothesis that angiogenesis is of pivotal importance in the development of endometriosis. Our study indicates that there is significant association between the VEGF gene -1154G/A polymorphism and the risk of endometriosis in North West of Iran.","PeriodicalId":16663,"journal":{"name":"Journal of paramedical sciences","volume":"75 1 1","pages":"21-25"},"PeriodicalIF":0.0000,"publicationDate":"2017-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of paramedical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22037/JPS.V8I4.16793","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Endometriosis is considered as a multifactorial disease that affects up to 10% of all women of fertile age. Vascular endothelial growth factor (VEGF) is one of the most important activators of angiogenesis. VEGF is known to be a key molecule in the pathogenesis of endometriosis. A great number of studies have referred to genetic polymorphisms as a factor that contributes to the development of endometriosis. The present study was aimed to find out the frequency of the VEGF -1154G/A polymorphism and its relationship with endometriosis risk in Iranian women with endometriosis.This study involved 175 patients with endometriosis and 131 healthy controls. Following extraction of genomic DNA from patients and controls, genotyping of the -1154G/A polymorphism of the VEGF gene were performed by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis. Multivariate analysis was used to examine the association between the risk of endometriosis and VEGF -1154G/A polymorphism. There was statistically a significant difference in the frequency of the -1154G/A polymorphism between patients and the controls. The percentage distribution of the three -1154G/A genotypes was (GG 3.4%, GA %46.8%, AA 49.7%) in endometriosis patients. Conclusion : Data supports the hypothesis that angiogenesis is of pivotal importance in the development of endometriosis. Our study indicates that there is significant association between the VEGF gene -1154G/A polymorphism and the risk of endometriosis in North West of Iran.
子宫内膜异位症被认为是一种多因素疾病,影响多达10%的育龄妇女。血管内皮生长因子(VEGF)是血管生成的重要激活因子之一。已知VEGF是子宫内膜异位症发病的关键分子。大量的研究已经提到遗传多态性是导致子宫内膜异位症发展的一个因素。本研究旨在了解伊朗子宫内膜异位症女性中VEGF -1154G/A多态性的频率及其与子宫内膜异位症风险的关系。这项研究涉及175名子宫内膜异位症患者和131名健康对照者。提取患者和对照组基因组DNA后,采用聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析对VEGF基因-1154G/A多态性进行基因分型。采用多因素分析来研究子宫内膜异位症风险与VEGF -1154G/A多态性之间的关系。患者与对照组-1154G/ a多态性发生频率差异有统计学意义。3种-1154G/A基因型在子宫内膜异位症患者中的百分比分布为(GG 3.4%, GA 46.8%, AA 49.7%)。结论:数据支持血管生成在子宫内膜异位症的发展中起关键作用的假设。我们的研究表明,在伊朗西北部地区,VEGF基因-1154G/A多态性与子宫内膜异位症的风险存在显著相关性。