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The Association Analysis of Vascular Endothelial Growth Factor -2549 Insertion/ Deletion Variant and Endometriosis Risk

机译:血管内皮生长因子-2549插入/缺失变异与子宫内膜异位风险的关联分析

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摘要

Endometriosis is a debilitating disorder, defined as the presence of endometrial gland and stroma outside of the uterus. It may affect angiogenesis and is one of the angiogenic factors that plays an important role in both physiological and pathological angiogenesis. The present study aimed to evaluate the association of -2549 insertion/deletion (I/D) polymorphism with endometriosis. This case-control study enrolled 244 (100 cases and 144 controls) women who were admitted for laparoscopy or laparotomy for gynecological procedures. Genomic DNA was separated from peripheral blood leukocytes and polymerase chain reaction (PCR) amplification was performed for genotyping of the gene Insertion/Deletion (I/D) polymorphism. The frequency of the II, ID, and DD genotype was 14%, 52% and 34% in patients versus 18.8%, 47.8% and 34% in controls. The results did not provide any evidence supporting the endometriosis risk related to the polymorphism in a group of Iranian women population.
机译:子宫内膜异位症是一种使人衰弱的疾病,定义为子宫外存在子宫内膜腺体和间质。它可能影响血管生成,并且是在生理和病理性血管生成中都起重要作用的血管生成因子之一。本研究旨在评估-2549插入/缺失(I / D)多态性与子宫内膜异位的关联。这项病例对照研究招募了244例(100例病例和144例对照)女性,这些女性因妇科手术而接受了腹腔镜或剖腹手术。从外周血白细胞中分离基因组DNA,并进行聚合酶链反应(PCR)扩增,以进行基因插入/缺失(I / D)多态性的基因分型。 II,ID和DD基因型的频率在患者中分别为14%,52%和34%,而在对照组中分别为18.8%,47.8%和34%。结果没有提供任何证据支持与一群伊朗女性人群多态性有关的子宫内膜异位症风险。

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