Eldafira Eldafira, Prasasty Vivitri Dewi, Abinawanto Abinawanto, Syahfirdi Luthfiralda, Pujianto Dwi Ari
Universitas Indonesia, Faculty of Medicine, Department of Medical Biology, Depok, Indonesia.
Universitas Indonesia, Faculty of Mathematics and Natural Sciences, Department of Biology, Jakarta, Indonesia.
Turk J Pharm Sci. 2021 Feb 25;18(1):91-95. doi: 10.4274/tjps.galenos.2019.94914.
Endometriosis is a common gynecological disorder, characterized by the presence of endometrial-like tissue in the extrauterine location. The increasing estradiol concentration can influence endometriosis risk and estrogen receptor (ER) activity. Polymorphism in ER causes gene expression alteration and influences hormone-receptor interaction. This research aims to determine ER genetic polymorphisms in endometriosis pathogenesis.
This study was performed on case-control polymorphisms, which compared 83 women with endometriosis and 76 women without endometriosis. However, the samples used for gene expression analysis and estrogen level measurement were obtained from 18 women with endometriosis and 18 women without endometriosis. Polymerase chain reaction-restriction fragment length polymorphism was used to determine ER genetic polymorphisms. Chi-square, Mann-Whitney test, Spearman's correlation (p), t-independent, and two-tailed tests were used to analyze the data.
Association between the allele ERα rs9340799 A/G and endometriosis was significantly different (p=0.012), whereas rs2234693 T/C polymorphism showed no association with endometriosis. The correlation between the genotype frequencies of allele ERβ rs4986938 G/A and endometriosis was found significantly different (p=0.015; p=0.034).
Estradiol level and ERβ expression increases, polymorphism genotypes and alleles of gene and allele frequency of gene have roles in endometriosis.
子宫内膜异位症是一种常见的妇科疾病,其特征是子宫外出现类似子宫内膜的组织。雌二醇浓度的升高会影响子宫内膜异位症的风险和雌激素受体(ER)活性。ER基因多态性会导致基因表达改变,并影响激素-受体相互作用。本研究旨在确定ER基因多态性在子宫内膜异位症发病机制中的作用。
本研究采用病例对照多态性研究,比较了83例子宫内膜异位症患者和76例非子宫内膜异位症患者。然而,用于基因表达分析和雌激素水平测量的样本来自18例子宫内膜异位症患者和18例非子宫内膜异位症患者。采用聚合酶链反应-限制性片段长度多态性方法来确定ER基因多态性。使用卡方检验、曼-惠特尼检验、斯皮尔曼相关性(p)、独立t检验和双尾检验来分析数据。
等位基因ERα rs9340799 A/G与子宫内膜异位症之间的关联存在显著差异(p = 0.012),而rs2234693 T/C多态性与子宫内膜异位症无关联。发现等位基因ERβ rs4986938 G/A的基因型频率与子宫内膜异位症之间的相关性存在显著差异(p = 0.015;p = 0.034)。
雌二醇水平和ERβ表达增加,基因的多态性基因型和等位基因以及基因的等位基因频率在子宫内膜异位症中起作用。