Endometrial polyps: state of the problem and prediction

R. Gabidullina, G. Smirnova, A. Zaripova, E. Valeeva, T. N. Shigabutdinova, L. I. Sirmatova
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Abstract

The purpose — to study the current state of the problem of endometrial polyps, to analyze the prevalence of alleles and genotypes of the rs11841589 polymorphism of the KLF12 gene and their association with the risk of endometrial polyps and endometrial cancer in women. Material and methods. The article presents an overview of publications based on search results in the electronic resources PubMed, Elibrary, EMBASE and Google Scholar. The study included 247 women living in the Republic of Tatarstan: 86 with endometrial polyps (PE), 60 with endometrial cancer (RE), 101 patients without pathological changes in the endometrium. Clinical and laboratory examination, genotyping of the polymorphism rs11841589 of the KLF12 gene, pathomorphological examination of the endometrium were carried out. The biomaterial for genotyping the polymorphism rs11841589 of the KLF12 gene was DNA from whole blood (TestGen, Ulyanovsk). A set of reagents «Rapid-Genetics Test» by DNA-Technology LLC (Moscow, Russia) was used. The study was carried out within the framework of KSMU research No. 122082300042-2 in compliance with the principles and conditions of the Helsinki Declaration. Results. Endometrial polyps, due to their prevalence, high frequency of abnormal uterine bleeding and the risk of malignancy, represent one of the most serious gynecological problems worldwide. The mutant allele with the rs11841589 polymorphism of the KLF12 gene and the CC genotype, according to the study, do not significantly increase the risk of developing endometrial polyps and endometrial cancer in women living in the Republic of Tatarstan. It is proved that the prevalence of alleles and genotypes is comparable to the European population. Conclusion. This study showed that 247 residents of the Republic of Tatarstan included in the study had no association of rs11841589 polymorphism of the KLF12 gene with the risk of developing endometrial polyps and endometrial cancer.
子宫内膜息肉:问题的现状和预测
目的——研究子宫内膜息肉问题的现状,分析KLF12基因rs11841589多态性等位基因和基因型的流行情况及其与女性子宫内膜息肉和子宫内膜癌风险的关系。材料和方法。本文基于PubMed、library、EMBASE和b谷歌Scholar等电子资源的搜索结果对出版物进行了概述。该研究包括247名生活在鞑靼斯坦共和国的妇女:86名患有子宫内膜息肉(PE), 60名患有子宫内膜癌(RE), 101名子宫内膜无病理改变。临床和实验室检查,KLF12基因多态性rs11841589基因分型,子宫内膜病理形态学检查。KLF12基因rs11841589多态性基因分型的生物材料为全血DNA (TestGen, Ulyanovsk)。使用一套由DNA-Technology LLC (Moscow, Russia)提供的试剂“Rapid-Genetics Test”。该研究是在KSMU研究编号122082300042-2的框架内进行的,符合赫尔辛基宣言的原则和条件。结果。子宫内膜息肉因其发病率高、子宫异常出血频率高、恶性肿瘤风险大,是世界范围内最严重的妇科问题之一。根据该研究,KLF12基因rs11841589多态性的突变等位基因和CC基因型不会显著增加鞑靼斯坦共和国妇女发生子宫内膜息肉和子宫内膜癌的风险。事实证明,等位基因和基因型的流行程度与欧洲人群相当。结论。本研究发现纳入研究的247名鞑靼斯坦共和国居民KLF12基因rs11841589多态性与发生子宫内膜息肉和子宫内膜癌的风险无相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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