Evaluation of Comt2, Comt3, Cyp1b1, and Esr1 gene polymorphisms as risk factor for endometrial polyp.

IF 1.2 4区 医学 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Women & Health Pub Date : 2023-11-26 Epub Date: 2023-11-17 DOI:10.1080/03630242.2023.2272206
Marcos Tcherniakovsky, Emerson de Oliveira, Marina Martinelli Sonnenfeld, Marta M Arcoverde Cavalcanti Meniconi, Marília Franco de Oliveira, Isabella Tcherniakovsky, Thomas Moscovitz, Milton Wajman, Rogers Camargo Mariano da Silva, César Eduardo Fernandes
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引用次数: 0

Abstract

The aim of this study is to evaluate COMT2, COMT3, CYP1B1, and ESR1 gene polymorphisms and occurrence of endometrial polyps. In addition, we intended to evaluate the clinical and epidemiological features of patients with and without the presence of the disease, characterizing the possible risk factors. A cross-sectional study was performed, with a total of 309 women, including 236 in the group of women with endometrial polyp confirmed by hysteroscopy and anatomical pathological examination and 73 in the group of people with diagnostic hysteroscopy without abnormal findings from the macroscopic point of view. Polymorphisms of four genes were studied: COMT2 (rs4680), COMT3 (rs5031015), CYP1B1 (rs1056836), and ESR1 (rs2234693). Polymorphism genotyping was determined using real-time polymerase chain reaction. Considering the results, no differences were identified between the two groups with respect to age, body mass index, diabetes, dyslipidemia, or smoking. The group of women without endometrial polyps showed higher use of hormone therapy than the other group (16.4 percent versus 3.8 percent, p < .001). The COMT2, COMT3, CYP1B1, and ESR1 genes exhibited no significant difference for the occurrence of endometrial polyp between the two groups. The research concluded that no correlation was identified between the genetic polymorphisms evaluated and the presence of endometrial polyps.

Comt2、Comt3、Cyp1b1和Esr1基因多态性作为子宫内膜息肉危险因素的评估。
本研究的目的是评估COMT2、COMT3、CYP1B1和ESR1基因多态性与子宫内膜息肉的发生率。此外,我们还打算评估是否存在该疾病的患者的临床和流行病学特征,以确定可能的风险因素。对309名女性进行了横断面研究,其中236名女性经宫腔镜和解剖病理检查证实患有子宫内膜息肉,73名女性经诊断性宫腔镜检查,从宏观角度没有异常发现。研究了四个基因的多态性:COMT2(rs4680)、COMT3(rs5031015)、CYP1B1(rs1056836)和ESR1(rs2234693)。利用实时聚合酶链式反应测定多态性基因分型。考虑到结果,两组在年龄、体重指数、糖尿病、血脂异常或吸烟方面没有差异。没有子宫内膜息肉的妇女组显示出比另一组更高的激素治疗使用率(16.4%对3.8%,p COMT2、COMT3、CYP1B1和ESR1基因在两组子宫内膜息肉发生率方面没有显著差异。研究得出结论,评估的遗传多态性与子宫内膜息肉的存在之间没有相关性。
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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来源期刊
Women & Health
Women & Health Multiple-
CiteScore
2.70
自引率
0.00%
发文量
73
期刊介绍: Women & Health publishes original papers and critical reviews containing highly useful information for researchers, policy planners, and all providers of health care for women. These papers cover findings from studies concerning health and illness and physical and psychological well-being of women, as well as the environmental, lifestyle and sociocultural factors that are associated with health and disease, which have implications for prevention, early detection and treatment, limitation of disability and rehabilitation.
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