5-羟色胺转运体5-HTT基因多态性与子宫内膜异位症在意大利患者群体中缺乏相关性。

Francesca Megiorni, Serena Resta, Deliar Yazdanian, Gabriele Cavaggioni, Claudia Lia, Pierluigi Benedetti Panici, Antonio Pizzuti, Maria Grazia Porpora
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引用次数: 2

摘要

背景:本研究的目的是确定5-羟色胺转运基因(5-HTT)是否与意大利人群的子宫内膜异位症有关,5-羟色胺转运基因是控制5-羟色胺能系统的关键成分。研究结果:进行了一项病例对照研究,包括137名手术确诊的意大利子宫内膜异位症患者和120名健康对照者。聚合酶链反应和凝胶电泳分析得到5-HTT基因型(LL、SL和SS)。我们发现5-HTT基因的基因型和等位基因分布在病例和对照组之间没有总体差异。结论:我们的研究结果表明,在研究的意大利患者中,5-HTT L/S启动子多态性与子宫内膜异位症的易感性无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lack of association between serotonin transporter 5-HTT gene polymorphism and endometriosis in an Italian patient population.

Lack of association between serotonin transporter 5-HTT gene polymorphism and endometriosis in an Italian patient population.

Background: The aim of this study was to determine whether the serotonin transporter gene (5-HTT), a key component in the control of the serotonergic system, is associated with endometriosis in an Italian population.

Findings: A case-control study, comprising 137 Italian patients with surgically confirmed endometriosis and 120 healthy controls, was carried out. 5-HTT genotypes (LL, SL and SS) were obtained by polymerase chain reaction and gel electrophoresis analysis. We found no overall difference in genotypic and allelic distributions of the 5-HTT gene between cases and controls.

Conclusions: Our results suggest that the 5-HTT L/S promoter polymorphism is not associated with susceptibility to endometriosis in the studied Italian patients.

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