RANKL是绝经期血管舒缩症状的一种新的表观遗传生物标志物。

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY Balkan Journal of Medical Genetics Pub Date : 2020-08-26 eCollection Date: 2020-06-01 DOI:10.2478/bjmg-2020-0001
R Kalkan, M Altarda, O Tosun
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引用次数: 3

摘要

在绝经过渡期,雌激素水平的下降带来了许多生理问题和激素的变化。在这项研究中,使用甲基化特异性高分辨率融化(MS-HRM)分析,在30名绝经前和35名绝经后妇女中鉴定了RANKL和FSHR基因的启动子甲基化。16例绝经后患者检测到RANKL基因,12例(75.0%)RANKL甲基化患者出现潮热(p = 0.024),采用Pearson χ2和Fisher精确检验进行统计学分析及其与患者特征的相关性。18例绝经后患者中检测到FSHR基因甲基化,其中13例(75.0%)出现潮热(p = 0.028)。体外研究证实了RANKL表达、FSH水平与小鼠潮热之间的关联。虽然缺乏这一领域的表观遗传学研究证明了我们的结果至关重要,因此,我们的结果显示了土族塞人绝经后妇女的表观遗传学概况。这是第一个研究RANKL和FSHR甲基化及其与绝经后妇女潮热关系的研究。
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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RANKL is a new Epigenetic Biomarker for the Vasomotor Symptom During Menopause.

During menopausal transition, decreased level of estrogen brings a number of physiological problems and hormonal changes. In this study, promoter methylation of RANKL and FSHR genes were identified in 30 premenopausal and 35 postmenopausal women using methylation-specific high resolution melting (MS-HRM) analysis. The statistical analyses and their association with patient characteristics were performed by Pearson χ2 and Fisher's exact test (p <0.05). The methylated RANKL gene was detected in 16 postmenopausal cases, and 12 (75.0%) of the RANKL methylated cases had hot flashes (p = 0.024). The methylated FSHR gene was detected in 18 postmenopausal cases, and 13 (75.0%) of the methylated cases had hot flashes (p = 0.028). In vitro studies demonstrated the association between RANKL expression, FSH level and hot flashes in the mouse. Although lack of epigenetic studies in this field proves our results crucial and therefore, our results showed magnitude of epigenetic profiles of Turkish Cypriot post-menopausal women. This was the first study which has investigated the RANKL and FSHR methylation and their relationship with hot flashes in postmenopausal women.

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来源期刊
CiteScore
1.00
自引率
0.00%
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审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
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