Supporting the One-Carbon Cycle Restores Ovarian Reserve in Subfertile Women: Absence of Correlation with Urinary Bisphenol A Concentration.

Q2 Biochemistry, Genetics and Molecular Biology
BioResearch Open Access Pub Date : 2017-08-01 eCollection Date: 2017-01-01 DOI:10.1089/biores.2017.0016
Erica Silvestris, Marc Cohen, Dominique Cornet, Laetitia Jacquesson-Fournols, Patrice Clement, Jacques Chouteau, Marc Schneider, Thierry Besnard, Yves Ménézo
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引用次数: 13

Abstract

Environmental endocrine disrupting chemicals (EDCs), including bisphenol A (BPA), induce DNA methylation errors and oxidative stress, and alter fertility. Animal studies have demonstrated that supporting the one-carbon cycle (1-CC) with appropriate dietary supplements can reduce the effects of EDCs. Anti-Mullerian hormone (AMH), a marker of ovarian functionality, has been tested in subfertile female patients, to control this hypothesis in humans. Fifty-five women with a history of 3-7 years of infertility, with at least two assisted reproductive technology (ART) treatment failures, and low serum levels of AMH were enrolled in the study. Before starting any further ART treatment, they were tested for AMH and for follicular count. A urinary control of BPA was proposed. Then a support of the 1-CC, already tested in other clinical studies, was initiated and continued for 4 months. At the end of this period, antral follicle count and serum AMH levels were re-evaluated. The AMH levels before and after treatment were compared using the Wilcoxon test (nonparametric test, non-Gaussian population). Out of the 55 patients, 35 accepted a BPA dosage in the urine. No correlation was found between BPA and serum AMH concentrations. Forty-nine patients followed the full treatment with 1-CC supplements, which resulted in increased AMH levels, independent of initial AMH levels and maternal age (in the range studied), p = 0.0001. Eight patients spontaneously conceived ongoing pregnancies within 3 months, at the end of the protocol. A support of the 1-CC can partly alleviate metabolic derangements induced by environment, as observed in animal models, and improve endocrine background in women.

Abstract Image

Abstract Image

支持单碳循环恢复低生育能力妇女卵巢储备:与尿双酚A浓度无相关性。
环境内分泌干扰化学物质(EDCs),包括双酚A (BPA),诱导DNA甲基化错误和氧化应激,并改变生育能力。动物研究表明,通过适当的膳食补充剂支持一碳循环(1-CC)可以减少EDCs的影响。抗苗勒管激素(AMH)是卵巢功能的标志,已经在不孕女性患者中进行了测试,以控制人类的这种假设。55名有3-7年不孕症史、至少两次辅助生殖技术(ART)治疗失败、血清AMH水平低的妇女参加了这项研究。在开始任何进一步的抗逆转录病毒治疗之前,他们进行了AMH和卵泡计数检测。提出了尿中BPA的控制方法。然后,已经在其他临床研究中测试过的1-CC的支持开始并持续了4个月。在这段时间结束时,重新评估窦卵泡计数和血清AMH水平。治疗前后AMH水平比较采用Wilcoxon检验(非参数检验,非高斯总体)。在55名患者中,35人接受了尿液中BPA剂量的检测。BPA与血清AMH浓度无相关性。49名患者接受了1-CC补充剂的全面治疗,这导致AMH水平升高,与初始AMH水平和母亲年龄无关(在研究范围内),p = 0.0001。在试验结束时,8名患者在3个月内自然怀孕。在动物模型中观察到,1-CC的支持可以部分缓解环境引起的代谢紊乱,并改善女性的内分泌背景。
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来源期刊
BioResearch Open Access
BioResearch Open Access Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
自引率
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1
期刊介绍: BioResearch Open Access is a high-quality open access journal providing peer-reviewed research on a broad range of scientific topics, including molecular and cellular biology, tissue engineering, regenerative medicine, stem cells, gene therapy, systems biology, genetics, virology, and neuroscience. The Journal publishes basic science and translational research in the form of original research articles, comprehensive review articles, mini-reviews, rapid communications, brief reports, technology reports, hypothesis articles, perspectives, and letters to the editor.
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