探讨血浆蛋白质组与黄体存在和妊娠期及产后受孕模式的关系。

IF 2.7 3区 医学 Q2 GENETICS & HEREDITY
Dhanya Ramachandran, Robin Tarek Dewender, Bianca Schröder-Heurich, Wiebke Froböse, Florian Avdulahu, Katja Richter, Valerie L Baker, Virginia D Winn, Andreas Pich, Frauke von Versen-Höynck
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引用次数: 0

摘要

目的:观察数据表明,没有黄体的孕妇发生子痫前期的风险更高。虽然潜在的机制尚不清楚,缺乏黄体衍生的分泌产物可能是一个促成因素。本研究探讨了血浆蛋白质组在有黄体或没有黄体的妇女之间是否存在差异,并研究了与受孕方式的关系。方法:在妊娠早期、妊娠晚期和产后三个时间点采集12名参与者的血浆样本。该队列包括在不孕症后通过人工周期冷冻胚胎移植(AC FET)或自然周期冷冻胚胎移植(NC FET)受孕的妇女。使用基于质谱的蛋白质组学分析了36份血浆蛋白样本,比较了不同受孕方法和妊娠阶段有黄体和没有黄体的孕妇的蛋白质组学。结果:共检测到528个蛋白。在有和没有黄体的妇女之间没有发现差异表达的血浆蛋白。然而,15个蛋白在所有时间点在UC和FET之间表现出差异表达,bonferroni校正的p -5和FC≥bbb20 |。包括PAPPA和ANG在内的几种改变蛋白与子痫前期有关。在比较无辅助受孕方法的时间点时,SERPINA7的检测存在差异。在交流场效应管和NC场效应管之间没有发现显著差异。结论:这项初步研究揭示了与受孕模式相关的独特蛋白质组学特征。这一发现为进一步测试提供了生物学上合理的候选蛋白质。需要在更大的队列中或使用替代的蛋白质组分析技术进行验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the plasma proteome linked to corpus luteum presence and conception mode across pregnancy stages and postpartum.

Purpose: Observational data suggest that women conceiving without a corpus luteum are at higher risk of developing preeclampsia. While the underlying mechanisms remain unclear, the absence of corpus luteum-derived secretory products may be a contributing factor. This study investigates whether the plasma proteome differs between women who conceive with or without a corpus luteum and examines the relationship with mode of conception.

Methods: Plasma samples from 12 participants were collected at three time points: first trimester, third trimester, and postpartum. The cohort included women who conceived unassisted (UC) after infertility, via artificial cycle frozen embryo transfer (AC FET), or natural cycle frozen embryo transfer (NC FET). A total of 36 plasma protein samples were analyzed using mass spectrometry-based proteomics to compare the proteome of women who conceived with and without a corpus luteum, across different conception methods and pregnancy stages.

Results: In total, 528 proteins were quantified. No differentially expressed plasma proteins were identified between women with and without a corpus luteum. However, 15 proteins showed differential expression between UC and FET at all time points, with Bonferroni-corrected p < 9.47 × 10-5 and FC ≥ |2|. Several altered proteins, including PAPPA and ANG, were linked to preeclampsia. SERPINA7 was differentially detected when comparing time points within the unassisted conception method. No significant differences were detected between AC FET and NC FET.

Conclusion: This pilot study revealed a unique proteomic signature associated with the mode of conception. The findings suggest biologically plausible candidate proteins for further testing. Validation in larger cohorts or with alternative proteome analysis technologies is needed.

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来源期刊
CiteScore
5.70
自引率
9.70%
发文量
286
审稿时长
1 months
期刊介绍: The Journal of Assisted Reproduction and Genetics publishes cellular, molecular, genetic, and epigenetic discoveries advancing our understanding of the biology and underlying mechanisms from gametogenesis to offspring health. Special emphasis is placed on the practice and evolution of assisted reproduction technologies (ARTs) with reference to the diagnosis and management of diseases affecting fertility. Our goal is to educate our readership in the translation of basic and clinical discoveries made from human or relevant animal models to the safe and efficacious practice of human ARTs. The scientific rigor and ethical standards embraced by the JARG editorial team ensures a broad international base of expertise guiding the marriage of contemporary clinical research paradigms with basic science discovery. JARG publishes original papers, minireviews, case reports, and opinion pieces often combined into special topic issues that will educate clinicians and scientists with interests in the mechanisms of human development that bear on the treatment of infertility and emerging innovations in human ARTs. The guiding principles of male and female reproductive health impacting pre- and post-conceptional viability and developmental potential are emphasized within the purview of human reproductive health in current and future generations of our species. The journal is published in cooperation with the American Society for Reproductive Medicine, an organization of more than 8,000 physicians, researchers, nurses, technicians and other professionals dedicated to advancing knowledge and expertise in reproductive biology.
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