人颗粒细胞B细胞易位基因2表达水平与体外受精/胞浆内单精子注射结果负相关:一项初步研究

IF 3.2 3区 医学 Q2 GENETICS & HEREDITY
Jiahuan Luo, Huawei Wang, Ling Zhou, Longda Wang, Jinyuan Wang, Mengjie Song, Yulin Cheng, Meng Rao, Shuhua Zhao, Li Tang
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引用次数: 0

摘要

目的:本研究旨在监测b细胞易位基因2 (BTG2)在体外受精/ICSI患者颗粒细胞中的表达与囊胚质量的关系。方法:我们招募了181名接受IVF/ICSI周期治疗不孕症的妇女。从卵泡液中提取颗粒细胞。将颗粒细胞BTG2表达水平分为低、中、高三分位,采用Kruskal-Wallis分析比较各分位患者的预后指标。采用Spearman相关分析评价BTG2 mRNA水平与预后指标的相关性。采用平滑样条的广义线性模型和广义加性模型来调整潜在的混杂因素。结果:低BTG2胚芽的患者比高BTG2胚芽的患者有更高的卵母细胞回收、受精、囊胚形成和高质量囊胚率。BTG2高胚芽位患者的着床率和临床妊娠率较BTG2低胚芽位或中等胚芽位患者呈下降趋势,而早期妊娠损失率呈上升趋势,但差异不显著。在调整混杂因素后,BTG2的表达水平与卵母细胞回收、囊胚形成和高质量囊胚率呈负相关。AMH bbb40ng /ml的分层分析显示,BTG2表达升高与卵母细胞回收、受精、卵裂、囊胚形成和高质量囊胚率降低有关。在AMH≤4 ng/ml的患者中,这些结果没有差异。结论:在AMH水平高(bbb40 ng/ml)的女性中,颗粒细胞中BTG2表达升高与囊胚质量差有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
B cell translocation gene 2 expression levels in human granulosa cells is negatively associated with in vitro fertilization/intracytoplasmic sperm injection outcomes: a pilot study.

Purpose: This study aimed to monitor the expression of B-cell translocation gene 2 (BTG2) in granulosa cells of patients undergoing IVF/ICSI with respect blastocyst quality outcomes.

Methods: We recruited 181 women undergoing IVF/ICSI cycles for infertility. Granulosa cells were extracted from follicular fluid. BTG2 expression level of granulosa cells were stratified into tertiles (low, middle, and high), and the patients of each tertile were compared for outcome indicators by Kruskal-Wallis analysis. Spearman's correlation analyses were used to evaluate the correlation between BTG2 mRNA levels and outcome indicators. Generalized linear models and generalized additive models with smoothing splines were used to adjust for potential confounders.

Results: Patients in the low BTG2 tertile had higher oocyte retrieval, fertilization, blastocyst formation, and high-quality blastocyst rates than those in the high BTG2 tertile. Patients in the high BTG2 tertile exhibited a downward trend in implantation and clinical pregnancy rates compared to those in the low or middle BTG2 tertiles, whereas the early pregnancy loss rate showed an upward trend, although the difference was not significant. After adjusting for confounding factors, the expression level of BTG2 was negatively correlated with oocyte retrieval, blastocyst formation, and high-quality blastocyst rates. Stratified analysis of AMH > 4 ng/ml showed elevated BTG2 expression was associated with reduced oocyte retrieval, fertilization, cleavage, blastocyst formation, and high-quality blastocyst rates. No differences in these outcomes were observed in patients with AMH ≤ 4 ng/ml.

Conclusion: In women with high AMH levels (> 4 ng/ml) elevated BTG2 expression in granulosa cells was associated with poor quality blastocyst outcomes.

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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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