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本文引用的文献

1
Cumulus and granulosa cell markers of oocyte and embryo quality.卵母细胞和胚胎质量的卵丘细胞和颗粒细胞标志物。
Fertil Steril. 2013 Mar 15;99(4):979-97. doi: 10.1016/j.fertnstert.2013.01.129.
2
Embryo incubation and selection in a time-lapse monitoring system improves pregnancy outcome compared with a standard incubator: a retrospective cohort study.在延时监测系统中进行胚胎孵育和选择可改善妊娠结局,优于标准孵育器:一项回顾性队列研究。
Fertil Steril. 2012 Dec;98(6):1481-9.e10. doi: 10.1016/j.fertnstert.2012.08.016. Epub 2012 Sep 10.
3
Day 3 embryo selection by metabolomic profiling of culture medium with near-infrared spectroscopy as an adjunct to morphology: a randomized controlled trial.第 3 天胚胎选择:利用近红外光谱对培养基进行代谢组学分析,作为形态学的辅助手段:一项随机对照试验。
Hum Reprod. 2012 Aug;27(8):2304-11. doi: 10.1093/humrep/des175. Epub 2012 May 30.
4
Embryonic poly(A)-binding protein (EPAB) is required for oocyte maturation and female fertility in mice.胚胎多聚腺苷酸结合蛋白 (EPAB) 对于小鼠卵母细胞成熟和雌性生育力是必需的。
Biochem J. 2012 Aug 15;446(1):47-58. doi: 10.1042/BJ20120467.
5
Embryo assessment strategies and their validation for clinical use: a critical analysis of methodology.胚胎评估策略及其临床验证的方法学分析。
Curr Opin Obstet Gynecol. 2012 Jun;24(3):141-50. doi: 10.1097/GCO.0b013e328352cd17.
6
Non-invasive metabolomic profiling of Day 2 and 5 embryo culture medium: a prospective randomized trial.第 2 天和第 5 天胚胎培养液的非侵入性代谢组学分析:一项前瞻性随机试验。
Hum Reprod. 2012 Jan;27(1):89-96. doi: 10.1093/humrep/der373. Epub 2011 Nov 7.
7
LC-MS-based metabolomics.基于液相色谱-质谱联用的代谢组学
Mol Biosyst. 2012 Feb;8(2):470-81. doi: 10.1039/c1mb05350g. Epub 2011 Nov 1.
8
Live birth outcome with trophectoderm biopsy, blastocyst vitrification, and single-nucleotide polymorphism microarray-based comprehensive chromosome screening in infertile patients.在不孕患者中,通过滋养层活检、囊胚玻璃化和基于单核苷酸多态性微阵列的全面染色体筛查获得活产结局。
Fertil Steril. 2011 Sep;96(3):638-40. doi: 10.1016/j.fertnstert.2011.06.049. Epub 2011 Jul 23.
9
Genome-wide analysis of translation reveals a critical role for deleted in azoospermia-like (Dazl) at the oocyte-to-zygote transition.全基因组翻译分析揭示了缺失于无精子症样(DAZL)在卵母细胞到合子过渡中的关键作用。
Genes Dev. 2011 Apr 1;25(7):755-66. doi: 10.1101/gad.2028911.
10
Cross-validation and predictive value of near-infrared spectroscopy algorithms for day-5 blastocyst transfer.第5天囊胚移植的近红外光谱算法的交叉验证和预测价值。
Reprod Biomed Online. 2011 May;22(5):477-84. doi: 10.1016/j.rbmo.2011.01.009. Epub 2011 Jan 24.

胚胎活力的代谢组学评估。

Metabolomic assessment of embryo viability.

作者信息

Uyar Asli, Seli Emre

机构信息

Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, Connecticut.

出版信息

Semin Reprod Med. 2014 Mar;32(2):141-52. doi: 10.1055/s-0033-1363556. Epub 2014 Feb 10.

DOI:10.1055/s-0033-1363556
PMID:24515909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4109799/
Abstract

Preimplantation embryo metabolism demonstrates distinctive characteristics associated with the developmental potential of embryos. On this basis, metabolite content of culture media was hypothesized to reflect the implantation potential of individual embryos. This hypothesis was tested in consecutive studies reporting a significant association between culture media metabolites and embryo development or clinical pregnancy. The need for a noninvasive, reliable, and rapid embryo assessment strategy promoted metabolomics studies in vitro fertilization (IVF) in an effort to increase success rates of single embryo transfers. With the advance of analytical techniques and bioinformatics, commercial instruments were developed to predict embryo viability using spectroscopic analysis of surplus culture media. However, despite the initial promising results from proof-of-principal studies, recent randomized controlled trials using commercial instruments failed to show a consistent benefit in improving pregnancy rates when metabolomics is used as an adjunct to morphology. At present, the application of metabolomics technology in clinical IVF laboratory requires the elimination of factors underlying inconsistent findings, when possible, and development of reliable predictive models accounting for all possible sources of bias throughout the embryo selection process.

摘要

植入前胚胎代谢表现出与胚胎发育潜能相关的独特特征。在此基础上,有人推测培养基中的代谢物含量可反映单个胚胎的着床潜能。在一系列研究中对这一假设进行了验证,这些研究报告了培养基代谢物与胚胎发育或临床妊娠之间存在显著关联。对无创、可靠且快速的胚胎评估策略的需求推动了体外受精(IVF)代谢组学研究,以提高单胚胎移植的成功率。随着分析技术和生物信息学的发展,开发了商业仪器,通过对多余培养基进行光谱分析来预测胚胎活力。然而,尽管初步的原理验证研究取得了令人鼓舞的结果,但最近使用商业仪器的随机对照试验表明,当代谢组学作为形态学的辅助手段时,在提高妊娠率方面未能显示出一致的益处。目前,代谢组学技术在临床IVF实验室中的应用需要尽可能消除导致结果不一致的因素,并开发可靠的预测模型,以考虑胚胎选择过程中所有可能的偏差来源。