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本文引用的文献

1
Mitochondrial DNA copy number as a predictor of embryo viability.线粒体 DNA 拷贝数可预测胚胎活力。
Fertil Steril. 2019 Feb;111(2):205-211. doi: 10.1016/j.fertnstert.2018.11.021. Epub 2019 Jan 2.
2
Embryonal mitochondrial DNA: relationship to embryo quality and transfer outcomes.胚胎线粒体 DNA:与胚胎质量和移植结局的关系。
J Assist Reprod Genet. 2018 May;35(5):871-877. doi: 10.1007/s10815-018-1147-z. Epub 2018 Mar 5.
3
Blastulation timing is associated with differential mitochondrial content in euploid embryos.囊胚形成时间与整倍体胚胎中线粒体含量的差异有关。
J Assist Reprod Genet. 2018 Apr;35(4):711-720. doi: 10.1007/s10815-018-1113-9. Epub 2018 Jan 20.
4
Variables associated with mitochondrial copy number in human blastocysts: what can we learn from trophectoderm biopsies?人类囊胚中线粒体拷贝数的相关变量:滋养外胚层活检能告诉我们什么?
Fertil Steril. 2018 Jan;109(1):110-117. doi: 10.1016/j.fertnstert.2017.09.022.
5
Mitochondrial DNA quantity as a biomarker for blastocyst implantation potential.线粒体DNA数量作为囊胚着床潜力的生物标志物。
Fertil Steril. 2017 Nov;108(5):742-747. doi: 10.1016/j.fertnstert.2017.10.007.
6
Is mitochondrial DNA quantitation in blastocyst trophectoderm cells predictive of developmental competence and outcome in clinical IVF?囊胚滋养外胚层细胞中线粒体 DNA 定量是否可预测临床 IVF 的发育能力和结局?
J Assist Reprod Genet. 2017 Dec;34(12):1581-1585. doi: 10.1007/s10815-017-1072-6. Epub 2017 Oct 28.
7
Clinical implications of mitochondrial DNA quantification on pregnancy outcomes: a blinded prospective non-selection study.线粒体 DNA 定量分析对妊娠结局的临床意义:一项盲法前瞻性非选择研究。
Hum Reprod. 2017 Nov 1;32(11):2340-2347. doi: 10.1093/humrep/dex292.
8
Assessing the true incidence of mosaicism in preimplantation embryos.评估胚胎种植前嵌合体的真实发生率。
Fertil Steril. 2017 May;107(5):1107-1112. doi: 10.1016/j.fertnstert.2017.03.019. Epub 2017 Apr 19.
9
Mitochondrial DNA quantification as a tool for embryo viability assessment: retrospective analysis of data from single euploid blastocyst transfers.线粒体DNA定量作为评估胚胎活力的工具:对单倍体整倍体囊胚移植数据的回顾性分析
Hum Reprod. 2017 Jun 1;32(6):1282-1292. doi: 10.1093/humrep/dex070.
10
Levels of trophectoderm mitochondrial DNA do not predict the reproductive potential of sibling embryos.滋养外胚层线粒体DNA水平无法预测同胞胚胎的生殖潜力。
Hum Reprod. 2017 Apr 1;32(4):954-962. doi: 10.1093/humrep/dex034.

卵裂期线粒体 DNA 与人类胚胎发育和倍性状态相关。

Cleavage stage mitochondrial DNA is correlated with preimplantation human embryo development and ploidy status.

机构信息

IVIRMA Middle East Fertility Clinic, Abu Dhabi, United Arab Emirates.

Obstetrical Department, Women's University Hospital Tuebingen, Tübingen, Germany.

出版信息

J Assist Reprod Genet. 2019 Sep;36(9):1847-1854. doi: 10.1007/s10815-019-01520-y. Epub 2019 Jul 10.

DOI:10.1007/s10815-019-01520-y
PMID:31292817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6730730/
Abstract

PURPOSE

To evaluate whether the mitoscore of cleavage stage embryos might correlate with developmental kinetics and the ploidy status.

MATERIALS

This retrospective single-center study involved all cycles between April 2016 and April 2018 in which preimplantation genetic testing for aneuploidy (PGT-A) on day 3 was performed. The mitochondrial DNA (mtDNA) content and embryo ploidy were determined on 375 single blastomere biopsies by next generation sequencing (NGS). After intracytoplasmic sperm injection, a time-lapse imaging system (embryoscope) was used to follow the development. The median mtDNA content of cleavage stage embryos (49.4) was used to stratify the embryos into two groups to compare embryo development and ploidy status: low mitoscore group (≤ 49.4) and high mitoscore group (> 49.4).

RESULTS

The total number of euploid embryos was equal between both mitoscore groups (32.1% versus 33.5%; p = 0.854). However, embryos in the low mitoscore group had a significantly higher cell number on day 3 (8.13 ± 1.59 versus 7.62 ± 1.5; p = 0.0013) and showed a significantly faster development up until the 8-cell stage. Mitoscore was not different between euploid and aneuploid embryos, with the same blastomere number at the time of biopsy. Furthermore, absence of cavitation within 118 h after insemination was correlated with higher mitoscore values (60.22 ± 42.23 versus 50.97 ± 13.37; p = 0.006) and a lower chance of being euploid (17.1% versus 47.4%; p = 0.001).

CONCLUSION

mtDNA content of cleavage stage embryos correlates with time-lapse parameters. Early blastulation is correlated with a lower mtDNA content and a higher chance of euploidy.

摘要

目的

评估卵裂期胚胎的线粒体评分是否与发育动力学和倍性状态相关。

材料

本回顾性单中心研究纳入了 2016 年 4 月至 2018 年 4 月期间进行第三天植入前遗传学检测非整倍体(PGT-A)的所有周期。通过下一代测序(NGS)对 375 个单个卵裂球活检进行线粒体 DNA(mtDNA)含量和胚胎倍性检测。在进行胞浆内精子注射后,使用时差成像系统(胚胎镜)跟踪胚胎的发育。卵裂期胚胎的中位数 mtDNA 含量(49.4)用于将胚胎分层为两组,以比较胚胎发育和倍性状态:低线粒体评分组(≤49.4)和高线粒体评分组(>49.4)。

结果

两组的整倍体胚胎总数相同(32.1%比 33.5%;p=0.854)。然而,低线粒体评分组的胚胎在第三天的细胞数量明显更高(8.13±1.59 比 7.62±1.5;p=0.0013),并且直到 8 细胞期的发育速度明显更快。线粒体评分在整倍体和非整倍体胚胎之间没有差异,活检时的卵裂球数量相同。此外,受精后 118 小时内无囊胚腔形成与更高的线粒体评分值相关(60.22±42.23 比 50.97±13.37;p=0.006)和更低的整倍体机会(17.1%比 47.4%;p=0.001)。

结论

卵裂期胚胎的 mtDNA 含量与时差参数相关。早期卵裂与较低的 mtDNA 含量和更高的整倍体机会相关。