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玻璃化冷冻保存卵裂期胚胎可能会影响胚胎植入前遗传学检测的胚胎发育潜能。

Accumulation of Cleavage-Stage Embryos by Vitrification may Compromise Embryonic Developmental Potential in Preimplantation Genetic Testing.

机构信息

Chongqing Health Center for Women and Children, Chongqing, People's Republic of China.

Chongqing Key Laboratory of Human Embryo Engineering, Chongqing, People's Republic of China.

出版信息

Reprod Sci. 2022 Jun;29(6):1930-1938. doi: 10.1007/s43032-022-00880-8. Epub 2022 Feb 25.

DOI:10.1007/s43032-022-00880-8
PMID:35212931
Abstract

It was suggested that the embryo pooling was an alternative for patients with insufficient number of embryos for preimplantation genetic testing (PGT) in a single ovarian stimulation cycle. However, limited study noticed whether it is an efficient strategy to pool cleavage-stage embryos by vitrification. This study included 71 cycles with vitrified-warmed and fresh embryos simultaneously for PGT between May 2016 and May 2021. The embryos from the same patients were split into two groups based on the origin: warming group and fresh group. Embryo development, sequencing results, clinical and neonatal outcomes were compared. The results showed that the rate of high-quality embryos in the warming group was significantly higher than that in the fresh group (64.53% versus 52.61%, P = 0.011); however, the available blastocyst rate in this group was significantly lower than that in the fresh group (47.29% versus 57.83%, P = 0.026). There were 96 and 144 blastocysts that underwent trophectoderm (TE) biopsy in warming and fresh groups, respectively. The high-quality blastocyst rate was significantly lower in the warming group compared to the fresh group (57.29% versus 70.14%, P = 0.041). The rates of genetic transferable blastocyst were comparable between the two groups (P = 0.956). There were no statistical differences in terms of embryo implantation, clinical pregnancy, miscarriage rates, and neonatal outcomes between the two groups. In conclusion, this study demonstrated that the cleavage-stage embryo pooling strategy might be unfavorable for the maintenance of embryonic development potential. If not necessary, it is not recommended to pool cleavage-stage embryos for PGT.

摘要

有人提出,在单个卵巢刺激周期中,对于胚胎数量不足进行胚胎植入前遗传学检测(PGT)的患者,胚胎pooling 是一种替代方案。然而,有限的研究注意到通过玻璃化冷冻来pooling 卵裂期胚胎是否是一种有效的策略。这项研究纳入了 2016 年 5 月至 2021 年 5 月间同时进行 PGT 的 71 个周期的冷冻解冻和新鲜胚胎。根据来源,将来自同一患者的胚胎分为两组:解冻组和新鲜组。比较了胚胎发育、测序结果、临床和新生儿结局。结果显示,解冻组的优质胚胎率显著高于新鲜组(64.53%比 52.61%,P=0.011);然而,该组的可利用囊胚率显著低于新鲜组(47.29%比 57.83%,P=0.026)。解冻组和新鲜组分别有 96 个和 144 个囊胚进行滋养外胚层(TE)活检。解冻组的优质囊胚率显著低于新鲜组(57.29%比 70.14%,P=0.041)。两组的可遗传囊胚率无统计学差异(P=0.956)。两组的胚胎着床率、临床妊娠率、流产率和新生儿结局均无统计学差异。总之,本研究表明,卵裂期胚胎 pool 策略可能不利于维持胚胎发育潜能。如果没有必要,不建议为 PGT 进行卵裂期胚胎 pool。

相似文献

1
Accumulation of Cleavage-Stage Embryos by Vitrification may Compromise Embryonic Developmental Potential in Preimplantation Genetic Testing.玻璃化冷冻保存卵裂期胚胎可能会影响胚胎植入前遗传学检测的胚胎发育潜能。
Reprod Sci. 2022 Jun;29(6):1930-1938. doi: 10.1007/s43032-022-00880-8. Epub 2022 Feb 25.
2
Multiple vitrification-warming and biopsy procedures on human embryos: clinical outcome and neonatal follow-up of children.对人类胚胎进行多次玻璃化-复温及活检操作:儿童的临床结局及新生儿随访
Hum Reprod. 2020 Nov 1;35(11):2488-2496. doi: 10.1093/humrep/deaa236.
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The preimplantation genetic testing clinical outcomes of biopsy on vitrification-warming embryos: A retrospective study.玻璃化冷冻-复苏胚胎活检的临床结局:一项回顾性研究。
J Obstet Gynaecol Res. 2022 Jul;48(7):1621-1631. doi: 10.1111/jog.15275. Epub 2022 May 18.
4
Associations of blastocyst features, trophectoderm biopsy and other laboratory practice with post-warming behavior and implantation.囊胚特征、滋养层活检和其他实验室操作与解冻后行为和着床的关系。
Hum Reprod. 2018 Nov 1;33(11):1992-2001. doi: 10.1093/humrep/dey291.
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Live birth rate following a euploid blastocyst transfer is not affected by double vitrification and warming at cleavage or blastocyst stage.囊胚期行玻璃化冷冻与复苏不影响卵裂期或囊胚期双冻融后胚胎的活产率。
J Assist Reprod Genet. 2022 Apr;39(4):987-993. doi: 10.1007/s10815-022-02440-0. Epub 2022 Feb 26.
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Pregnancy and birth outcomes following fresh or vitrified embryo transfer according to blastocyst morphology and expansion stage, and culturing strategy for delayed development.根据囊胚形态和扩张阶段进行新鲜或玻璃化胚胎移植后的妊娠及分娩结局,以及延迟发育的培养策略。
Hum Reprod. 2016 Aug;31(8):1685-95. doi: 10.1093/humrep/dew127. Epub 2016 Jun 6.
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Double vitrification and warming of blastocysts does not affect pregnancy, miscarriage or live birth rates.玻璃化冷冻复苏的囊胚进行二次玻璃化冷冻及解冻复苏,并不影响妊娠、流产或活产率。
Reprod Biomed Online. 2024 Sep;49(3):104103. doi: 10.1016/j.rbmo.2024.104103. Epub 2024 May 6.
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A prospective randomized controlled trial investigating the effect of artificial shrinkage (collapse) on the implantation potential of vitrified blastocysts.一项前瞻性随机对照试验,研究人工皱缩(塌陷)对玻璃化囊胚着床潜能的影响。
Hum Reprod. 2015 Nov;30(11):2509-18. doi: 10.1093/humrep/dev218. Epub 2015 Sep 12.
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Effect of the Re-Vitrification of Embryos at Different Stages on Embryonic Developmental Potential.胚胎不同阶段复融对胚胎发育潜能的影响。
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Embryo pooling: a promising strategy for managing insufficient number of embryos in preimplantation genetic diagnosis.胚胎池化:一种在植入前基因诊断中应对胚胎数量不足的有前景的策略。
Gynecol Endocrinol. 2017 Nov;33(11):867-871. doi: 10.1080/09513590.2017.1347778. Epub 2017 Jul 6.

本文引用的文献

1
Fertility outcomes in women after controlled ovarian stimulation with gonadotropin releasing hormone agonist long protocol: fresh versus frozen embryo transfer.促性腺激素释放激素激动剂长方案控制性卵巢刺激后女性的生育结局:新鲜胚胎移植与冷冻胚胎移植对比
BMC Pregnancy Childbirth. 2021 Mar 12;21(1):207. doi: 10.1186/s12884-021-03698-5.
2
Repeated cryopreservation process impairs embryo implantation potential but does not affect neonatal outcomes.反复的冷冻保存过程会损害胚胎的着床潜能,但不会影响新生儿结局。
Reprod Biomed Online. 2021 Jan;42(1):75-82. doi: 10.1016/j.rbmo.2020.11.007. Epub 2020 Nov 20.
3
Thaw, biopsy and refreeze strategy for PGT-A on previously cryopreserved embryos.
针对先前冷冻保存胚胎的植入前基因检测非整倍体(PGT-A)的解冻、活检和再冷冻策略。
Facts Views Vis Obgyn. 2019 Sep;11(3):223-227.
4
Inconclusive chromosomal assessment after blastocyst biopsy: prevalence, causative factors and outcomes after re-biopsy and re-vitrification. A multicenter experience.囊胚活检后结果不确定:再次活检和重新玻璃化后发生率、原因及结局的多中心经验。
Hum Reprod. 2018 Oct 1;33(10):1839-1846. doi: 10.1093/humrep/dey282.
5
Effect of repeated cryopreservation on human embryo developmental potential.反复冻融对人类胚胎发育潜能的影响。
Reprod Biomed Online. 2017 Dec;35(6):627-632. doi: 10.1016/j.rbmo.2017.08.016. Epub 2017 Aug 24.
6
Analysis of embryo intactness and developmental potential following slow freezing and vitrification.慢速冷冻和玻璃化冷冻后胚胎完整性及发育潜能分析
Syst Biol Reprod Med. 2017 Oct;63(5):285-293. doi: 10.1080/19396368.2017.1362060. Epub 2017 Aug 10.
7
Embryo pooling: a promising strategy for managing insufficient number of embryos in preimplantation genetic diagnosis.胚胎池化:一种在植入前基因诊断中应对胚胎数量不足的有前景的策略。
Gynecol Endocrinol. 2017 Nov;33(11):867-871. doi: 10.1080/09513590.2017.1347778. Epub 2017 Jul 6.
8
The accumulation of vitrified oocytes is a strategy to increase the number of euploid available blastocysts for transfer after preimplantation genetic testing.玻璃化卵母细胞的积累是一种策略,用于在植入前基因检测后增加可用于移植的整倍体囊胚数量。
J Assist Reprod Genet. 2017 Apr;34(4):479-486. doi: 10.1007/s10815-016-0868-0. Epub 2017 Jan 9.
9
Shortened equilibration time can compromise clinical outcomes in human embryo vitrification.缩短平衡时间可能会损害人类胚胎玻璃化冷冻的临床效果。
Hum Fertil (Camb). 2016 Jun;19(2):114-9. doi: 10.1080/14647273.2016.1186848. Epub 2016 May 24.
10
Blastocysts can be rebiopsied for preimplantation genetic diagnosis and screening.囊胚可以进行再次活检以进行植入前基因诊断和筛查。
Fertil Steril. 2014 Dec;102(6):1641-5. doi: 10.1016/j.fertnstert.2014.09.018. Epub 2014 Oct 22.