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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.

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。

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