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使用PGTseq(一种用于植入前基因检测-非整倍体的靶向新一代测序平台)对初始滋养外胚层活检结果与胚胎其他部分进行的一致性率。

The concordance rates of an initial trophectoderm biopsy with the rest of the embryo using PGTseq, a targeted next-generation sequencing platform for preimplantation genetic testing-aneuploidy.

作者信息

Kim Julia, Tao Xin, Cheng Michael, Steward Ayesha, Guo Vanessa, Zhan Yiping, Scott Richard T, Jalas Chaim

机构信息

IVIRMA Basking Ridge, New Jersey; Sidney Kimmel Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania.

Foundation for Embryonic Competence, Basking Ridge, New Jersey.

出版信息

Fertil Steril. 2022 Feb;117(2):315-323. doi: 10.1016/j.fertnstert.2021.10.011. Epub 2021 Dec 31.

Abstract

OBJECTIVE

To determine how often the results of a single trophectoderm (TE) biopsy tested by PGTseq, a targeted next-generation sequencing preimplantation genetic testing for aneuploidy technology, reflect the biology of the rest of the embryo.

DESIGN

Blinded prospective cohort study.

SETTING

University-affiliated private practice.

PATIENT(S): A total of 300 blastocysts were donated; 113 of these embryos were euploid; 163 embryos possessed at least one whole chromosome aneuploidy; and 24 embryos were negative for whole chromosome aneuploidy but possessed at least one secondary finding on initial TE biopsy.

INTERVENTION(S): All blastocysts underwent rebiopsy and preimplantation genetic testing for aneuploidy on the PGTseq platform.

MAIN OUTCOME MEASURE(S): Partial concordance rate per embryo, total concordance rate per embryo, and total concordance rate per chromosomal event.

RESULT(S): An initial TE biopsy result of euploidy or whole chromosome aneuploidy was reconfirmed in >99% of rebiopsied samples, affirming that meiotic errors are manifested in almost the entire embryo. In contrast, results of whole chromosome or segmental mosaicism were confirmed in 15%-18% of subsequent rebiopsies, suggesting that mitotic events are only sporadically seen throughout the embryo. Segmental aneuploidy was confirmed in 56.6% of rebiopsied samples, identifying a mixed meiotic and mitotic etiology for such abnormalities.

CONCLUSION(S): A euploid or aneuploid result on the PGTseq platform is highly concordant with the rest of the embryo's ploidy status. The rarer confirmation of whole chromosome mosaic and segmental mosaic results suggest that these mosaics are suitable for embryo transfer. Segmental aneuploidy, with higher concordance rates throughout the embryo, may represent a different biologic etiology compared to mosaic embryos.

摘要

目的

确定通过对单卵裂球(TE)活检进行PGTseq检测(一种针对非整倍体技术的靶向新一代测序植入前基因检测)的结果反映胚胎其余部分生物学特性的频率。

设计

盲法前瞻性队列研究。

地点

大学附属私人诊所。

患者

总共捐赠了300个囊胚;其中113个胚胎为整倍体;163个胚胎至少有一条全染色体非整倍体;24个胚胎全染色体非整倍体检测为阴性,但在初次TE活检时有至少一项次要发现。

干预措施

所有囊胚均接受再次活检,并在PGTseq平台上进行非整倍体植入前基因检测。

主要观察指标

每个胚胎的部分一致性率、每个胚胎的总一致性率以及每个染色体事件的总一致性率。

结果

在>99%的再次活检样本中,初次TE活检的整倍体或全染色体非整倍体结果得到再次确认,证实减数分裂错误几乎在整个胚胎中表现出来。相比之下,在随后15%-18%的再次活检中确认了全染色体或节段性嵌合的结果,表明有丝分裂事件仅偶尔在整个胚胎中出现。在56.6%的再次活检样本中确认了节段性非整倍体,确定了此类异常的减数分裂和有丝分裂混合病因。

结论

PGTseq平台上的整倍体或非整倍体结果与胚胎其余部分的倍性状态高度一致。全染色体嵌合和节段性嵌合结果的较少确认表明这些嵌合体适合胚胎移植。节段性非整倍体在整个胚胎中的一致性率较高,与嵌合胚胎相比可能代表不同的生物学病因。

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