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亚甲基四氢叶酸还原酶基因多态性与胚胎染色体异常及体外受精结局无关。

Methylenetetrahydrofolate reductase gene polymorphisms are not associated with embryo chromosomal abnormalities and IVF outcomes.

机构信息

Molecular Biology, Instituto Bernabeu, Alicante, Spain.

Reproductive Embriology, Instituto Bernabeu, Alicante, Spain.

出版信息

Syst Biol Reprod Med. 2021 Aug;67(4):270-280. doi: 10.1080/19396368.2021.1923861. Epub 2021 May 30.

Abstract

The aim of our study was to investigate the effect of maternal and embryo C677T and A1298C polymorphisms on embryo aneuploidies and mosaicism and the correlation between these genetic variants in transferred euploid embryos and IVF outcomes. genotype was analyzed in 77 women who performed an IVF/ICSI cycle with PGT-A. Moreover, to evaluate the effect of embryo polymorphisms on embryo aneuploidies and mosaicism, the genotype was analyzed in 191 biopsied embryos from the PGT-A cycles of these patients. Additionally, 218 DNA samples from trophectoderm biopsies belonging to a different group of patients were also genotyped. polymorphisms were analyzed in a total amount of 409 trophectoderm samples. The main parameters analyzed were embryo aneuploidy and mosaicism rates. Finally, the IVF outcomes of 241 single euploid embryo transfers were assessed and compared between different embryo genotypes. The aneuploidy rates were similar in embryos from homozygous normal women and women with at least one mutated allele (54.7% vs. 30.2% in 677C>T and 37.8% vs. 42.7% in 1298A>C). Furthermore, no differences were observed in the mosaicism rate (24.0% vs. 13.8% in 677C>T and 17.1% vs. 17.3% in 1298A>C). A similar analysis was performed, taking into account the embryo genotype results. No differences in aneuploidy rate were observed between the study groups. The only significant difference was the mosaicism rate among 677C>T genotype (13.5% in 677CC group vs. 5.4% in 677CT/TT; p = 0.019). Implantation rate, biochemical and clinical miscarriage rates, and ongoing pregnancy rate were compared between different embryo genotypes, and no statistically significant differences were found. In conclusion, the maternal genotype did not influence embryo chromosomal abnormalities. Moreover, the embryo genotype was not associated with embryo aneuploidy or IVF outcomes such as implantation, pregnancy loss, and ongoing pregnancy when euploid embryos were transferred.: MTHFR: methylenetetrahydrofolate reductase; IVF: fertilization; PGT-A: preimplantation genetic testing for aneuploidies; SAM: S-adenosyl methionine; SNP: single nucleotide polymorphism; SPSS: Statistical Package for Social Sciences; RIF: recurrent implantation failure; RPL: recurrent pregnancy loss; hCG: human chorionic gonadotropin; PBS: phosphate buffered saline; CGH: comparative genomic hybridization; NGS: next generation sequencing.

摘要

我们的研究目的是探讨母体和胚胎 C677T 和 A1298C 多态性对胚胎非整倍体和镶嵌性的影响,以及这些遗传变异在转移的整倍体胚胎中与 IVF 结局之间的相关性。对 77 名接受 PGT-A 的 IVF/ICSI 周期的女性进行了 基因型分析。此外,为了评估胚胎 多态性对胚胎非整倍体和镶嵌性的影响,对这些患者的 PGT-A 周期中 191 个活检胚胎的 基因型进行了分析。此外,还对来自不同患者组的 218 个滋养外胚层活检 DNA 样本进行了基因分型。总共对 409 个滋养外胚层样本进行了 多态性分析。分析的主要参数是胚胎非整倍体率和镶嵌率。最后,评估了 241 例单整倍体胚胎转移的 IVF 结局,并比较了不同 胚胎基因型之间的差异。纯合正常女性和至少有一个突变等位基因的女性胚胎的非整倍体率相似(677C>T 中为 54.7% vs. 30.2%,1298A>C 中为 37.8% vs. 42.7%)。此外,镶嵌率无差异(677C>T 中为 24.0% vs. 13.8%,1298A>C 中为 17.1% vs. 17.3%)。还进行了类似的分析,考虑了胚胎基因型的结果。在研究组之间未观察到非整倍体率的差异。唯一的显著差异是 677C>T 基因型中的镶嵌率(677CC 组为 13.5%,677CT/TT 组为 5.4%;p = 0.019)。比较了不同胚胎基因型之间的着床率、生化和临床流产率以及持续妊娠率,未发现统计学差异。总之,母体 基因型并不影响胚胎染色体异常。此外,当转移整倍体胚胎时,胚胎 基因型与胚胎非整倍体或 IVF 结局(如着床、妊娠丢失和持续妊娠)无关。

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