, London, UK.
J Assist Reprod Genet. 2020 Mar;37(3):673-676. doi: 10.1007/s10815-020-01712-x. Epub 2020 Feb 5.
Preimplantation genetic testing for aneuploidy (PGT-A) does not create normal embryos, but selecting a viable embryo for a fresh transfer has the potential to deliver an extra effect for live birth from a stimulated cycle by evading the attrition associated with embryo cryopreservation. Improved genetic tests are now available for selecting viable embryos; however, current embryo cryopreservation techniques also have a superior survival rate, which means it is now possible to transfer most morphologically suitable embryos from a stimulated cycle one at a time. The cumulative live birth rate from a stimulated cycle is now unlikely to be superior compared with morphological assessment alone, with any benefit likely to be associated with a reduction in the risk of miscarriage and the time to pregnancy. This communication offers a perspective on the likely benefit and disbenefit of PGT-A based on the outcome of modern-day clinical studies. Caution should be advised regarding offering PGT-A to every woman. Quantifying the likely miscarriage benefit and live birth disbenefit for an appropriate patient group may help to better inform couples who might be considering adding aneuploidy screening to their treatment cycle.
胚胎植入前遗传学检测(PGT-A)并不能创造正常胚胎,但选择一个可行的胚胎进行新鲜移植,通过避免与胚胎冷冻相关的损耗,有可能为刺激周期的活产带来额外的效果。现在有更好的基因检测技术可用于选择可行的胚胎;然而,目前的胚胎冷冻技术也具有更高的存活率,这意味着现在可以一次从刺激周期中转移大多数形态学上合适的胚胎。与单纯的形态评估相比,刺激周期的累积活产率不太可能更高,其益处可能与降低流产风险和妊娠时间相关。本通讯基于现代临床研究的结果,对 PGT-A 的可能获益和风险进行了评估。对于每位女性提供 PGT-A 都应谨慎。对于合适的患者群体,量化可能的流产获益和活产风险,可能有助于更好地为那些可能考虑将非整倍体筛查添加到其治疗周期的夫妇提供信息。