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胚胎产物的遗传学分析及 PGT 在早期妊娠丢失管理中的作用。

Role of genetic analysis of products of conception and PGT in managing early pregnancy loss.

机构信息

Natera, Inc., San Carlos, CA, USA.; Department of Obstetrics and Gynecology, University of Tennessee Health Sciences Center, Memphis, TN, USA..

Department of Obstetrics and Gynecology, University of Balamand, Beirut, Lebanon.

出版信息

Reprod Biomed Online. 2024 Jul;49(1):103738. doi: 10.1016/j.rbmo.2023.103738. Epub 2023 Nov 26.

Abstract

This article considers the addition of comprehensive 24-chromosomal microarray (CMA) analysis of products of conception (POC) to a standard evaluation for recurrent pregnancy loss (RPL) to help direct treatment towards expectant management versus IVF with preimplantation genetic testing for aneuploidies (PGT-A). The review included retrospective data from 65,333 miscarriages, a prospective evaluation of 378 couples with RPL who had CMA testing of POC and the standard workup, and data from an additional 1020 couples who were evaluated for RPL but did not undergo CMA testing of POC. Aneuploidy in POC explained the pregnancy loss in 57.7% (218/378) of cases. In contrast, the full RPL evaluation recommended by the American Society for Reproductive Medicine identified a potential cause in only 42.9% (600/1398). Combining the data from the RPL evaluation and the results of genetic testing of POC provides a probable explanation for the loss in over 90% (347/378) of women. Couples with an unexplained loss after the standard evaluation with POC aneuploidy accounted for 41% of cases; PGT-A may be considered after expectant management. Conversely, PGT-A would have a limited role in those with a euploid loss and a possible explanation after the standard workup. Categorizing a pregnancy loss as an explained versus unexplained loss after the standard evaluation combined with the results of CMA testing of POC may help identify patients who would benefit from expectant management versus PGT-A.

摘要

本文考虑在常规复发性妊娠丢失(RPL)评估中增加全面的 24 条染色体微阵列(CMA)分析产物(POC),以帮助将治疗方向转向期待管理而非体外受精(IVF)联合胚胎植入前遗传学检测非整倍体(PGT-A)。该综述纳入了 65333 例流产的回顾性数据、378 对 RPL 夫妇的前瞻性评估,他们进行了 CMA 检测 POC 和标准检查,以及另外 1020 对评估 RPL 但未进行 POC CMA 检测的夫妇的数据。POC 的非整倍体解释了 57.7%(218/378)病例的妊娠丢失。相比之下,美国生殖医学协会推荐的完整 RPL 评估仅能确定 42.9%(600/1398)的潜在原因。将 RPL 评估数据和 POC 遗传检测结果相结合,为超过 90%(347/378)的女性提供了可能的丢失原因解释。在 POC 非整倍体标准评估后不明原因丢失的夫妇占 41%;可以考虑在期待管理后进行 PGT-A。相反,对于整倍体丢失和标准检查后可能有解释的夫妇,PGT-A 的作用有限。在标准评估结合 POC CMA 检测后将妊娠丢失分类为有解释或无解释丢失,可能有助于确定需要期待管理还是 PGT-A 的患者。

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