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囊胚移植后稽留流产时残留妊娠产物的细胞遗传学分析:一项回顾性、大规模、单中心研究

Cytogenetic analysis of the retained products of conception after missed abortion following blastocyst transfer: a retrospective, large-scale, single-centre study.

作者信息

Segawa Tomoya, Kuroda Tomoko, Kato Keiichi, Kuroda Masako, Omi Kenji, Miyauchi Osamu, Watanabe Yoshiaki, Okubo Tsuyoshi, Osada Hisao, Teramoto Shokichi

机构信息

Shinbashi Yume Clinic, Excel Shinbashi, 2-5-1, Shinbashi, Minato-ku, Tokyo 105-0004, Japan.

Kato Ladies Clinic, 7-20-3, Nishi-Shinjuku, Shinjuku-ku, Tokyo 160-0023, Japan.

出版信息

Reprod Biomed Online. 2017 Feb;34(2):203-210. doi: 10.1016/j.rbmo.2016.11.005. Epub 2016 Nov 21.

Abstract

Cytogenetic analysis of the retained products of conception (POC) is the most effective test for identifying miscarriage causes. However, there has been no large-scale study limited to blastocyst transfer. This study retrospectively reports the findings of 1030 cases in which POC analysis was performed after missed abortion following single blastocyst transfer performed at the Shinbashi Yume Clinic. We identified 19.4% as normal karyotypes and 80.6% as aneuploid. These cases broke down into: 62.3% trisomy; 7.8% double trisomy; 0.5% triple or quadruple trisomy; 1.3% monosomy 21; 3.2% monosomy X; 0.1% 47,XXY; 1.0% polyploidy; 1.0% mixed; 1.1% embryonic mosaicism; and 2.4% structural anomalies. In samples with normal karyotypes, 49.5% were female while 50.5% were male. The occurrence of trisomy and double trisomy were both significantly more frequent in the ≥38 years group than in the ≤37 years group (P < 0.01). Trisomy was significantly more frequently associated with fetal heartbeat (P < 0.01); double trisomy, polyploidy and normal karyotype were significantly more frequent with no fetal heartbeat (P < 0.01). There was no significant difference in the frequency of chromosomal abnormalities between the number of miscarriages or blastocyst quality. Thus, POC cytogenetic testing is highly valuable for ascertaining the cause of miscarriage.

摘要

对稽留流产的妊娠物残留(POC)进行细胞遗传学分析是确定流产原因最有效的检测方法。然而,尚未有局限于囊胚移植的大规模研究。本研究回顾性报告了新桥梦诊所对1030例单囊胚移植后稽留流产进行POC分析的结果。我们发现19.4%为正常核型,80.6%为非整倍体。这些病例分类如下:62.3%为三体;7.8%为双三体;0.5%为三体或四体;1.3%为21号染色体单体;3.2%为X染色体单体;0.1%为47,XXY;1.0%为多倍体;1.0%为混合性;1.1%为胚胎嵌合体;2.4%为结构异常。在核型正常的样本中,49.5%为女性,50.5%为男性。≥38岁组三体和双三体的发生率均显著高于≤37岁组(P<0.01)。三体与胎儿心跳显著相关(P<0.01);双三体、多倍体和正常核型与无胎儿心跳显著相关(P<0.01)。流产次数或囊胚质量之间染色体异常的发生率无显著差异。因此,POC细胞遗传学检测对于确定流产原因具有很高的价值。

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