First-trimester chorionic villus sampling: genetic analysis of 985 cases

Yu-long Tong, H. Pan, Kaiping Wei, Jie Fu, Li Yu, Huixia Yang
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Abstract

Objective To investigate the value and safety of first-trimester chorionic villus sampling (CVS) in prenatal diagnosis. Methods This study retrospectively analyzed the clinical data of 985 cases undergoing CVS and prenatal diagnosis with karyotyping and fluorescence in situ hybridization (FISH) in the Department of Obstetrics and Gynecology of Peking University First Hospital from January 2012 to December 2017. The success rate of cell culture, indications for prenatal diagnosis, karyotyping results, and complications of CVS were described. Results Among the 985 cases, 970 (98.48%) underwent FISH and 893 (90.66%) received karyotyping, and 878 (89.14%) accepted both. After CVS, the success rate of cell culture was 96.64% (863/893). Abnormal ultrasonographic findings (42.64%, 420/985) were the most common indications for prenatal diagnosis. In this study, 181 cases of chromosomal abnormalities were detected, including numerical and structural abnormalities, accounting for 18.38% of all 985 cases. Those cases with abnormal ultrasonographic images had the highest detection rate of chromosomal abnormalities (31.90%, 134/420), followed by those with adverse pregnant history (11.83%, 20/169) and advanced maternal age (8.21%, 11/134). In addition, there was a discrepancy between karyotyping and FISH results, which might due to 16 cases of placental mosaicism and 13 cases of maternal cell contamination (MCC). Embryonic demises were reported in six cases (0.61%, 6/985), including four with chromosomal numerical abnormalities within four weeks after CVS. No other short- or long-term postoperative complications were found in the rest 979 cases (99.39%). Conclusions CVS in the first trimester is a safe and reliable invasive method for prenatal diagnosis, which can help to obtain an earlier diagnosis in a certain population such as those with abnormal ultrasonographic findings, thus improve the pertinence and efficiency of prenatal diagnosis. However, the potential influences of placental mosaicism and MCC on the diagnostic results should not be ignored. Key words: Chorionic villi sampling; Prenatal diagnosis; Chromosome aberrations; Pregnancy trimester, first
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妊娠早期绒毛膜绒毛取样:985例遗传分析
目的探讨孕早期绒毛取样(CVS)在产前诊断中的价值和安全性。方法回顾性分析2012年1月至2017年12月北京大学第一医院妇产科985例经CVS及核型分析和荧光原位杂交(FISH)产前诊断的临床资料。介绍了细胞培养的成功率、产前诊断的指征、核型分析结果和CVS的并发症。结果985例中,970例(98.48%)接受了FISH,893例(90.66%)接受了核型分析,878例(89.14%)接受了两者。CVS后,细胞培养成功率为96.64%(863/893)。超声检查异常(42.64%,420/985)是最常见的产前诊断指征。在这项研究中,共检测到181例染色体异常,包括数量和结构异常,占全部985例的18.38%。超声图像异常的患者染色体异常检出率最高(31.90%,134/420),其次是有不良妊娠史的患者(11.83%,20/169)和高龄产妇(8.21%,11/134)。此外,核型分析和FISH结果之间存在差异,这可能是由于16例胎盘嵌合体和13例母体细胞污染(MCC)。据报道,有6例(0.61%,6/985)发生胚胎性白血病,其中4例在CVS后四周内出现染色体数量异常。其余979例(99.39%)未发现其他短期或长期的术后并发症。结论孕早期CVS是一种安全可靠的有创产前诊断方法,有助于在超声检查异常等人群中获得早期诊断,从而提高产前诊断的针对性和效率。然而,不应忽视胎盘嵌合体和MCC对诊断结果的潜在影响。关键词:绒毛取样;产前诊断;染色体畸变;妊娠三个月,第一次
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中华围产医学杂志
中华围产医学杂志 Medicine-Obstetrics and Gynecology
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