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染色体微阵列分析在高龄孕妇产前诊断中的应用

[Application of chromosomal microarray analysis in prenatal diagnosis of pregnant women with advanced age].

作者信息

Yang Shuting, Zhao Yali, Tang Xinxin, Wang Zhiwei, Liu Dengping, Zhang Jinglu, Gu Ying, Wang Leilei

机构信息

Laboratory of Genetics, Lianyungang Maternal and Child Health Care Hospital, Lianyangang, Jiangsu 222000, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Feb 10;38(2):101-107. doi: 10.3760/cma.j.cn511374-20200323-00195.

Abstract

OBJECTIVE

To assess the value of chromosomal microarray analysis (CMA) for the detection of fetal anomalies among pregnant women with advanced age.

METHODS

CMA results of 562 cases, in addition with the outcome of pregnancy and neonatal follow-up were reviewed.

RESULTS

Among the 562 amniotic fluid samples, 73 cases (12.99%) of fetal chromosomal abnormalities were detected, which included 21 cases (3.73%) of chromosomal aneuploidies and 52 cases (9.25%) of copy number variations (CNVs). The latters included 27 cases of pathological CNVs (4.80%), 4 cases of possible pathogenic CNVs (0.71%) and 42 cases of variants with unknown clinical significance (7.47%). Compared with those under 35, the detection rate of fetal chromosomal aneuploidies for women with advanced age was higher under the indications of voluntary test, abnormal ultrasonic structures, abnormal ultrasonic soft index and risks indicated by non-invasive prenatal testing (NIPT). No significant difference was found in the detection rate of CNVs between those ≥35 and <35 and between those with age factor only and with additional indications (P> 0.05). 552 cases (98.22%) of pregnant women have completed the followed up. Among 31 women with pathological and possible pathogenic fetal CNVs detected by CMA, 25 had terminated the pregnancy, 6 (19.35%) have delivered without obvious abnormality. 41 pregnant women with fetal CNVs of unknown clinical significance have completed the follow up, among whom 3 had terminated the pregnancy, 1 newborn was found with malformation after birth, which yielded an abnormal pregnancy rate of 9.76%. 480 pregnant women with negative CMA results have completed the follow up, among whom 5 (1.04%) had abnormal pregnancy or delivered a child with birth defect.

CONCLUSION

There is a certain difference between the outcome of pregnancy predicted by CMA testing and the actual outcome. The pregnancies with fetal CNVs with unknown clinical significance detected by CMA have a high adverse rate, which should attract clinical attention. CMA testing should be recommended for pregnant women with advanced age regardless of whether they have other symptoms. CMA combined with other detection methods is the trend for prenatal diagnosis.

摘要

目的

评估染色体微阵列分析(CMA)在高龄孕妇胎儿异常检测中的价值。

方法

回顾562例病例的CMA结果以及妊娠结局和新生儿随访情况。

结果

在562份羊水样本中,检测出73例(12.99%)胎儿染色体异常,其中包括21例(3.73%)染色体非整倍体和52例(9.25%)拷贝数变异(CNV)。后者包括27例病理性CNV(4.80%)、4例可能致病性CNV(0.71%)和42例临床意义不明的变异(7.47%)。与35岁以下孕妇相比,在自愿检测、超声结构异常、超声软指标异常及无创产前检测(NIPT)提示风险等指征下,高龄孕妇胎儿染色体非整倍体的检出率更高。≥35岁与<35岁孕妇之间以及仅具有年龄因素与具有其他指征孕妇之间的CNV检出率差异无统计学意义(P>0.05)。552例(98.22%)孕妇完成了随访。在CMA检测出的31例病理性及可能致病性胎儿CNV孕妇中,25例终止妊娠,6例(19.35%)分娩时无明显异常。41例临床意义不明的胎儿CNV孕妇完成随访,其中3例终止妊娠,1例新生儿出生后发现畸形,异常妊娠率为9.76%。480例CMA结果为阴性的孕妇完成随访,其中5例(1.04%)妊娠异常或分娩出有出生缺陷的婴儿。

结论

CMA检测预测的妊娠结局与实际结局存在一定差异。CMA检测出的临床意义不明的胎儿CNV妊娠不良率较高,应引起临床重视。无论是否有其他症状,均建议高龄孕妇进行CMA检测。CMA联合其他检测方法是产前诊断的发展趋势。

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