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染色体微阵列分析技术在高龄孕妇产前诊断中的应用价值
引用本文:杨舒婷,赵亚丽,汤欣欣,王志伟,刘登平,张璟璐,顾莹,王雷雷. 染色体微阵列分析技术在高龄孕妇产前诊断中的应用价值[J]. 中华医学遗传学杂志, 2021, 0(2): 101-107
作者姓名:杨舒婷  赵亚丽  汤欣欣  王志伟  刘登平  张璟璐  顾莹  王雷雷
作者单位:连云港市妇幼保健院遗传实验室
基金项目:江苏省社会发展项目(BE2018677)。
摘    要:目的:探讨染色体微阵列分析(chromosomal microarray analysis,CMA)对于高龄孕妇异常妊娠的检测价值。方法:回顾分析562例高龄孕妇的CMA检测结果、妊娠结局及新生儿的随访结果。结果:在562份羊水样本中,共检出胎儿染色体异常73例(12.99%),包括21例(3.73%)染色体非整倍体和...

关 键 词:染色体微阵列分析  高龄孕妇  产前诊断  染色体异常  拷贝数变异

Application of chromosome microarray analysis in prenatal diagnosis of pregnant women with advanced age
Yang Shuting,Zhao Yali,Tang Xinxin,Wang Zhiwei,Liu Dengping,Zhang Jinglu,Gu Ying,Wang Leilei. Application of chromosome microarray analysis in prenatal diagnosis of pregnant women with advanced age[J]. Chinese journal of medical genetics, 2021, 0(2): 101-107
Authors:Yang Shuting  Zhao Yali  Tang Xinxin  Wang Zhiwei  Liu Dengping  Zhang Jinglu  Gu Ying  Wang Leilei
Affiliation:(Laboratory of Genetics,Lianyungang Maternal and Child Health Care Hospital,Lianyangang,Jiangsu 222000,China)
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.
Keywords:Chromosomal microarray analysis  Pregnant women with advanced age  Prenatal diagnosis  Chromosomal abnormality  Copy number variation
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