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在高危妊娠中使用染色体微阵列分析进行产前诊断。

Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk Pregnancies.

作者信息

Hsiao Ching-Hua, Chen Jia-Shing, Shiao Yu-Ming, Chen Yann-Jang, Chen Ching-Hsuan, Chu Woei-Chyn, Wu Yi-Cheng

机构信息

Department of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.

Department of Obstetrics and Gynecology, Taipei City Hospital, Women and Children Campus, Taipei 100, Taiwan.

出版信息

J Clin Med. 2022 Jun 23;11(13):3624. doi: 10.3390/jcm11133624.

Abstract

Background: To assess the value of chromosomal microarray analysis (CMA) during the prenatal diagnosis of high-risk pregnancies. Methods: Between January 2016 and November 2021, we included 178 chorionic villi and 859 amniocentesis samples from consecutive cases at a multiple tertiary hospital. Each of these high-risk singleton pregnancies had at least one of the following indications: (1) advanced maternal age (AMA; ≥35 years; 546, 52.7%); (2) fetal structural abnormality on ultrasound (197, 19.0%); (3) high-risk first- or second-trimester Down syndrome screen (189, 18.2%), including increased nuchal translucency (≥3.5 mm; 90, 8.7%); or (4) previous pregnancy, child, or family history (105, 10.1%) affected by chromosomal abnormality or genetic disorder. Both G-banding karyotype analysis and CMA were performed. DNA was extracted directly and examined with oligonucleotide array-based comparative genomic hybridization. Results: Aneuploidies were detected by both G-banding karyotyping and CMA in 42/1037 (4.05%) cases. Among the 979 cases with normal karyotypes, 110 (10.6%) cases had copy number variants (CNVs) in CMA, including 30 (2.9%) cases with reported pathogenic and likely pathogenic CNVs ≥ 400 kb, 37 (3.6%) with nonreported VOUS, benign, or likely benign CNVs ≥ 400 kb, and 43 (4.1%) with nonreported CNVs < 400 kb. Of the 58 (5.6%) cases with aneuploidy rearrangements, 42 (4.1%) were diagnosed by both G-banding karyotyping and CMA; four inversions, six balanced translocations, and six low mosaic rates were not detected with CMA. Conclusions: CMA is an effective first step for the prenatal diagnosis of high-risk pregnancies with fetal structural anomalies found in ultrasonography or upon positive findings.

摘要

背景

评估染色体微阵列分析(CMA)在高危妊娠产前诊断中的价值。方法:2016年1月至2021年11月期间,我们纳入了一家三级综合医院连续病例中的178例绒毛膜绒毛样本和859例羊水样本。这些高危单胎妊娠中的每一例至少有以下指征之一:(1)高龄产妇(AMA;≥35岁;546例,52.7%);(2)超声检查发现胎儿结构异常(197例,19.0%);(3)孕早期或孕中期唐氏综合征筛查高危(189例,18.2%),包括颈项透明层增厚(≥3.5mm;90例,8.7%);或(4)既往妊娠、子女或家族史(105例,10.1%)受染色体异常或遗传疾病影响。同时进行了G显带核型分析和CMA。直接提取DNA并采用基于寡核苷酸阵列的比较基因组杂交技术进行检测。结果:在1037例样本中,42例(4.05%)通过G显带核型分析和CMA均检测到非整倍体。在979例核型正常的病例中,110例(10.6%)在CMA中检测到拷贝数变异(CNV),其中30例(2.9%)为已报道的致病性和可能致病性CNV≥400kb,37例(3.6%)为未报道的意义不明的变异(VOUS)、良性或可能良性的CNV≥400kb,43例(4.1%)为未报道的CNV<400kb。在58例(5.6%)非整倍体重排病例中,42例(4.1%)通过G显带核型分析和CMA均被诊断出来;4例倒位、6例平衡易位和6例低嵌合率病例未被CMA检测到。结论:对于超声检查发现胎儿结构异常或检查结果呈阳性的高危妊娠,CMA是产前诊断的有效第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53e1/9267905/771576a42a0b/jcm-11-03624-g001.jpg

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