Kane Stefan C, Reidy Karen L, Norris Fiona, Nisbet Deborah L, Kornman Louise H, Palma-Dias Ricardo
Pregnancy Research Centre, Department of Maternal Fetal Medicine, The Royal Women's Hospital, Parkville, VIC, Australia.
The University of Melbourne, Department of Obstetrics and Gynaecology, The Royal Women's Hospital, Parkville, VIC, Australia.
Prenat Diagn. 2017 Apr;37(4):399-408. doi: 10.1002/pd.5026. Epub 2017 Mar 12.
To quantify the impact of cell-free DNA (cfDNA) screening on chorionic villus sampling (CVS) test indications and outcomes in a tertiary maternity service.
Retrospective cohort study of all CVS procedures performed for any indication on singleton pregnancies at The Royal Women's Hospital, Melbourne, and at Women's Ultrasound Melbourne, Australia, between August 2008 and February 2015. Karyotypes were classified according to pathogenicity and detectability by standard cfDNA screening panels.
A total of 2051 CVS procedures, 25 373 twelve-week scans and 2394 cfDNA tests were performed. The CVS rate per 12-week scan fell from 9.8 to 3.9% following introduction of cfDNA screening. The yield of pathogenic chromosomal anomalies per CVS increased from 12.9 to 25.2%, with 70% of pathogenic results now comprising T21, up from 52%. Sixteen (5.3%) of the pathogenic chromosomal abnormalities identified on CVS would not have been predicted by current cfDNA tests.
There is an evolving tension between improved screening performance for common aneuploidies offered by cfDNA testing, and the increasing diagnostic utility of molecular karyotyping. However, the risk of not identifying pathogenic chromosomal abnormalities is low if cfDNA screening is offered in the absence of a structural fetal anomaly, increased nuchal translucency or relevant family history. © 2017 John Wiley & Sons, Ltd.
量化游离DNA(cfDNA)筛查对三级产科服务中绒毛取样(CVS)检测指征和结果的影响。
对2008年8月至2015年2月期间在澳大利亚墨尔本皇家妇女医院和墨尔本妇女超声中心因任何指征对单胎妊娠进行的所有CVS手术进行回顾性队列研究。根据标准cfDNA筛查面板的致病性和可检测性对核型进行分类。
共进行了2051例CVS手术、25373次孕12周扫描和2394次cfDNA检测。引入cfDNA筛查后,每12周扫描的CVS率从9.8%降至3.9%。每次CVS中致病性染色体异常的检出率从12.9%提高到25.2%,现在70%的致病性结果为T21,高于之前的52%。CVS中鉴定出的16例(5.3%)致病性染色体异常无法通过当前的cfDNA检测预测。
cfDNA检测对常见非整倍体筛查性能的改善与分子核型分析诊断效用的增加之间的矛盾日益凸显。然而,如果在没有结构性胎儿异常、颈项透明层增厚增加或相关家族史的情况下进行cfDNA筛查,未识别致病性染色体异常的风险较低。©2017约翰威立父子有限公司。