a Department of Clinical Genetics , Erasmus Medical Center , Rotterdam , the Netherlands.
Expert Rev Mol Diagn. 2016;16(5):513-20. doi: 10.1586/14737159.2016.1152890. Epub 2016 Feb 29.
It has been shown that in non-invasive prenatal testing (NIPT) there is a small chance of a false-positive or false-negative result. This is partly due to the fact that the fetal cell-free DNA present in maternal plasma is derived from the cytotrophoblast of chorionic villi (CV), which is not always representative for the fetal karyotype due to chromosomal mosaicism. Therefore, a positive NIPT result should always be confirmed with invasive testing, preferably amniocentesis, in order to investigate the fetal karyotype. However, since this invasive test can only be safely performed after 15.5 weeks of gestation while NIPT can be done from the 10(th) week of gestation, this potentially means an unacceptable long waiting time for the prospective parents to receive a definitive result. Based on our experience with cytogenetic investigations in CV and the literature, we determined whether CV sampling may be appropriate for confirmation of an abnormal NIPT result.
已经表明,在无创产前检测(NIPT)中,假阳性或假阴性结果的可能性很小。这部分是由于母体血浆中存在的胎儿游离 DNA 来源于绒毛膜绒毛的滋养层细胞(CV),由于染色体嵌合体,滋养层细胞并不总是代表胎儿核型。因此,阳性的 NIPT 结果应始终通过侵入性检测(最好是羊膜穿刺术)进行确认,以检查胎儿的核型。然而,由于这种侵入性检测只能在妊娠 15.5 周后安全进行,而 NIPT 可以从妊娠第 10 周开始进行,这可能意味着准父母需要等待很长时间才能获得明确的结果。基于我们在 CV 细胞遗传学研究方面的经验和文献资料,我们确定了 CV 取样是否可用于确认异常的 NIPT 结果。