Dar Pe'er, Shani Hagit, Evans Mark I
Department of Obstetrics & Gynecology and Women's Health, Montefiore Medical Center, Albert Einstein College of Medicine, 1695 Eastchester Road, Bronx, New York 10461, USA.
Department of Obstetrics and Gynecology, Mt. Sinai School of Medicine, New York, NY, USA; Comprehensive Genetics and Fetal Medicine Foundation of America, 131 East 65th Street, New York, NY 10065, USA.
Clin Lab Med. 2016 Jun;36(2):199-211. doi: 10.1016/j.cll.2016.01.015. Epub 2016 Mar 18.
Cell-free fetal DNA screening for Down syndrome has gained rapid acceptance over the past few years with increasing market penetration. Three main laboratory methodologies are currently used: a massive parallel shotgun sequencing (MPSS), a targeted massive parallel sequencing (t-MPS) and a single nucleotide polymorphism (SNP) based approach. Although each of these technologies has its own advantages and disadvantages, the performance of all was shown to be comparable and superior to that of traditional first-trimester screening for the detection of trisomy 21 in a routine prenatal population. Differences in performance were predominantly shown for chromosomal anomalies other than trisomy 21. Understanding the limitations and benefits of each technology is essential for proper counseling to patients. These technologies, as well as few investigational technologies described in this review, carry a great potential beyond screening for the common aneuploidies.
在过去几年中,随着市场渗透率的提高,用于唐氏综合征检测的游离胎儿DNA筛查已迅速得到认可。目前主要使用三种实验室方法:大规模平行鸟枪法测序(MPSS)、靶向大规模平行测序(t-MPS)和基于单核苷酸多态性(SNP)的方法。尽管这些技术各有优缺点,但在常规产前人群中检测21三体时,所有技术的性能都被证明具有可比性且优于传统的孕早期筛查。除21三体外,在染色体异常方面主要表现出性能差异。了解每种技术的局限性和益处对于为患者提供适当的咨询至关重要。这些技术以及本综述中描述的一些研究性技术,在筛查常见非整倍体之外具有巨大潜力。