Centre for Medical Genetics, Universitair Ziekenhuis Brussel, Laarbeeklaan 101, Brussels, Belgium.
Genome Med. 2010 Oct 6;2(10):74. doi: 10.1186/gm195.
Preimplantation genetic diagnosis (PGD) involves testing of single cells biopsied from oocytes and/or embryos generated in vitro. As only embryos unaffected for a given genetic condition are transferred to the uterus, it avoids prenatal diagnosis and termination of pregnancy. Follow-up data from PGD pregnancies, deliveries and children show an acceptable live birth rate and, so far, no detrimental effects of the procedure have been observed. Of course, the long-term health outcome is currently unknown. PGD was first performed in 1990 and remained an experimental procedure for a number of years. Now, two decades later, it is regarded as an established alternative to prenatal diagnosis: its use has expanded, the range of applications has broadened, and continuous technical progress in single-cell testing has led to high levels of efficiency and accuracy. The current gold standard methods (single-cell multiplex-PCR for monogenic diseases and interphase fluorescence in situ hybridization for chromosomal aberrations) are being replaced by single-cell whole genome amplification and array technology. These generalized methods substantially reduce the pre-PGD workload and allow more automated genome-wide analysis. The implementation of laboratory accreditation schemes brings the field at the same level of routine diagnostics. This article reviews the state of the art and considers indications, accuracy and current technical changes in the field of PGD.
胚胎植入前遗传学诊断(PGD)涉及对体外产生的卵母细胞和/或胚胎进行单细胞活检检测。由于只有未受特定遗传状况影响的胚胎被转移到子宫中,因此可以避免产前诊断和终止妊娠。PGD 妊娠、分娩和儿童的随访数据显示可接受的活产率,到目前为止,尚未观察到该程序的有害影响。当然,其长期健康结果目前尚不清楚。PGD 于 1990 年首次实施,多年来一直是一种实验性程序。现在,二十年后,它被认为是产前诊断的一种既定替代方法:其使用范围已经扩大,应用范围也已经扩大,单细胞检测的技术不断进步,效率和准确性也已经提高。目前的金标准方法(用于单基因疾病的单细胞多重 PCR 和用于染色体异常的间期荧光原位杂交)正被单细胞全基因组扩增和阵列技术所取代。这些通用方法大大减少了 PGD 的前期工作量,并允许更自动化的全基因组分析。实验室认证计划的实施使该领域达到了常规诊断的同一水平。本文综述了胚胎植入前遗传学诊断的最新技术,并考虑了该领域的适应症、准确性和当前技术变化。