Lo Y M Dennis
Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong Special Administrative Region, China.
J Histochem Cytochem. 2005 Mar;53(3):293-6. doi: 10.1369/jhc.4R6362.2005.
The discovery of cell-free fetal DNA in maternal plasma in 1997 has opened up new possibilities for noninvasive prenatal diagnosis. Circulating fetal DNA molecules have been detected in maternal plasma from the first trimester onwards and can be robustly detected using a variety of molecular methods. This approach has been used for the prenatal investigation of sex-linked diseases, fetal RhD status, and prenatal exclusion of beta-thalassemia major. Recently, fetal RNA has also been found in maternal plasma. Such fetal RNA has been shown to originate from the placenta and to be remarkably stable. The use of microarray-based approaches has made it feasible to rapidly generate new circulating RNA markers. It is hoped that further developments in this field will make the routine and widespread practice of noninvasive nucleic acid-based prenatal diagnosis for common pregnancy-associated disorders feasible in the near future.
1997年在母体血浆中发现游离胎儿DNA,为无创产前诊断开辟了新的可能性。从妊娠早期开始,就已在母体血浆中检测到循环胎儿DNA分子,并且可以使用多种分子方法进行可靠检测。这种方法已用于性连锁疾病的产前调查、胎儿RhD状态以及重型β地中海贫血的产前排除。最近,在母体血浆中也发现了胎儿RNA。已证明这种胎儿RNA起源于胎盘且非常稳定。基于微阵列的方法使快速生成新的循环RNA标志物成为可能。希望该领域的进一步发展将使基于核酸的无创产前诊断在不久的将来用于常见妊娠相关疾病的常规和广泛应用成为可行。