Translational Obstetrics Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, 163 Studley Rd., Heidelberg 3084, Victoria, Australia.
Expert Rev Mol Diagn. 2014 Jun;14(5):509-11. doi: 10.1586/14737159.2014.915749. Epub 2014 Apr 30.
Severe fetal hypoxia causes stillbirth and permanent childhood disability. Unfortunately, none of the current tests is precise at determining the degree of fetal hypoxia in utero. We recently showed that hypoxia-induced RNA abundance in the maternal circulation (of likely fetoplacental origin) was tightly correlated with the degree of fetal hypoxia, suggesting it may be possible to generate a maternal blood test to more precisely determine the severity of fetal hypoxia. Such a test could drastically improve outcomes and decrease stillbirth rates. We are running a large prospective study to validate this test, and will use microarrays, RNA-seq and digital PCR to identify RNA transcripts that best correlate with the severity of fetal hypoxia. Finally, we note our data hints at the possibility of measuring dynamic changes in the fetoplacental transcriptome, measured in serial maternal blood samples. This could afford exciting new insights into the pathology of major obstetric diseases.
严重的胎儿缺氧会导致死产和儿童永久性残疾。不幸的是,目前没有一种测试方法能够精确地确定胎儿在子宫内的缺氧程度。我们最近发现,母体循环中缺氧诱导的 RNA 丰度(可能来自胎-胎盘)与胎儿缺氧的程度密切相关,这表明有可能生成一种母体血液测试来更精确地确定胎儿缺氧的严重程度。这样的测试可以极大地改善结果并降低死产率。我们正在进行一项大型前瞻性研究来验证这项测试,并将使用微阵列、RNA-seq 和数字 PCR 来识别与胎儿缺氧严重程度最相关的 RNA 转录本。最后,我们注意到我们的数据提示了在连续的母体血液样本中测量胎-胎盘转录组的动态变化的可能性。这可能为主要产科疾病的病理学提供令人兴奋的新见解。