Saraswathy Seema, Sahai Kavita, Arora Devendra, Krishnan Manu, Mendiratta Suman Lata, Biswas Shilpie, Abraham Kurian Mathew
a Base Hospital, Delhi Cantt, School of Medicine & Paramedical Health Sciences, Guru Gobind Singh Indraprastha University , Delhi , India.
b Department of Pathology , Armed Forces Medical College (AFMC) , Pune , India.
J Matern Fetal Neonatal Med. 2017 Apr;30(7):849-853. doi: 10.1080/14767058.2016.1188917. Epub 2016 Jun 13.
To quantify cell free fetal DNA (cffDNA) with fetal specific epigenetic marker, hypermethylated RASSF1A, in maternal plasma of normal pregnant women from 20 weeks of gestation and to assess its relationship with maternal age, height, pre-pregnancy weight and body mass index (BMI).
Hundred normal pregnant women within the gestational age of 21-40 weeks were randomly selected and grouped into five (n = 20). Group 1: 21-24, Group 2: 25-28, Group 3: 29-32, Group 4: 33-36 and Group 5: 37-40 weeks. Maternal plasma DNA was extracted, digested with methylation-sensitive restriction enzyme, BstUI and the fetal specific DNA (cffDNA) was quantified by Real-time polymerase chain reaction (qRT-PCR).
The mean hypermethylated RASSF1A concentrations in different gestational groups were Group 1: 30.1 ± 14.9, Group 2: 52.6 ± 22.18, Group 3: 93.2 ± 19.08, Group 4: 172.8 ± 26.81 and Group 5: 337.8 ± 52.9 copies/ml. Pearson's correlation analysis showed highly significant positive correlation between cffDNA and gestational age (r = 0.899, p < 0.001). BMI was also found to be positively related to cffDNA (r = 0.217, p < 0.05). However, it did not show any correlation with maternal age, height and pre-pregnancy weight.
The gestational age-dependent increase of hypermethylated RASSF1A; the fetal specific epigenetic marker in maternal plasma was demonstrated, in an Indian study group of normal pregnant women. Findings would form the basis of future studies involving pregnancy complications that would aid in the early diagnosis of placental pathologies with hypermethylated RASSF1A.
对妊娠20周起正常孕妇母血中携带胎儿特异性表观遗传标记——高甲基化RASSF1A的游离胎儿DNA(cffDNA)进行定量,并评估其与孕妇年龄、身高、孕前体重及体重指数(BMI)的关系。
随机选取100名孕龄在21 - 40周的正常孕妇,分为五组(每组n = 20)。第1组:21 - 24周,第2组:25 - 28周,第3组:29 - 32周,第4组:33 - 36周,第5组:37 - 40周。提取母血DNA,用甲基化敏感限制性内切酶BstUI消化,通过实时聚合酶链反应(qRT-PCR)对胎儿特异性DNA(cffDNA)进行定量。
不同孕周组高甲基化RASSF1A的平均浓度分别为:第1组:30.1±14.9,第2组:52.6±22.18,第3组:93.2±19.08,第4组:172.8±26.81,第5组:337.8±52.9拷贝/毫升。Pearson相关性分析显示,cffDNA与孕周呈高度显著正相关(r = 0.899,p < 0.001)。还发现BMI与cffDNA呈正相关(r = 0.217,p < 0.05)。然而,其与孕妇年龄、身高及孕前体重无相关性。
在一组印度正常孕妇研究中证实,母血中胎儿特异性表观遗传标记高甲基化RASSF1A的浓度随孕周增加而升高。这些发现将为未来涉及妊娠并发症的研究奠定基础,有助于利用高甲基化RASSF1A早期诊断胎盘病变。