Sahai Kavita, Saraswathy Seema, Yadav Tribhuvan Pal, Arora Devendra, Krishnan Manu
Consultant (Path & Oncopath) & Head of Department, Lab Sciences and Molecular Medicine, Army Hospital (Research & Referral), Delhi Cantt, India.
Research Scholar, Base Hospital, Delhi Cantt 110010, India.
Med J Armed Forces India. 2017 Apr;73(2):167-174. doi: 10.1016/j.mjafi.2016.09.001. Epub 2016 Nov 17.
Pre-eclampsia is a hypertensive disorder in pregnancy, which accounts for 10-15% of the maternal and perinatal mortality worldwide. Abnormal placental development and tissue hypoxia are its main etiologic factors. The present diagnostic methods of blood pressure monitoring and renal function evaluation are insufficient in the early detection of pre-eclampsia. Since molecular events portent well ahead of the disease onset, biomarker research for the early diagnosis of pre-eclampsia has recently generated ambitious clinical targets. However, no clinically validated biomarker has so far been reported for the prediction of pre-eclampsia. Therefore, this review takes stock of the current understanding of pre-eclampsia from a molecular biology perspective and critically evaluates the following diagnostic potentials claimed for the biomarkers: placental proteins, angiogenic markers, and cell-free fetal DNA (cffDNA) in maternal circulation. Though the emerging evidences in favor of the fetal-specific epigenetic marker, hypermethylated RASSF1A of cffDNA, are highlighted, it pitches for a broader strategy of 'combination biomarker approach' for the reliable forecasting and triaging of pre-eclampsia.
子痫前期是一种妊娠期高血压疾病,占全球孕产妇和围产儿死亡的10%-15%。胎盘发育异常和组织缺氧是其主要病因。目前的血压监测和肾功能评估诊断方法在子痫前期的早期检测中存在不足。由于分子事件在疾病发作前就有预兆,因此子痫前期早期诊断的生物标志物研究最近产生了雄心勃勃的临床目标。然而,迄今为止,尚未有临床验证的生物标志物可用于预测子痫前期。因此,本综述从分子生物学角度总结了目前对子痫前期的认识,并批判性地评估了以下生物标志物所宣称的诊断潜力:胎盘蛋白、血管生成标志物和母血中的游离胎儿DNA(cffDNA)。尽管强调了支持胎儿特异性表观遗传标志物——cffDNA的高甲基化RASSF1A的新证据,但它主张采用更广泛的“联合生物标志物方法”策略,以可靠地预测和分类子痫前期。