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miR-34a expression, epigenetic regulation, and function in human placental diseases.miR-34a 在人类胎盘疾病中的表达、表观遗传调控和功能。
Epigenetics. 2014 Jan;9(1):142-51. doi: 10.4161/epi.26196. Epub 2013 Sep 30.
2
miR-210 inhibits trophoblast invasion and is a serum biomarker for preeclampsia.微小RNA-210抑制滋养层细胞浸润,是子痫前期的一种血清生物标志物。
Am J Pathol. 2013 Nov;183(5):1437-1445. doi: 10.1016/j.ajpath.2013.07.021. Epub 2013 Sep 10.
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The promise of angiogenic markers for the early diagnosis and prediction of preeclampsia.血管生成标志物在子痫前期早期诊断和预测中的应用前景。
Clin Chem. 2012 May;58(5):837-45. doi: 10.1373/clinchem.2011.169094. Epub 2012 Mar 19.
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Gene expression in chorionic villous samples at 11 weeks of gestation in women who develop pre-eclampsia later in pregnancy: implications for screening.妊娠 11 周时绒毛样本中的基因表达与孕妇后期发生子痫前期的相关性:筛查意义。
Prenat Diagn. 2011 Feb;31(2):181-5. doi: 10.1002/pd.2675. Epub 2011 Jan 4.
5
A redox switch in angiotensinogen modulates angiotensin release.血管紧张素原中的氧化还原开关调节血管紧张素的释放。
Nature. 2010 Nov 4;468(7320):108-11. doi: 10.1038/nature09505. Epub 2010 Oct 6.
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Pre-eclampsia.子痫前期。
Lancet. 2010 Aug 21;376(9741):631-44. doi: 10.1016/S0140-6736(10)60279-6. Epub 2010 Jul 2.
7
The detrimental role of angiotensin receptor agonistic autoantibodies in intrauterine growth restriction seen in preeclampsia.血管紧张素受体激动性自身抗体在子痫前期所见的胎儿生长受限中的有害作用。
J Exp Med. 2009 Nov 23;206(12):2809-22. doi: 10.1084/jem.20090872. Epub 2009 Nov 2.
8
Overview of maternal morbidity during hospitalization for labor and delivery in the United States: 1993-1997 and 2001-2005.美国1993 - 1997年及2001 - 2005年分娩住院期间孕产妇发病情况概述
Obstet Gynecol. 2009 May;113(5):1075-1081. doi: 10.1097/AOG.0b013e3181a09fc0.
9
The two stage model of preeclampsia: variations on the theme.子痫前期的两阶段模型:主题变奏
Placenta. 2009 Mar;30 Suppl A(Suppl A):S32-7. doi: 10.1016/j.placenta.2008.11.009. Epub 2008 Dec 13.
10
Angiotensin receptor agonistic autoantibodies induce pre-eclampsia in pregnant mice.血管紧张素受体激动性自身抗体可诱发孕鼠子痫前期。
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生物标志物在子痫前期早期检测中的作用。

Role of biomarkers in early detection of preeclampsia.

作者信息

Kar Manisha

机构信息

Associate Professor, Department of Physiology, All India Institute of Medical Sciences , Bhubaneswar, Odisha, India .

出版信息

J Clin Diagn Res. 2014 Apr;8(4):BE01-4. doi: 10.7860/JCDR/2014/7969.4261. Epub 2014 Apr 15.

DOI:10.7860/JCDR/2014/7969.4261
PMID:24959436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4064886/
Abstract

Preeclampsia (PE) is a pregnancy-related, potentially life threatening condition. The incidence of PE has increased in the past decade, which has been attributed to various predisposing factors. Abnormal placentation is central to the evolution of this disease process. However, the triggering factor for this is still unknown. Interestingly, intense research done in this arena has unveiled the names of some important biomolecules which play important role in the vasculognesis of the early placenta, namely, vascular endothelial growth factor (VEGF) and placental growth factor (PlGF) and their antagonists, namely, soluble fms-like tyrosine kinase 1 (sFlt-1, also known as sVEGFR1), and soluble endoglin (sEng). Besides these, Renin Angiotensin System (RAS) was also implicated in this disease process. The roles of immune factors, genetic factors have been stressed from time to time. More novel approaches made, have shed light on the upcoming biomolecules. All these endeavours are directed to diagnose PE as early as possible, which is a real challenge. Question remains whether a single set parameters could diagnose a disease entity which is as complex as PE. Therefore, it is imperative to design feasible, predictive test-set utilizing multiple biomarkers.

摘要

子痫前期(PE)是一种与妊娠相关的、可能危及生命的疾病。在过去十年中,PE的发病率有所上升,这归因于各种诱发因素。胎盘形成异常是该疾病进程发展的核心。然而,其触发因素仍然未知。有趣的是,在这个领域进行的深入研究揭示了一些重要生物分子的名称,它们在早期胎盘的血管生成中起重要作用,即血管内皮生长因子(VEGF)和胎盘生长因子(PlGF)及其拮抗剂,即可溶性fms样酪氨酸激酶1(sFlt-1,也称为sVEGFR1)和可溶性内皮糖蛋白(sEng)。除此之外,肾素血管紧张素系统(RAS)也与该疾病进程有关。免疫因素、遗传因素的作用也时常受到强调。更多新的研究方法已经揭示了新出现的生物分子。所有这些努力都旨在尽早诊断PE,这是一项真正的挑战。问题仍然是,一组参数是否能够诊断像PE这样复杂的疾病实体。因此,利用多种生物标志物设计可行的、预测性的检测组合势在必行。