β-globin DNA in maternal plasma as a molecular marker of pre-eclampsia

β-globin DNA in maternal plasma as a molecular marker of pre-eclampsia
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DOI:
10.1002/pd.965
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发表时间:
2004-09-01
期刊:
影响因子:
3
通讯作者:
Okai, T
Okai, T
中科院分区:
医学2区
文献类型:
--
作者:
Sekizawa, A;Farina, A;Okai, T

文献摘要

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目的在先兆子痫(PE)的临床特征存在下,母体血浆中无细胞胎儿DNA的水平较高。然而,目前,该方法仅在携带男性胎儿的女性中通过扩增Y特异性序列提供信息。在本研究中,我们克服了这一限制,通过检查β-珠蛋白,胎儿性别无关的DNA marker.Methods的定量分布,我们定量β-珠蛋白浓度在血浆中的207名孕妇:对照组,164名受试者,受影响的组,43名妇女受PE(n = 43)。β-珠蛋白浓度被转换成对照组中位数(MoM)的倍数,以评估β-珠蛋白MoM在病例组和对照组中可能的不同分布。结果调整后的MoM值如下:对照组,1.00 +/- 0.71;患病组4.03 +/- 3.77(P值< 0.001)。在PE患者中,胎儿生长受限(FGR)患者的MoM β-珠蛋白值几乎是无FGR患者的2倍(p值= 0.003)。结论PE患者血浆β-珠蛋白水平较高,尤其是合并FGR的患者,且与胎儿性别无关。这样的分子标记物可以潜在地用于评估PE的病理生理严重性。版权所有(C)2004约翰威利父子有限公司。
Objectives Levels of cell-free foetal DNA in maternal plasma are higher in the presence of clinical features of pre-eclampsia (PE). However, currently, this method is informative only in women bearing a male foetus, by amplification of Y-specific sequences. In the present study, we overcame this limitation by examining quantitative distribution of beta-globin, a foetal gender- independent DNA marker.Methods We quantified beta-globin concentrations in the plasma of 207 pregnant women: control group, 164 subjects; affected group, 43 women affected by PE (n = 43). beta-globin concentrations were converted into multiples of the median of the controls (MoM), in order to assess the possible different distribution of beta-globin MoM in cases and controls.Results Adjusted MoM values were as follows: controls, 1.00 +/- 0.71; affected group 4.03 +/- 3.77 (P-value < 0.001). Among the PE affected cases, MoM beta-globin values of cases with foetal growth restriction (FGR) were almost twice as great as those cases without FGR (p-value = 0.003).Conclusion beta-globin levels are higher in the plasma of pregnant women with PE, especially in those cases complicated with FGR, and do not depend on foetal gender. Such a molecular marker can potentially be used in evaluating the pathophysiological severity of PE. Copyright (C) 2004 John Wiley Sons, Ltd.