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早发型子痫前期孕妇血清游离胎儿DNA的定量分析

Quantification of maternal serum cell-free fetal DNA in early-onset preeclampsia.

作者信息

Yu Hong, Shen Yanting, Ge Qinyu, He Youji, Qiao Dongyan, Ren Mulan, Zhang Jianqiong

机构信息

Department of Obstetrics and Gynecology, Zhongda Hospital, Medical School, Southeast University, Nanjing 210009, China.

出版信息

Int J Mol Sci. 2013 Apr 8;14(4):7571-82. doi: 10.3390/ijms14047571.

Abstract

The aim of this study was to determine whether the increased serum cell-free fetal DNA (cffDNA) level of gravidas developed into early-onset preeclampsia (EOPE) subsequently in the early second trimesters is related to prenatal screening markers. Serum was collected from 1011 gravidas. The level of cffDNA and prenatal screening markers were analyzed in 20 cases with EOPE and 20 controls. All fetuses were male. The maternal serum cffDNA level was assessed by amplification of the Y chromosome specific gene. Correlations between the variables were examined. (Logged) cffDNA in EOPE (median, 3.08; interquartile range, 2.93-3.68) was higher than controls (median, 1.79; interquartile range, 1.46-2.53). The increased level of (logged) cffDNA was correlated significantly with the increased human chorionic gonadotropin (HCG) level (r = 0.628, p < 0.001). Significant reciprocal correlations between cffDNA and babies' birth weight as well as gestation weeks at delivery were noted (r = -0.516, p = 0.001; r = -0.623, p < 0.001, respectively). The sensitivity and specificity of cffDNA to discriminate between the EOPE cases and the controls were 90% and 85%, respectively. CffDNA is a potential marker for EOPE, which had a significant reciprocal correlation with babies' birth weight and gestation weeks at delivery. Moreover, it may help in indicating the underlying hypoxic condition in the placenta.

摘要

本研究的目的是确定孕中期早期血清中游离胎儿DNA(cffDNA)水平升高随后发展为早发型子痫前期(EOPE)的孕妇是否与产前筛查标志物有关。收集了1011名孕妇的血清。对20例早发型子痫前期患者和20例对照者的cffDNA水平和产前筛查标志物进行了分析。所有胎儿均为男性。通过扩增Y染色体特异性基因评估孕妇血清cffDNA水平。检查了变量之间的相关性。早发型子痫前期患者的(对数)cffDNA(中位数为3.08;四分位数间距为2.93 - 3.68)高于对照组(中位数为1.79;四分位数间距为1.46 - 2.53)。(对数)cffDNA水平升高与人类绒毛膜促性腺激素(HCG)水平升高显著相关(r = 0.628,p < 0.001)。cffDNA与婴儿出生体重以及分娩时孕周之间存在显著的负相关(分别为r = -0.516,p = 0.001;r = -0.623,p < 0.001)。cffDNA区分早发型子痫前期病例和对照组的敏感性和特异性分别为90%和85%。CffDNA是早发型子痫前期的一个潜在标志物,它与婴儿出生体重和分娩时孕周存在显著的负相关。此外,它可能有助于提示胎盘潜在的缺氧状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1983/3645703/efec55abe037/ijms-14-07571f1.jpg

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