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Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia

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...

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Autores principales: Yu, Hong, Shen, Yanting, Ge, Qinyu, He, Youji, Qiao, Dongyan, Ren, Mulan, Zhang, Jianqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645703/
https://www.ncbi.nlm.nih.gov/pubmed/23567271
http://dx.doi.org/10.3390/ijms14047571
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author Yu, Hong
Shen, Yanting
Ge, Qinyu
He, Youji
Qiao, Dongyan
Ren, Mulan
Zhang, Jianqiong
author_facet Yu, Hong
Shen, Yanting
Ge, Qinyu
He, Youji
Qiao, Dongyan
Ren, Mulan
Zhang, Jianqiong
author_sort Yu, Hong
collection PubMed
description 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.
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spelling pubmed-36457032013-05-13 Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia Yu, Hong Shen, Yanting Ge, Qinyu He, Youji Qiao, Dongyan Ren, Mulan Zhang, Jianqiong Int J Mol Sci Article 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. Molecular Diversity Preservation International (MDPI) 2013-04-08 /pmc/articles/PMC3645703/ /pubmed/23567271 http://dx.doi.org/10.3390/ijms14047571 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Yu, Hong
Shen, Yanting
Ge, Qinyu
He, Youji
Qiao, Dongyan
Ren, Mulan
Zhang, Jianqiong
Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title_full Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title_fullStr Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title_full_unstemmed Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title_short Quantification of Maternal Serum Cell-Free Fetal DNA in Early-Onset Preeclampsia
title_sort quantification of maternal serum cell-free fetal dna in early-onset preeclampsia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645703/
https://www.ncbi.nlm.nih.gov/pubmed/23567271
http://dx.doi.org/10.3390/ijms14047571
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