Maternal total cell-free DNA in preeclampsia with and without intrauterine growth restriction

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作者
Dong Wook Kwak
Shin Young Kim
Hyun Jin Kim
Ji Hyae Lim
Young-Han Kim
Hyun Mee Ryu
机构
[1] Ajou University School of Medicine,Department of Obstetrics and Gynecology
[2] Cheil General Hospital and Women’s Healthcare Center,Department of Obstetrics and Gynecology
[3] CHA Gangnam Medical Center,Department of Obstetrics and Gynecology
[4] CHA Advanced Research Institute,Center for Prenatal Biomarker Research
[5] Yonsei University College of Medicine,Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Institute of Women’s Life Medical Science
[6] CHA University School of Medicine,Department of Obstetrics and Gynecology, CHA Bundang Medical Center
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Elevation of total cell-free DNA (cfDNA) in patients with preeclampsia is well-known; however, whether this change precedes the onset of symptoms remains inconclusive. Here, we conducted a nested case–control study to determine the elevation of cfDNA levels in women who subsequently developed preeclampsia. Methylated HYP2 (m-HYP2) levels were determined in 68 blood samples collected from women with hypertensive disorders of pregnancy, along with 136 control samples, using real-time quantitative PCR. The measured m-HYP2 levels were converted to multiples of the median (MoM) values for correction of maternal characteristics. The m-HYP2 levels and MoM values in patients with preeclampsia were significantly higher than in controls during the third trimester (P < 0.001, both), whereas those for women who subsequently developed preeclampsia did not differ during the second trimester. However, when patients with preeclampsia were divided based on the onset-time of preeclampsia or 10th percentile birth weight, both values were significantly higher in women who subsequently developed early-onset preeclampsia (P < 0.05, both) and preeclampsia with small-for-gestational-age (SGA) neonate (P < 0.01, both) than controls. These results suggested that total cfDNA levels could be used to predict early-onset preeclampsia or preeclampsia with SGA neonate.
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