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Maternal total cell-free DNA in preeclampsia with and without intrauterine growth restriction
DC Field | Value | Language |
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dc.contributor.author | Kwak, DW | - |
dc.contributor.author | Kim, SY | - |
dc.contributor.author | Kim, HJ | - |
dc.contributor.author | Lim, JH | - |
dc.contributor.author | Kim, YH | - |
dc.contributor.author | Ryu, HM | - |
dc.date.accessioned | 2022-11-23T07:32:50Z | - |
dc.date.available | 2022-11-23T07:32:50Z | - |
dc.date.issued | 2020 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/22835 | - |
dc.description.abstract | 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. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Biomarkers | - |
dc.subject.MESH | Case-Control Studies | - |
dc.subject.MESH | Cell-Free Nucleic Acids | - |
dc.subject.MESH | DNA Methylation | - |
dc.subject.MESH | Epigenesis, Genetic | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fetal Growth Retardation | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Infant, Newborn | - |
dc.subject.MESH | Infant, Small for Gestational Age | - |
dc.subject.MESH | Parturition | - |
dc.subject.MESH | Peptide Initiation Factors | - |
dc.subject.MESH | Pre-Eclampsia | - |
dc.subject.MESH | Pregnancy | - |
dc.subject.MESH | Pregnancy Trimester, Second | - |
dc.subject.MESH | Pregnancy Trimester, Third | - |
dc.subject.MESH | RNA-Binding Proteins | - |
dc.title | Maternal total cell-free DNA in preeclampsia with and without intrauterine growth restriction | - |
dc.type | Article | - |
dc.identifier.pmid | 32678284 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367308 | - |
dc.subject.keyword | Predictive markers | - |
dc.subject.keyword | Biomarkers | - |
dc.subject.keyword | Genetics research | - |
dc.contributor.affiliatedAuthor | Kwak, DW | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1038/s41598-020-68842-1 | - |
dc.citation.title | Scientific reports | - |
dc.citation.volume | 10 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2020 | - |
dc.citation.startPage | 11848 | - |
dc.citation.endPage | 11848 | - |
dc.identifier.bibliographicCitation | Scientific reports, 10(1). : 11848-11848, 2020 | - |
dc.identifier.eissn | 2045-2322 | - |
dc.relation.journalid | J020452322 | - |
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