Evidence map›Paper›PMID 32678284›Full record

ArticleScientific reports2020

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

Dong Wook Kwak, Shin Young Kim, Hyun Jin Kim, Ji Hyae Lim, Young-Han Kim, Hyun Mee Ryu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Expanded knowledge of cell-free DNA biology: potential to broaden the clinical utility.Extracellular vesicles and circulating nucleic acids · 2022
    Review
  10. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Dong Wook KwakDepartment of Obstetrics and Gynecology, Ajou University School of Medicine, Suwon, Korea.
Shin Young KimDepartment of Obstetrics and Gynecology, Cheil General Hospital and Women's Healthcare Center, Seoul, Korea.
Hyun Jin KimDepartment of Obstetrics and Gynecology, CHA Gangnam Medical Center, Seoul, Korea.
Ji Hyae LimCenter for Prenatal Biomarker Research, CHA Advanced Research Institute, Seongnam, Korea.
Young-Han KimDivision of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Institute of Women's Life Medical Science, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722, Korea. yhkim522@yuhs.ac.
Hyun Mee RyuCenter for Prenatal Biomarker Research, CHA Advanced Research Institute, Seongnam, Korea. hmryu2012@naver.com.
Ajou University · KRCHA University · KRCHA University Gangnam Medical Center · KRCheil General Hospital and Women's Healthcare Center · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Epigenesis, GeneticAdultBiomarkersCase-Control StudiesCell-Free Nucleic AcidsDNA MethylationEukaryotic Translation Initiation Factor 5AFemaleFetal Growth RetardationHumansInfant, NewbornInfant, Small for Gestational AgeParturitionPeptide Initiation FactorsPre-EclampsiaPregnancyBiomarkersCell-Free Nucleic AcidsEukaryotic Translation Initiation Factor 5APeptide Initiation FactorsRNA-Binding Proteins

Identifiers

PMID32678284
PMCPMC7367308
OpenAlexW3043184206

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.