Evidence map›Paper›PMID 31969597›Full record

ArticleScientific reports2020

Being Born Large for Gestational Age is Associated with Increased Global Placental DNA Methylation.

S E Dwi Putra, C Reichetzeder, A A Hasan, T Slowinski, C Chu, B K Krämer, B Kleuser, B Hocher

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
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  6. Impact of Wildland Fire Smoke PMEnvironmental science & technology · 2026
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  20. Extensive Placental Methylation Profiling in Normal Pregnancies.International journal of molecular sciences · 2021
    Article
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

8 authors at 5 institutions in 4 countries.

S E Dwi Putra *Fifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany.
C Reichetzeder *Department of Nutritional Toxicology, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany. reichetz@uni-potsdam.de.
A A HasanFifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany.
T SlowinskiDepartment of Nephrology, Campus Charité Mitte, University Hospital Charité, Berlin, Germany.
C ChuFifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany.
B K KrämerFifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany.
B KleuserDepartment of Nutritional Toxicology, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
B HocherFifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany. berthold.hocher@medma.uni-heidelberg.de.
University of Potsdam · DEUniversity Medical Centre Mannheim · DECharité - Universitätsmedizin Berlin · DEHunan Normal University · CNUniversity of Surabaya · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Being born small (SGA) or large for gestational age (LGA) is associated with adverse birth outcomes and metabolic diseases in later life of the offspring. It is known that aberrations in growth during gestation are related to altered placental function. Placental function is regulated by epigenetic mechanisms such as DNA methylation. Several studies in recent years have demonstrated associations between altered patterns of DNA methylation and adverse birth outcomes. However, larger studies that reliably investigated global DNA methylation are lacking. The aim of this study was to characterize global placental DNA methylation in relationship to size for gestational age. Global DNA methylation was assessed in 1023 placental samples by LC-MS/MS. LGA offspring displayed significantly higher global placental DNA methylation compared to appropriate for gestational age (AGA; p < 0.001). ANCOVA analyses adjusted for known factors impacting on DNA methylation demonstrated an independent association between placental global DNA methylation and LGA births (p < 0.001). Tertile stratification according to global placental DNA methylation levels revealed a significantly higher frequency of LGA births in the third tertile. Furthermore, a multiple logistic regression analysis corrected for known factors influencing birth weight highlighted an independent positive association between global placental DNA methylation and the frequency of LGA births (p = 0.001).

Indexed as

DNA MethylationGestational AgeInfant, Small for Gestational AgeAdultBirth WeightFemaleFetal MacrosomiaGenetic Association StudiesHumansPlacentaPregnancyPregnancy OutcomeYoung Adult

Identifiers

PMID31969597
PMCPMC6976643
OpenAlexW3001577803

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.