Evidence map›Paper›PMID 31262346›Full record

ArticleClinical epigenetics2019

Early-life determinants of hypoxia-inducible factor 3A gene (HIF3A) methylation: a birth cohort study.

Toby Mansell, Anne-Louise Ponsonby, Vania Januar, Boris Novakovic, Fiona Collier, David Burgner, Peter Vuillermin, Joanne Ryan, Richard Saffery, Barwon Infant Study Investigator Team

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  11. Epigenetics · 2020
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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

10 authors at 2 institutions in 1 country.

Toby MansellMurdoch Children's Research Institute, Parkville, Australia.ORCID 0000-0002-1282-6331
Anne-Louise PonsonbyMurdoch Children's Research Institute, Parkville, Australia.
Vania JanuarMurdoch Children's Research Institute, Parkville, Australia.
Boris NovakovicMurdoch Children's Research Institute, Parkville, Australia.
Fiona CollierMurdoch Children's Research Institute, Parkville, Australia.
David BurgnerMurdoch Children's Research Institute, Parkville, Australia.
Peter VuillerminMurdoch Children's Research Institute, Parkville, Australia.
Joanne RyanMurdoch Children's Research Institute, Parkville, Australia.
Richard SafferyMurdoch Children's Research Institute, Parkville, Australia. richard.saffery@mcri.edu.au.
Barwon Infant Study Investigator Team
The University of Melbourne · AUBarwon Health · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethylation of the hypoxia-inducible factor 3α gene (HIF3A) has been linked to pregnancy exposures, infant adiposity and later BMI. Genetic variation influences HIF3A methylation levels and may modify these relationships. However, data in very early life are limited, particularly in association with adverse pregnancy outcomes. We investigated the relationship between maternal and gestational factors, infant anthropometry, genetic variation and HIF3A DNA methylation in the Barwon Infant Study, a population-based birth cohort. Methylation of two previously studied regions of HIF3A were tested in the cord blood mononuclear cells of 938 infants.

resultsNo compelling evidence was found of an association between birth weight, adiposity or maternal gestational diabetes with methylation at the most widely studied HIF3A region. Male sex (- 4.3%, p < 0.001) and pre-eclampsia (- 5.4%, p = 0.02) negatively associated with methylation at a second region of HIF3A; while positive associations were identified for gestational diabetes (4.8%, p = 0.01) and gestational age (1.2% increase per week, p < 0.001). HIF3A genetic variation also associated strongly with methylation at this region (p < 0.001).

conclusionsPre- and perinatal factors impact HIF3A methylation, including pre-eclampsia. This provides evidence that specific pregnancy complications, previously linked to adverse outcomes for both mother and child, impact the infant epigenome in a molecular pathway critical to several vascular and metabolic conditions. Further work is required to understand the mechanisms and clinical relevance, particularly the differing effects of in utero exposure to gestational diabetes or pre-eclampsia.

Indexed as

DNA MethylationAdultApoptosis Regulatory ProteinsBirth WeightCohort StudiesCpG IslandsDiabetes, GestationalEpigenesis, GeneticFemaleGenetic Association StudiesGestational AgeHumansIncidenceInfant, NewbornMalePre-EclampsiaApoptosis Regulatory ProteinsHIF3A protein, humanRepressor ProteinsDNA methylationGestational diabetesHIF3AInfantPre-eclampsiaPregnancySNPs

Identifiers

PMID31262346
PMCPMC6604333
OpenAlexW2954677902

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Registered trials

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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.