Evidence map›Paper›PMID 34850562›Full record

ArticleMolecular nutrition & food research2022

Impact of In Utero Folate Exposure on DNA Methylation and Its Potential Relevance for Later-Life Health-Evidence from Mouse Models Translated to Human Cohorts.

Dieuwertje E Kok, Rebecca C Richmond, Michiel Adriaens, Chris T Evelo, Dianne Ford, John C Mathers, Natassia Robinson, Jill A McKay

Open access · hybridAbstract read
In one paragraph

Article in Molecular nutrition & food research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. 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 6 institutions in 3 countries.

Dieuwertje E KokDivision of Human Nutrition and Health, Wageningen University & Research, Wageningen, The Netherlands.
Rebecca C RichmondMRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Michiel AdriaensMaastricht Centre for Systems Biology, Maastricht University, Maastricht, The Netherlands.
Chris T EveloMaastricht Centre for Systems Biology, Maastricht University, Maastricht, The Netherlands.
Dianne FordDepartment of Applied Sciences, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.
John C MathersCentre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Human Nutrition Research Centre, Newcastle upon Tyne, UK.
Natassia RobinsonDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Jill A McKayDepartment of Applied Sciences, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.ORCID 0000-0002-2711-0301
Maastricht University Medical Centre · NLNorthumbria University · GBKarolinska Institutet · SENewcastle University · GBUniversity of Bristol · GBWageningen University & Research · NL

Funding

Biotechnology and Biological Sciences Research Council BB/G007993/1Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/5
6 · The paper itself

Abstract

scopePersistent DNA methylation changes may mediate effects of early-life exposures on later-life health. Human lifespan is challenging for prospective studies, therefore data from longitudinal studies are limited. Projecting data from mouse models of early-life exposure to human studies offers a tool to address this challenge. METHODS AND

resultsC57BL/6J mice were fed low/normal folate diets before and during pregnancy and lactation. Genome-wide promoter methylation was measured in male offspring livers at 17.5 days gestation and 28 weeks. Eight promoters were concurrently hypermethylated by folate depletion in fetuses and adults (>1.10 fold-change; p < 0.05). Processes/pathways potentially influenced by global changes, and function of these eight genes, suggest neurocognitive effects. Human observational and randomized controlled trial data were interrogated for translation. Methylation at birth was inversely associated with maternal plasma folate in six genes (-1.15% to -0.16% per nmol L

conclusionSome persistent folate-induced methylation changes in mice are mirrored in humans. This demonstrates utility of mouse data in identifying human loci for interrogation as biomarkers of later-life health.

Indexed as

DNA MethylationFolic Acid DeficiencyAdultAnimalsFemaleFolic AcidHumansMaleMiceMice, Inbred C57BLPregnancyProspective StudiesFolic Aciddevelopmental origins of health and diseaseepigeneticsfolatematernalmicetranslation

Identifiers

PMID34850562
PMCPMC7614326
OpenAlexW3215288439

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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 Socratic graph.