Evidence map›Paper›PMID 23917818›Full record

ArticleEpigenetics2013

Association of maternal and nutrient supply line factors with DNA methylation at the imprinted IGF2/H19 locus in multiple tissues of newborn twins.

Yuk Jing Loke, John C Galati, Ruth Morley, Eric Ji-Hoon Joo, Boris Novakovic, Xin Li, Blaise Weinrich, Nicole Carson, Miina Ollikainen, Hong-Kiat Ng and 4 more

Open access · bronzeAbstract readTwin Study
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. DNA methylation differences at birth after conception through ART.Human reproduction (Oxford, England) · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Alcohol-Induced Developmental Origins of Adult-Onset Diseases.Alcoholism, clinical and experimental research · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Silver nanoparticles cause complications in pregnant mice.International journal of nanomedicine · 2015
    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

14 authors at 2 institutions in 4 countries.

Yuk Jing LokeDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Early Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
John C GalatiClinical Epidemiology and Biostatistics Unit; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia; Department of Mathematics and Statistics; La Trobe University; Melbourne, VIC Australia.
Ruth MorleyEarly Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Eric Ji-Hoon JooDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Cancer, Disease and Developmental Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Boris NovakovicDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Cancer, Disease and Developmental Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Xin LiEarly Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Blaise WeinrichEarly Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Nicole CarsonEarly Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Miina OllikainenHjelt Institute; Department of Public Health; University of Helsinki; Helsinki, Finland.
Hong-Kiat NgCancer, Disease and Developmental Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Roberta AndronikosDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Early Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Nur Khairunnisa Abdul AzizDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Early Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Richard SafferyDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Cancer, Disease and Developmental Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Jeffrey M CraigDepartment of Paediatrics; University of Melbourne; Parkville, VIC Australia; Early Life Epigenetics Group; Murdoch Childrens Research Institute (MCRI); Royal Children's Hospital; Parkville, VIC Australia.
Royal Children's Hospital · AUUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetic events are crucial for early development, but can be influenced by environmental factors, potentially programming the genome for later adverse health outcomes. The insulin-like growth factor 2 (IGF2)/H19 locus is crucial for prenatal growth and the epigenetic state at this locus is environmentally labile. Recent studies have implicated maternal factors, including folate intake and smoking, in the regulation of DNA methylation at this locus, although data are often conflicting in the direction and magnitude of effect. Most studies have focused on single tissues and on one or two differentially-methylated regions (DMRs) regulating IGF2/H19 expression. In this study, we investigated the relationship between multiple shared and non-shared gestational/maternal factors and DNA methylation at four IGF2/H19 DMRs in five newborn cell types from 67 pairs of monozygotic and 49 pairs of dizygotic twins. Data on maternal and non-shared supply line factors were collected during the second and third trimesters of pregnancy and DNA methylation was measured via mass spectrometry using Sequenom MassArray EpiTyper analysis. Our exploratory approach showed that the site of umbilical cord insertion into the placenta in monochorionic twins has the strongest positive association with methylation in all IGF2/H19 DMRs (p<0.05). Further, evidence for tissue- and locus-specific effects were observed, emphasizing that responsiveness to environmental exposures in utero cannot be generalized across genes and tissues, potentially accounting for the lack of consistency in previous findings. Such complexity in responsiveness to environmental exposures in utero has implications for all epigenetic studies investigating the developmental origins of health and disease.

Indexed as

DNA MethylationGenetic LociGenomic ImprintingPrenatal Nutritional Physiological PhenomenaDiabetes, GestationalFemaleHumansInfant, NewbornInsulin-Like Growth Factor IIMaleOrgan SpecificityPregnancyRNA, Long NoncodingTwins, DizygoticTwins, MonozygoticH19 long non-coding RNAIGF2 protein, humanInsulin-Like Growth Factor IIRNA, Long Noncodingdevelopmental origins of health and disease (DOHaD)DNA methylationimprinted genesmaternal factorstwins

Identifiers

PMID23917818
PMCPMC3891688
OpenAlexW2061004417

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.