Evidence map›Paper›PMID 22202639›Full record

ArticleGene2012

Gender-specific methylation differences in relation to prenatal exposure to cigarette smoke.

Susan K Murphy, Abayomi Adigun, Zhiqing Huang, Francine Overcash, Frances Wang, Randy L Jirtle, Joellen M Schildkraut, Amy P Murtha, Edwin S Iversen, Cathrine Hoyo

Abstract read
In one paragraph

Article in Gene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
27.1field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 231 citations in OpenAlex.

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  15. Early Life Programming of Skeletal Health.Current osteoporosis reports · 2023
    Review
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81 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Susan K MurphyDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University Medical Center, Durham, NC 27708, USA. susan.murphy@duke.edu
Abayomi Adigun
Zhiqing Huang
Francine Overcash
Frances Wang
Randy L Jirtle
Joellen M Schildkraut
Amy P Murtha
Edwin S Iversen
Cathrine Hoyo
Duke Medical Center · USDuke University Hospital · USDuke University · US

Funding

Nutrition, Deregulation of Imprinted GenesR01ES016772 · NIEHS · DUKE UNIVERSITY · PI HOYO, CATHRINE · 2009 to 2013
$3.1M
Obesity and deregulation of imprinted genes in early lifeR01DK085173 · NIDDK · DUKE UNIVERSITY · PI HOYO, CATHRINE, MURPHY, SUSAN KAY · 2010 to 2013
$2.3M
In-utero Exposure and Infant Loss of IGF2 ImprintingR21ES014947 · NIEHS · DUKE UNIVERSITY · PI HOYO, CATHRINE · 2006 to 2007
$384k
NIDDK NIH HHS R01 DK085173NIDDK NIH HHS R01DK085173NIEHS NIH HHS R01 ES016772NIEHS NIH HHS R01ES016772NIEHS NIH HHS R21 ES014947NIEHS NIH HHS R21ES014947
6 · The paper itself

Abstract

Epigenetic alterations may mechanistically explain the developmental origins of adult disease, namely the hypothesis that many complex adult chronic diseases originate as a result of conditions encountered in utero. If true, epigenetically regulated imprinted genes, critical to normal growth and development, may partially mediate these outcomes. We determined the influence of in utero exposure to cigarette smoking on methylation at two differentially methylated regions (DMRs) regulating Insulin-like Growth Factor 2 (IGF2) and H19, and how this might relate to birth weight of infants born to 418 pregnant women. Smoking status was ascertained through self-report and medical records. Bisulfite pyrosequencing was used to measure methylation in umbilical cord blood DNAs. Least squares DNA methylation means at each DMR and birth weight were compared between infants of smokers and non-smokers, using generalized linear models. While there were no significant differences at the H19 DMR, infants born to smokers had higher methylation at the IGF2 DMR than those born to never smokers or those who quit during pregnancy (49.5%, SD=8.0 versus 46.6%, SD=5.6 and 45.8%, SD=6.3, respectively; p=0.0002). The smoking-related increase in methylation was most pronounced in male offspring (p for sex interaction=0.03), for whom approximately 20% of smoking-related low birth weight was mediated by DNA methylation at the IGF2 DMR. Our findings suggest that IGF2 DMR plasticity is an important mechanism by which in utero adjustments to environmental toxicants are conferred. Larger studies to replicate these findings are required.

Indexed as

DNA MethylationGenomic ImprintingMaternal-Fetal ExchangeRNA, UntranslatedSex CharacteristicsAdultBirth WeightFemaleFetal BloodHumansInsulin-Like Growth Factor IIMalePregnancyRNA, Long NoncodingSmokingH19 long non-coding RNAInsulin-Like Growth Factor IIRNA, Long NoncodingRNA, Untranslated

Identifiers

PMID22202639
PMCPMC3627389
OpenAlexW2003006766

What OpenQuestion 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 OpenQuestion graph.