Evidence map›Paper›PMID 25742137›Full record

ArticlePloS one2015

Ancestry dependent DNA methylation and influence of maternal nutrition.

Khyobeni Mozhui, Alicia K Smith, Frances A Tylavsky

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.5field-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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  9. A biosocial return to race? A cautionary view for the postgenomic era.American journal of human biology : the official journal of the Human Biology Council · 2022
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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

3 authors at 2 institutions in 1 country.

Khyobeni MozhuiDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, United States of America.
Alicia K SmithDepartment of Psychiatry and Behavioral Science, Emory University, Atlanta, GA, United States of America.
Frances A TylavskyDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, United States of America.
University of Tennessee Health Science Center · USEmory University · US

Funding

USE OF MOTIVATIONAL INTERVIEWING TO MANAGE TYPE I DIABETESM01RR000211 · NCRR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DAGOGO-JACK, SAMUEL · 1985 to 2006
$9.6M
Pregnancy Folate Status & Early Childhood Respiratory & Atopic Disease OutcomesR01HL109977 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CARROLL, KECIA NICOLE · 2011 to 2015
$3.4M
Epigenetic and Biobehavioral Determinants of Preterm Birth in Black WomenR01MD009064 · NIMHD · EMORY UNIVERSITY · PI DUNLOP, ANNE LANG, SMITH, ALICIA K · 2014 to 2018
$1.9M
Genomics and Epigenomics of Fetal Growth RegulationR01HD060713 · NICHD · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TYLAVSKY, FRANCES A · 2009 to 2010
$1.3M
Maternal-Fetal Conflict: The Effect of Imprinted Genes on Fetal GrowthR01HD055462 · NICHD · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TYLAVSKY, FRANCES A · 2007 to 2010
$1.1M
NCRR NIH HHS M01 RR000211NCRR NIH HHS M01-RR00211NHLBI NIH HHS 1R01HL109977NHLBI NIH HHS R01 HL109977NICHD NIH HHS HD055462NICHD NIH HHS HD060713NICHD NIH HHS R01 HD055462NICHD NIH HHS R01 HD060713NIMHD NIH HHS R01 MD009064NIMHD NIH HHS R01MD009064
6 · The paper itself

Abstract

There is extensive variation in DNA methylation between individuals and ethnic groups. These differences arise from a combination of genetic and non-genetic influences and potential modifiers include nutritional cues, early life experience, and social and physical environments. Here we compare genome-wide DNA methylation in neonatal cord blood from African American (AA; N = 112) and European American (EA; N = 91) participants of the CANDLE Study (Conditions Affecting Neurocognitive Development and Learning in Early Childhood). Our goal is to determine if there are replicable ancestry-specific methylation patterns that may implicate risk factors for diseases that have differential prevalence between populations. To identify the most robust ancestry-specific CpG sites, we replicate our results in lymphoblastoid cell lines from Yoruba African and CEPH European panels of HapMap. We also evaluate the influence of maternal nutrition--specifically, plasma levels of vitamin D and folate during pregnancy--on methylation in newborns. We define stable ancestry-dependent methylation of genes that include tumor suppressors and cell cycle regulators (e.g., APC, BRCA1, MCC). Overall, there is lower global methylation in African ancestral groups. Plasma levels of 25-hydroxy vitamin D are also considerably lower among AA mothers and about 60% of AA and 40% of EA mothers have concentrations below 20 ng/ml. Using a weighted correlation analysis, we define a network of CpG sites that is jointly modulated by ancestry and maternal vitamin D. Our results show that differences in DNA methylation patterns are remarkably stable and maternal micronutrients can exert an influence on the child epigenome.

Indexed as

CpG IslandsDNA MethylationGenetic Predisposition to DiseaseMaternal Nutritional Physiological PhenomenaAdolescentAdultBlack or African AmericanBlack PeopleEpigenesis, GeneticFemaleFetal BloodGene-Environment InteractionGenome-Wide Association StudyHumansInfant, NewbornMale

Identifiers

PMID25742137
PMCPMC4350920
OpenAlexW2109505394

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.