Evidence map›Paper›PMID 25945130›Full record

ArticleClinical epigenetics2015

Racial differences in IGF1 methylation and birth weight.

Jennifer K Straughen, Levent Sipahi, Monica Uddin, Dawn P Misra, Vinod K Misra

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. DNA methylation-based variation between human populations.Molecular genetics and genomics : MGG · 2017
    Review
  10. 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

5 authors at 2 institutions in 1 country.

Jennifer K StraughenDepartment of Family Medicine and Public Health Sciences, The Wayne State University School of Medicine, 3939 Woodward Avenue, Detroit, MI 48201 USA ; Current address: Department of Public Health Sciences, Henry Ford Hospital, One Ford Place, Detroit, MI 48202 USA.
Levent SipahiCenter for Molecular Medicine and Genetics, The Wayne State University School of Medicine, 540 East Canfield, Detroit, MI 48201 USA.
Monica UddinDepartment of Psychology, University of Illinois at Urbana-Champaign, 603 E. Daniel Street, Champaign, IL 61820 USA.
Dawn P MisraDepartment of Family Medicine and Public Health Sciences, The Wayne State University School of Medicine, 3939 Woodward Avenue, Detroit, MI 48201 USA.
Vinod K MisraDepartment of Pediatrics, Division of Genetic and Metabolic Disorders, The Wayne State University School of Medicine, 3901 Beaubien Blvd, Detroit, MI 48201 USA ; Children's Hospital of Michigan, Division of Genetic and Metabolic Disorders, The Wayne State University School of Medicine, 3950 Beaubien Blvd, Detroit, MI 48201 USA.
Wayne State University · USUniversity of Illinois Urbana-Champaign · US

Funding

NCCDPHP CDC HHS R36 DP001898
6 · The paper itself

Abstract

backgroundThe birth weight of Black neonates in the United States is consistently smaller than that of their White counterparts. Epigenetic differences between the races may be involved in such disparities. The goal of these analyses was to model the role of IGF1 methylation in mediating the association between race and birth weight. Data was collected on a cohort of 87 live born infants. IGF1 methylation was measured in DNA isolated from the mononuclear fraction of umbilical cord blood collected after delivery. Quantitative, loci-specific methylation was assessed using the Infinium HumanMethylation27 BeadArray (Illumina Inc., San Diego, CA). Locus specific methylation of the IGF1 CpG site was validated on a subset of the original sample (N = 61) using pyrosequencing. Multiple linear regression was used to examine relationships between IGF1 methylation, race, and birth weight. A formal mediation analysis was then used to estimate the relationship of IGF1 methylation to race and birth weight.

resultsBlack race was associated with a 7.45% decrease in gestational age-adjusted birth weight (aBW) (P = 0.04) and Black infants had significantly higher IGF1 methylation than non-Black infants (P < 0.05). A one standard deviation increase in IGF1 methylation was associated with a 3.32% decrease in aBW (P = 0.02). Including IGF1 methylation as a covariate, the effect of Black race on aBW was attenuated. A formal mediation analysis showed that the controlled direct effect of Black race on aBW was -6.26% (95% CI = -14.15, 1.06); the total effect of Black race on IGF1 methylation was -8.12% (95% CI = -16.08, -0.55); and the natural indirect effect of Black race on aBW through IGF1 methylation was -1.86% (95% CI = -5.22, 0.18).

conclusionThe results of the mediation analysis along with the multivariable regression analyses suggest that IGF1 methylation may partially mediate the relationship between Black race and aBW. Such epigenetic differences may be involved in racial disparities observed in perinatal outcomes.

Indexed as

Birth weightDisparitiesEpigeneticsIGF1MethylationPerinatalRace

Identifiers

PMID25945130
PMCPMC4419394
OpenAlexW2070976254

What OpenQuestion holds

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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.