Evidence map›Paper›PMID 21600281›Full record

ArticleBrain, behavior, and immunity2011

DNA methylation as a risk factor in the effects of early life stress.

Erin L Kinnally, Caroline Feinberg, David Kim, Kerel Ferguson, Rudolph Leibel, Jeremy D Coplan, J John Mann

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
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  14. Effect of Early Life Stress on the Epigenetic Profiles in Depression.Frontiers in cell and developmental biology · 2020
    Review
  15. Article
  16. Review
  17. Article
  18. Epigenetic Landscapes of the Adversity-Exposed Brain.Progress in molecular biology and translational science · 2018
    Review
  19. Review
  20. Early rearing history influences oxytocin receptor epigenetic regulation in rhesus macaques.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

7 authors at 2 institutions in 1 country.

Erin L KinnallyDepartment of Psychiatry, Columbia University, 1051 Riverside Drive, New York, NY 10032, United States. ek2500@columbia.edu
Caroline Feinberg
David Kim
Kerel Ferguson
Rudolph Leibel
Jeremy D Coplan
J John Mann
SUNY Downstate Health Sciences University · USColumbia University · US

Funding

THE NEUROBIOLOGY OF SUICIDAL BEHAVIORP50MH062185 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI MANN, JOSEPH JOHN · 2000 to 2009
$21.7M
Translational Neuroscience Training Grant.T32MH015174 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DENNY, CHRISTINE ANN · 1985 to 2020
$4.0M
ADVERSE EARLY REARING &GLUTAMATERGIC FUNCTIONR01MH059990 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI COPLAN, JEREMY D · 2000 to 2003
$1.1M
NIMH NIH HHS 1R01MH059990-01A1NIMH NIH HHS 5T32MH015174NIMH NIH HHS P50 MH062185NIMH NIH HHS R01 MH059990NIMH NIH HHS T32 MH015174
6 · The paper itself

Abstract

Epigenetic marks (e.g., DNA 5-methylcytosine [5mC] content or CpG methylation) within specific gene regulatory regions have been demonstrated to play diverse roles in stress adaptation and resulting health trajectories following early adversity. Yet the developmental programming of the vast majority of the epigenome has not yet been characterized, and its role in the impact of early stress largely unknown. In the present study, we investigated the relationships among early life stress, whole-epigenome and candidate stress pathway gene (serotonin transporter, 5-HTT) methylation patterns, and adult behavioral stress adaptation in a non-human primate model. Early in life, experimental variable foraging demand (VFD) stress or control conditions were administered to two groups each of 10 female bonnet macaques (Macaca radiata) and their mothers. As adults (3-13 years of age), these females were assessed for behavioral adaptation to stress across four conditions of increasing intensity. Blood DNA 5-HTT 5mC status was determined using sodium bisulfite pyrosequencing and total 5mC content was determined using ELISA. Neither stress reactivity nor DNA methylation differed based on early life stress. However, we found that both greater 5-HTT and whole-genome 5mC was associated with enhanced behavioral stress reactivity following early life stress, but not control conditions. Therefore, regardless of developmental origin, greater DNA methylation conferred a genomic background of "risk" in the context of early stress. We suggest that this may arise from constrained plasticity in gene expression needed for stress adaptation early in development. This risk may have wider implications for psychological and physical stress adaptation and health.

Indexed as

Adaptation, PsychologicalAnimalsDNA MethylationExtinction, PsychologicalFactor Analysis, StatisticalFearFeeding BehaviorFemaleMacaca radiataMaternal BehaviorMiceRisk FactorsSequence Analysis, DNASerotonin Plasma Membrane Transport ProteinsStress, PsychologicalSulfitesSerotonin Plasma Membrane Transport Proteinssodium bisulfiteSulfites

Identifiers

PMID21600281
PMCPMC3191272
OpenAlexW2080712930

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.