Evidence map›Paper›PMID 24767625›Full record

ArticlePsychoneuroendocrinology2014

Alterations in DNA methylation of Fkbp5 as a determinant of blood-brain correlation of glucocorticoid exposure.

Erin R Ewald, Gary S Wand, Fayaz Seifuddin, Xiaoju Yang, Kellie L Tamashiro, James B Potash, Peter Zandi, Richard S Lee

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. A randomized, double-blind, placebo-controlled trial of lamotrigine for prescription corticosteroid effects on the human hippocampus.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2019
    Trial
  3. Trial
  4. The relationship between childhood trauma, rs1360780 genotypes,European journal of psychotraumatology · 2025
    Article
  5. Article
  6. Article
  7. Blood DNA methylation ofFrontiers in epigenetics and epigenomics · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
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  20. Glucocorticoid exposure during hippocampal neurogenesis primes future stress response by inducing changes in DNA methylation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

8 authors at 3 institutions in 1 country.

Erin R EwaldJohns Hopkins Mood Disorders Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Gary S WandDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Division of Endocrinology of the Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Fayaz SeifuddinJohns Hopkins Mood Disorders Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Xiaoju YangDivision of Endocrinology of the Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Kellie L TamashiroJohns Hopkins Mood Disorders Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
James B PotashDepartment of Psychiatry, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.
Peter ZandiJohns Hopkins Mood Disorders Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Mental Health of the Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA.
Richard S LeeJohns Hopkins Mood Disorders Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. Electronic address: richardlee@jhmi.edu.
Johns Hopkins University · USJohns Hopkins Medicine · USUniversity of Iowa Hospitals and Clinics · US

Funding

Stress Effects on Alcohol Consumption: Age of onset and genes in heavy drinkersU01AA020890 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI MCCAUL, MARY E, WAND, GARY S · 2012 to 2021
$3.6M
Neuroendocrine Investigators and Mentoring in the field of Alcohol ResearchK05AA020342 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI WAND, GARY S · 2011 to 2015
$872k
Influences of the prenatal environment on metabolic programmingR00HD055030 · NICHD · JOHNS HOPKINS UNIVERSITY · PI TAMASHIRO, KELLIE L. K. · 2009 to 2011
$782k
Influences of the prenatal environment on metabolic programmingK99HD055030 · NICHD · JOHNS HOPKINS UNIVERSITY · PI TAMASHIRO, KELLIE L. K. · 2007 to 2008
$135k
NIAAA NIH HHS K05 AA020342NIAAA NIH HHS U01 AA020890NIAAA NIH HHS UO1 AA020890NICHD NIH HHS HD055030NICHD NIH HHS K99 HD055030NICHD NIH HHS R00 HD055030
6 · The paper itself

Abstract

backgroundEpigenetic studies that utilize peripheral tissues to identify molecular substrates of neuropsychiatric disorders rely on the assumption that disease-relevant, cellular alterations that occur in the brain are mirrored and detectable in peripheral tissues such as blood. We sought to test this assumption by using a mouse model of Cushing's disease and asking whether epigenetic changes induced by glucocorticoids can be correlated between these tissue types.

methodsMice were treated with different doses of glucocorticoids in their drinking water for four weeks to assess gene expression and DNA methylation (DNAm) changes in the stress response gene Fkbp5.

resultsSignificant linear relationships were observed between DNAm and four-week mean plasma corticosterone levels for both blood (R(2)=0.68, P=7.1×10(-10)) and brain (R(2)=0.33, P=0.001). Further, degree of methylation change in blood correlated significantly with both methylation (R(2)=0.49, P=2.7×10(-5)) and expression (R(2)=0.43, P=3.5×10(-5)) changes in hippocampus, with the notable observation that methylation changes occurred at different intronic regions between blood and brain tissues.

conclusionAlthough our findings are limited to several intronic CpGs in a single gene, our results demonstrate that DNA from blood can be used to assess dynamic, glucocorticoid-induced changes occurring in the brain. However, for such correlation analyses to be effective, tissue-specific locations of these epigenetic changes may need to be considered when investigating brain-relevant changes in peripheral tissues.

Indexed as

AnimalsBrainCorticosteroneDNA MethylationGlucocorticoidsMaleMiceMice, Inbred C57BLTacrolimus Binding Protein 5Tacrolimus Binding ProteinsCorticosteroneGlucocorticoidsTacrolimus Binding Protein 5Tacrolimus Binding Proteinsand GlucocorticoidsBiomarkerBlood–brain correlationDNA methylationEpigeneticsFkbp5

Identifiers

PMID24767625
PMCPMC4047971
OpenAlexW2117041810

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.