Evidence map›Paper›PMID 29162190›Full record

ArticleDevelopment and psychopathology2017

Early life stress, FK506 binding protein 5 gene (FKBP5) methylation, and inhibition-related prefrontal function: A prospective longitudinal study.

Madeline B Harms, Rasmus Birn, Nadine Provencal, Tobias Wiechmann, Elisabeth B Binder, Sebastian W Giakas, Barbara J Roeber, Seth D Pollak

Abstract read
In one paragraph

Article in Development and psychopathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  15. Age-related no-go P300 amplitudes are moderated by exposure to early-life stress.International journal of psychophysiology : official journal of the International Organization of Psychophysiology · 2022
    Article
  16. Association Between Childhood Maltreatment,Frontiers in psychiatry · 2022
    Article
  17. Review
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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

8 authors.

Madeline B HarmsUniversity of Wisconsin-Madison.
Rasmus BirnUniversity of Wisconsin-Madison.
Nadine ProvencalMax Planck Institute of Psychiatry.
Tobias WiechmannMax Planck Institute of Psychiatry.
Elisabeth B BinderMax Planck Institute of Psychiatry.
Sebastian W GiakasUniversity of Wisconsin-Madison.
Barbara J RoeberUniversity of Wisconsin-Madison.
Seth D PollakUniversity of Wisconsin-Madison.

Funding

WISCONSIN CENTER ON MENTAL RETARDATION: CORE SUPPORTP30HD003352 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI MESSING, ALBEE · 1985 to 2015
$25.2M
Emotion Processing:Risk for Psychopathology in ChildrenR01MH061285 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI SETH D POLLAK · 2001 to 2026
$12.4M
TRAINING PROGRAM IN EMOTION RESEARCHT32MH018931 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Richard J Davidson · 1989 to 2026
$11.6M
NICHD NIH HHS P30 HD003352NIMH NIH HHS R01 MH061285NIMH NIH HHS T32 MH018931
6 · The paper itself

Abstract

Individuals who have experienced high levels of childhood stress are at increased risk for a wide range of behavioral problems that persist into adulthood, yet the neurobiological and molecular mechanisms underlying these associations remain poorly understood. Many of the difficulties observed in stress-exposed children involve problems with learning and inhibitory control. This experiment was designed to test individuals' ability to learn to inhibit responding during a laboratory task. To do so, we measured stress exposure among a community sample of school-aged children, and then followed these children for a decade. Those from the highest and lowest quintiles of childhood stress exposure were invited to return to our laboratory as young adults. At that time, we reassessed their life stress exposure, acquired functional magnetic resonance imaging data during an inhibitory control task, and assayed these individuals' levels of methylation in the FK506 binding protein 5 (FKBP5) gene. We found that individuals who experienced high levels of stress in childhood showed less differentiation in the dorsolateral prefrontal cortex between error and correct trials during inhibition. This effect was associated only with childhood stress exposure and not by current levels of stress in adulthood. In addition, FKBP5 methylation mediated the association between early life stress and inhibition-related prefrontal activity. These findings are discussed in terms of using multiple levels of analyses to understand the ways in which adversity in early development may affect adult behavioral adaptation.

Indexed as

DNA MethylationLife Change EventsNeural InhibitionAdolescentAdult Survivors of Child Adverse EventsChildFemaleFunctional NeuroimagingHumansLongitudinal StudiesMagnetic Resonance ImagingMalePrefrontal CortexProspective StudiesRiskStress, PsychologicalTacrolimus Binding Protein 5Tacrolimus Binding Proteins

Identifiers

PMID29162190
PMCPMC5726293

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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.