Evidence map›Paper›PMID 32243432›Full record

ArticlePloS one2020

Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study.

Idan Shalev, Waylon J Hastings, Laura Etzel, Salomon Israel, Michael A Russell, Kelsie A Hendrick, Megan Zinobile, Sue Rutherford Siegel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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 at 2 institutions in 2 countries.

Idan ShalevDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.ORCID 0000-0003-0773-4835
Waylon J HastingsDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Laura EtzelDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Salomon IsraelDepartment of Psychology, The Hebrew University of Jerusalem, Jerusalem, Israel.
Michael A RussellDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Kelsie A HendrickDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Megan ZinobileDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Sue Rutherford SiegelDepartment of Biobehavioral Health, The Pennsylvania State University, University Park, PA, United States of America.
Pennsylvania State University · USHebrew University of Jerusalem · IL

Funding

Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
Psychosocial Determinants and Biological Pathway to Healthy Aging (Pathways)T32AG049676 · NIA · PENNSYLVANIA STATE UNIVERSITY, THE · PI LYNN M. MARTIRE · 2016 to 2026
$3.9M
A pilot study to advance translation of molecular signatures of biological agingR21AG054846 · NIA · DUKE UNIVERSITY · PI BELSKY, DANIEL WALKER · 2017 to 2018
$437k
Temporal Genomics Mechanisms Underlying Disease and AgingR21AG055621 · NIA · PENNSYLVANIA STATE UNIVERSITY, THE · PI SHALEV, IDAN · 2018 to 2019
$436k
NCATS NIH HHS UL1 TR002014NIA NIH HHS R21 AG054846NIA NIH HHS R21 AG055621NIA NIH HHS T32 AG049676
6 · The paper itself

Abstract

objectiveExposure to early-life adversity (ELA) can result in long-term changes to physiological systems, which predispose individuals to negative health outcomes. This biological embedding of stress-responsive systems may operate via dysregulation of physiological resources in response to common stressors. The present pilot study outlines a novel experimental design to test how young adults' exposure to ELA influences neuroendocrine and inflammatory responses to acute stress. MATERIALS AND

methodsParticipants were 12 males (mean age = 21.25), half of whom endorsed at least three significant adverse events up to age 18 years ('ELA group'), and half who confirmed zero ('controls'). Using a randomized within-subjects, between-groups experimental design, we induced acute psychosocial stress (Trier Social Stress Test, TSST), and included a no-stress control condition one week apart. During these sessions, we obtained repeated measurements of physiological reactivity, gene expression of the glucocorticoid receptor (NR3C1), and plasma levels of pro-inflammatory cytokines (IL-1β, IL-6, IL-8 and TNFα) over a 4-hour window post-test.

resultsIn this pilot study, the ELA group evinced higher cortisol response and blunted NR3C1 gene expression in response to the TSST compared with controls, while no differences were observed in the no-stress condition. For pro-inflammatory cytokines, only IL-6 increased significantly in response to the TSST, with no differences between the two groups.

conclusionOverall, this pilot feasibility study provides a framework to investigate the biological embedding of early-adversity via dysregulation across physiological and genomic systems in response to acute psychosocial stress. ELA may program such systems in a maladaptive manner more likely to manifest during times of duress, predisposing individuals to the negative health consequences of everyday stressors. Future studies with larger sample size including both males and females are needed to replicate and expand upon these preliminary findings.

Indexed as

AdolescentAdultCytokinesFeasibility StudiesFemaleGene Expression RegulationHumansImmunityMalePilot ProjectsReceptors, GlucocorticoidStress, PsychologicalYoung AdultCytokinesNR3C1 protein, humanReceptors, Glucocorticoid

Identifiers

PMID32243432
PMCPMC7122782
OpenAlexW3014935908

What OpenQuestion holds

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LicenceCC BY
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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.