Evidence map›Paper›PMID 33452438›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2021

Beta-adrenergic blockade blunts inflammatory and antiviral/antibody gene expression responses to acute psychosocial stress.

Jennifer K MacCormack, Monica M Gaudier-Diaz, Emma L Armstrong-Carter, Jesusa M G Arevalo, Samantha Meltzer-Brody, Erica K Sloan, Steven W Cole, Keely A Muscatell

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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

22 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Social Genomic Determinants of Health: Understanding the Molecular Pathways by Which Neighborhood Disadvantage Affects Cancer Outcomes.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Support-Giving Is Associated With Lower Systemic Inflammation.Annals of behavioral medicine : a publication of the Society of Behavioral Medicine · 2023
    Article
  15. Article
  16. Article
  17. Brain-body pathways linking racism and health.The American psychologist · 2022
    Article
  18. Review
  19. Article
  20. Review
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.

Jennifer K MacCormackDepartment of Psychology & Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. maccormack@pitt.edu.ORCID http://orcid.org/0000-0002-1199-0121
Monica M Gaudier-DiazDepartment of Psychology & Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Emma L Armstrong-CarterGraduate School of Education, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-5847-9486
Jesusa M G ArevaloDepartment of Medicine, Division of Hematology-Oncology, University of California, Los Angeles, CA, USA.
Samantha Meltzer-BrodyDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Erica K SloanMonash Institute of Pharmaceutical Sciences, Drug Discovery Biology Theme, Monash University, Parkville, VIC, Australia.
Steven W ColeDepartment of Medicine, Division of Hematology-Oncology, University of California, Los Angeles, CA, USA.
Keely A MuscatellDepartment of Psychology & Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID http://orcid.org/0000-0002-7893-5565

Funding

Re-Entry Supplement: Investigation of Oral Microbial Enzymes for the Detection and Treatment of Periodontal DiseaseUL1TR002489 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, SHAHEEN, NICHOLAS J · 2018 to 2022
$48.6M
USC/UCLA Center on Biodemography &Population HealthP30AG017265 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE, HIRAM BELTRAN-SANCHEZ · 1999 to 2026
$17.9M
CARDIOVASCULAR BEHAVIORAL MEDICINE RESEARCH TRAININGT32HL007560 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Peter J Gianaros, REBECCA C THURSTON · 1985 to 2026
$11.3M
Neural Contributions to Older Adults Embodied Emotion Experience and RegulationF31AG055265 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MACCORMACK, JENNIFER KAY · 2017 to 2019
$72k
NCATS NIH HHS UL1 TR002489NHLBI NIH HHS T32 HL007560NIA NIH HHS F31 AG055265NIA NIH HHS P30 AG017265
6 · The paper itself

Abstract

Dysregulation of the immune system is one potential mechanism by which acute stress may contribute to downstream disease etiology and psychopathology. Here, we tested the role of β-adrenergic signaling as a mediator of acute stress-induced changes in immune cell gene expression. In a randomized, double-blind, and placebo-controlled trial, 90 healthy young adults (44% female) received a single 40 mg dose of the β-blocker propranolol (n = 43) or a placebo (n = 47) and then completed the Trier Social Stress Test (TSST). Pre- and post-stress blood samples were assayed for prespecified sets of pro-inflammatory and antiviral/antibody gene transcripts. Analyses revealed increased expression of both inflammatory and antiviral/antibody-related genes in response to the TSST, and these effects were blocked by pre-treatment with propranolol. Bioinformatics identified natural killer cells and dendritic cells as the primary cellular context for transcriptional upregulation, and monocytes as the primary cellular carrier of genes downregulated by the TSST. These effects were in part explained by acute changes in circulating cell types. Results suggest that acute psychosocial stress can induce an "acute defense" molecular phenotype via β-adrenergic signaling that involves mobilization of natural killer cells and dendritic cells at the expense of monocytes. This may represent an adaptive response to the risk of acute injury. These findings offer some of the first evidence in humans that β-blockade attenuates psychosocial stress-induced increases in inflammatory gene expression, offering new insights into the molecular and immunologic pathways by which stress may confer risks to health and well-being.

Indexed as

Adrenergic beta-AntagonistsAntiviral AgentsFemaleGene ExpressionHumansHydrocortisoneMalePropranololStress, PsychologicalYoung AdultAdrenergic beta-AntagonistsAntiviral AgentsHydrocortisonePropranolol

Identifiers

PMID33452438
PMCPMC8027189

What OpenQuestion holds

Textmetadata
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.