Evidence map›Paper›PMID 22119400›Full record

Trial reportBrain, behavior, and immunity2012

Maintenance of a positive outlook during acute stress protects against pro-inflammatory reactivity and future depressive symptoms.

K Aschbacher, E Epel, O M Wolkowitz, A A Prather, E Puterman, F S Dhabhar

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Brain, behavior, and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 22% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
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  10. Associations between emotion reactivity to daily interpersonal stress and acute social-evaluative stress during late adolescence.Stress and health : journal of the International Society for the Investigation of Stress · 2024
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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

6 authors at 2 institutions in 1 country.

K AschbacherDepartment of Psychiatry, School of Medicine, University of California San Francisco, CA 94143-0848, USA. kirstin.aschbacher@ucsf.edu
E Epel
O M Wolkowitz
A A Prather
E Puterman
F S Dhabhar
University of California, San Francisco · USStanford University · US

Funding

Chronic and Acute Psychosocial Stress and Impaired Cell AgingR01AG030424 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EPEL, ELISSA S. · 2010 to 2014
$3.5M
Effects of Psychosocial Stress on Endothelial Progenitor CellsK23HL112955 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ASCHBACHER, KIRSTIN · 2012 to 2015
$575k
NHLBI NIH HHS K23 HL112955NIA NIH HHS R01 AG030424NIA NIH HHS R01 AG030424-01A2
6 · The paper itself

Abstract

unlabelledCognitive and affective responses to acute stress influence pro-inflammatory cytokine reactivity, and peripheral cytokines (particularly interleukin-1 beta (IL-1β)), can act on the brain to promote depressive symptoms. It is unknown whether acute stress-induced changes in positive affect and cognitions (POS) and pro-inflammatory reactivity predict future depressive symptoms. We examined acute stress responses among women, to determine prospective predictors of depressive symptoms. HYPOTHESES: (1) Stress-induced decreases in POS will be associated with stress-related increases in circulating IL-1β. (2) Acute stress-induced decreases in POS and increases in IL-1β reactivity will predict increases in depressive symptoms 1 year later. Thirty-five post-menopausal women were exposed to acute stress with the Trier Social Stress Task (TSST) and provided blood samples under resting conditions and 30 min after the conclusion of the TSST, which were assayed for IL-1β. IL-1β reactivity was quantified as post minus pre-TSST. Failure to maintain POS was quantified as the decrease in POS during the TSST. Change in depressive symptoms from the study baseline to the following year was determined. Greater acute stress-induced declines in POS were significantly associated with increased IL-1β reactivity (p≤.02), which significantly predicted increases in depressive symptoms over the following year (p<.01), controlling for age, body mass index, chronic stress, antidepressant use and baseline depressive symptoms. IL-1β reactivity was a significant mediator of the relationship between POS decline and future increases in depressive symptoms (p=.04). Difficulty maintaining positivity under stress and heightened pro-inflammatory reactivity may be markers and/or mechanisms of risk for future increases in depressive symptoms.

Indexed as

AffectAgedDepressionFemaleHumansInflammationInterleukin-1betaInterleukin-6Middle AgedPsychiatric Status Rating ScalesStress, PsychologicalTime FactorsInterleukin-1betaInterleukin-6

Identifiers

PMID22119400
PMCPMC4030538
OpenAlexW2015010043

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.