Evidence map›Paper›PMID 30822466›Full record

ArticleBrain, behavior, and immunity2020

Longitudinal changes of inflammatory biomarkers moderate the relationship between recent stressful life events and prospective symptoms of depression in a diverse sample of urban adolescents.

Marin M Kautz, Christopher L Coe, Brae Anne McArthur, Naoise Mac Giollabhui, Lauren M Ellman, Lyn Y Abramson, Lauren B Alloy

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.3field-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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  11. Biomarkers of Stress and Inflammation in Children.Biological research for nursing · 2023
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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

7 authors at 2 institutions in 1 country.

Marin M KautzDepartment of Psychology, Temple University, United States.
Christopher L CoeDepartment of Psychology, University of Wisconsin-Madison, United States.
Brae Anne McArthurDepartment of Psychology, Temple University, United States.
Naoise Mac GiollabhuiDepartment of Psychology, Temple University, United States.
Lauren M EllmanDepartment of Psychology, Temple University, United States.
Lyn Y AbramsonDepartment of Psychology, University of Wisconsin-Madison, United States.
Lauren B AlloyDepartment of Psychology, Temple University, United States. Electronic address: lalloy@temple.edu.
Temple University · USUniversity of Wisconsin–Madison · US

Funding

Depression Surge in Adolescence & Gender Differences: Biocognitive MechanismsR01MH079369 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ABRAMSON, LYN Y, ALLOY, LAUREN BERSH · 2008 to 2012
$3.4M
Risk for Adolescent Depression: Stress, Cognitive Vulnerability, & InflammationR01MH101168 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI ALLOY, LAUREN BERSH · 2013 to 2017
$3.2M
Chronic Inflammation as a Pathway to Cognitive Dysfunction in Adolescents and Young Adults with a History of Elevated Depressive SymptomsF31MH118808 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI MAC GIOLLABHUI, NAOISE · 2019 to 2020
$67k
NIMH NIH HHS F31 MH118808NIMH NIH HHS R01 MH079369NIMH NIH HHS R01 MH101168
6 · The paper itself

Abstract

This study investigated whether longitudinal changes in inflammatory physiology moderated the relationship between recent stressful life events and subsequent depressive symptoms in adolescence. A diverse sample of adolescents representative of an urban community (N = 129; Age at baseline = 12.5 years; 48.8% female; 55.0% African American) completed measures of stressful life events, depressive symptoms, and two annual blood draws (BD1 and BD2). Controlling for inflammatory activity at BD1, depression at BD1, demographics and the time between assessments, increases in interleukin-6 (IL-6; b = 0.878, p = .007) and C-reactive protein (CRP; b = 0.252, p = .024) from BD1 to BD2 interacted with recent stressful life events before BD1 to predict severity of depressive symptoms at BD2. Similar associations were evident for IL-6 (b = 2.074, p = .040) and CRP (b = 0.919, p = .050) when considering acute stressful life events that had occurred within the two weeks before the first blood collection. More frequent stressful life events before BD1 predicted significantly more severe depressive symptoms at BD2, but only for adolescents with moderate (50th percentile) and high (84th percentile) levels of IL-6 and CRP at BD2. In conclusion, adolescents who experienced both recent stressful life events and larger increases in inflammatory activity following these stressors were at increased risk for more severe depressive symptoms after approximately one year. The findings indicate that the interaction of stress and larger changes in inflammatory activity following these stressors are prognostic risk factors for depression severity in adolescents.

Indexed as

Life Change EventsStress, PsychologicalUrban PopulationAdolescentBiomarkersChildC-Reactive ProteinDepressionFemaleHumansInflammationInterleukin-6MaleProspective StudiesRisk FactorsBiomarkersC-Reactive ProteinInterleukin-6AdolescenceAdversityDepressionInflammationStressful life events

Identifiers

PMID30822466
PMCPMC6710165
OpenAlexW2915906110

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.