Evidence map›Paper›PMID 30851376›Full record

ArticleBrain, behavior, and immunity2019

Depressive symptoms and immune transcriptional profiles in late adolescents.

Jessica J Chiang, Steve W Cole, Julienne E Bower, Michael R Irwin, Shelley E Taylor, Jesusa Arevalo, Andrew J Fuligni

Open access · bronzeAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Chronic Treatment withInternational journal of molecular sciences · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Jessica J ChiangInstitute for Policy Research, Northwestern University, United States. Electronic address: jessica.chiang@northwestern.edu.
Steve W ColeDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, United States; Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, United States.
Julienne E BowerDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, United States; Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, United States; Department of Psychology, University of California, Los Angeles, United States.
Michael R IrwinDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, United States; Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, United States; Department of Psychology, University of California, Los Angeles, United States.
Shelley E TaylorDepartment of Psychology, University of California, Los Angeles, United States.
Jesusa ArevaloDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, United States; Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, United States.
Andrew J FuligniDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, United States; Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, United States; Department of Psychology, University of California, Los Angeles, United States.
University of California, Los Angeles · USNeurobehavioral Systems · USNorthwestern University · US

Funding

USC/UCLA Center on Biodemography &Population HealthP30AG017265 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE, HIRAM BELTRAN-SANCHEZ · 1999 to 2026
$17.9M
Statistics and Methods CoreR24HD041022 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COSTA, DORA L · 2001 to 2016
$10.1M
UCLA OLDER AMERICANS INDEPENDENCE CENTERP30AG028748 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MOORE, ALISON AHERN · 2006 to 2017
$9.8M
Scientific and Technical CoreP2CHD041022 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Martha Jane Bailey · 2016 to 2026
$6.9M
Daily Experience in Adolescence and Biomarkers of Early Risk for Adult HealthR01HD062547 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FULIGNI, ANDREW J · 2010 to 2015
$2.6M
Interdisciplinary Research Network on Early Adversity & Later Life ReversibilityU24AG047867 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GODFREY, KEITH, MCEWEN, BRUCE S. · 2014 to 2018
$954k
Adolescent Family Stress and Early Cardiovascular Risk: Psychosocial and Behavioral PathwaysF32HL134276 · NHLBI · NORTHWESTERN UNIVERSITY · PI CHIANG, JESSICA · 2016 to 2018
$166k
NHLBI NIH HHS F32 HL134276NIA NIH HHS P30 AG017265NIA NIH HHS P30 AG028748NIA NIH HHS U24 AG047867NICHD NIH HHS P2C HD041022NICHD NIH HHS R01 HD062547NICHD NIH HHS R24 HD041022
6 · The paper itself

Abstract

backgroundRates of depression increase and peak during late adolescence and alterations in immune processes are thought to be both a risk factor and outcome of depression. However, few studies have examined depression-immune dynamics among adolescents. Using a functional genomics approach, the current study examined whether depressive symptoms were associated with activation of a gene expression profile, characterized by upregulated expression of pro-inflammatory-related genes and downregulated expression of antiviral-related genes in a sample of older adolescents (M

methodParticipants (n = 87) reported on their depressive symptoms during the past week using the CES-D, and provided blood samples for genome-wide transcriptional profiling of mRNA.

resultsAdolescents with clinically-significant levels of depressive symptoms (CES-D ≥ 16) exhibited upregulated expression of inflammation-related genes and downregulated expression of antiviral-related genes compared to their peers with lower levels of depressive symptoms (CES-D < 16). Bioinformatics analyses suggested that this pattern of differential gene expression was mediated by greater activity of the pro-inflammatory transcription factor, nuclear factor-kappa B (NF-κB), and reduced activity of glucocorticoid receptors (GRs) and interferon response factors (IRFs). Additional analyses implicated monocytes, B cells, and dendritic cells as primary cellular sources of the observed gene expression patterns associated with depressive symptoms.

conclusionResults are consistent with past work demonstrating links between depression and altered immunity. They provide a molecular basis for these associations and suggest that the underlying molecular signature may emerge as early as late adolescence when rates of depression tend to increase.

Indexed as

AdolescentDepressionDepressive DisorderFemaleGene Expression ProfilingGene Expression RegulationGenomicsHumansInflammationMaleNF-kappa BReceptors, GlucocorticoidTranscriptomeYoung AdultNF-kappa BReceptors, Glucocorticoid

Identifiers

PMID30851376
PMCPMC6710012
OpenAlexW2922153932

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.