Evidence map›Paper›PMID 38824135›Full record

ArticleTranslational psychiatry2024

Inflammation and immune system pathways as biological signatures of adolescent depression-the IDEA-RiSCo study.

Valentina Zonca, Moira Marizzoni, Samantha Saleri, Zuzanna Zajkowska, Pedro H Manfro, Laila Souza, Anna Viduani, Luca Sforzini, Johnna R Swartz, Helen L Fisher and 5 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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

15 authors.

Valentina ZoncaKing's College London, Department of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, London, UK. valentina.zonca@unimi.it.ORCID 0000-0002-6628-5999
Moira MarizzoniBiological Psychiatry Unit, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Via Pilastroni, 4, 25125, Brescia, Italy.
Samantha SaleriBiological Psychiatry Unit, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Via Pilastroni, 4, 25125, Brescia, Italy.
Zuzanna ZajkowskaKing's College London, Department of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, London, UK.ORCID 0000-0002-5214-305X
Pedro H ManfroDepartment of Psychiatry, Universidade Federal do Rio Grande do Sul, Child & Adolescent Psychiatry Division, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos, 2350-400N, Porto Alegre, RS, 90035-903, Brazil.
Laila SouzaDepartment of Psychiatry, Universidade Federal do Rio Grande do Sul, Child & Adolescent Psychiatry Division, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos, 2350-400N, Porto Alegre, RS, 90035-903, Brazil.
Anna ViduaniDepartment of Psychiatry, Universidade Federal do Rio Grande do Sul, Child & Adolescent Psychiatry Division, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos, 2350-400N, Porto Alegre, RS, 90035-903, Brazil.ORCID 0000-0002-6289-6397
Luca SforziniKing's College London, Department of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, London, UK.ORCID 0000-0001-6795-0391
Johnna R SwartzDepartment of Human Ecology, University of California, Davis, Davis, CA, 95616, USA.
Helen L FisherKing's College London, Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, London, UK.ORCID 0000-0003-4174-2126
Brandon A KohrtCenter for Global Mental Health Equity, Department of Psychiatry and Behavioral Health, School of Medicine and Health Sciences, The George Washington University, 2120 L St NW, Ste 600, Washington, DC, 20037D, USA.
Christian KielingDepartment of Psychiatry, Universidade Federal do Rio Grande do Sul, Child & Adolescent Psychiatry Division, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos, 2350-400N, Porto Alegre, RS, 90035-903, Brazil.
Marco Andrea RivaDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-1699-5060
Annamaria CattaneoDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.
Valeria MondelliKing's College London, Department of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, London, UK.ORCID 0000-0001-8690-6839

Funding

Brazilian-American Initiative on Neuroimaging for Identifying Depression Early in Adolescence (BRAIN-IDEA)R21MH124072 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KIELING, CHRISTIAN, SWARTZ, JOHNNA ROSE · 2020 to 2020
$346k
Medical Research Council MC_PC_MR/R019460/1NIMH NIH HHS R21 MH124072RCUK | Economic and Social Research Council (ESRC) ES/S012567/1
6 · The paper itself

Abstract

The biological mechanisms underlying the onset of major depressive disorder (MDD) have predominantly been studied in adult populations from high-income countries, despite the onset of depression typically occurring in adolescence and the majority of the world's adolescents living in low- and middle-income countries (LMIC). Taking advantage of a unique adolescent sample in an LMIC (Brazil), this study aimed to identify biological pathways characterizing the presence and increased risk of depression in adolescence, and sex-specific differences in such biological signatures. We collected blood samples from a risk-stratified cohort of 150 Brazilian adolescents (aged 14-16 years old) comprising 50 adolescents with MDD, 50 adolescents at high risk of developing MDD but without current MDD, and 50 adolescents at low risk of developing MDD and without MDD (25 females and 25 males in each group). We conducted RNA-Seq and pathway analysis on whole blood. Inflammatory-related biological pathways, such as role of hypercytokinemia/hyperchemokinemia in the pathogenesis of influenza (z-score = 3.464, p < 0.001), interferon signaling (z-score = 2.464, p < 0.001), interferon alpha/beta signaling (z-score = 3.873, p < 0.001), and complement signaling (z-score = 2, p = 0.002) were upregulated in adolescents with MDD compared with adolescents without MDD independently from their level of risk. The up-regulation of such inflammation-related pathways was observed in females but not in males. Inflammatory-related pathways involved in the production of cytokines and in interferon and complement signaling were identified as key indicators of adolescent depression, and this effect was present only in females.

Indexed as

InflammationMajor Depressive DisorderAdolescentBrazilCytokinesFemaleHumansImmune SystemMaleSex FactorsCytokines

Identifiers

PMID38824135
PMCPMC11144232

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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.