Evidence map›Paper›PMID 30836740›Full record

ArticlePsychiatry investigation2019

Peripheral Biomarkers for First-Episode Psychosis-Opportunities from the Neuroinflammatory Hypothesis of Schizophrenia.

Nuno Trovão, Joana Prata, Orlando VonDoellinger, Susana Santos, Mário Barbosa, Rui Coelho

Open access · diamondAbstract read
In one paragraph

Article in Psychiatry investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 5 pooled it
1.8field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 5 syntheses or guidelines pooled it, 54 citations in OpenAlex.

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  11. Changes in schizophrenia symptoms, tryptophan metabolism, neuroinflammation and the GABA-glutamate loop: A pilot study.The South African journal of psychiatry : SAJP : the journal of the Society of Psychiatrists of South Africa · 2025
    Article
  12. White matter lipidome alterations in the schizophrenia brain.Schizophrenia (Heidelberg, Germany) · 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 3 institutions in 1 country.

Nuno TrovãoDepartment of Psychiatry, Vila Nova de Gaia/ Espinho Hospital Center, Vila Nova de Gaia, Portugal.
Joana PrataDepartment of Psychiatry, Vila Nova de Gaia/ Espinho Hospital Center, Vila Nova de Gaia, Portugal.
Orlando VonDoellingerInstituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
Susana SantosInstituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
Mário BarbosaInstituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
Rui CoelhoInstituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
Universidade do Porto · PTCentro Hospitalar de Vila Nova de Gaia · PTi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PT

Funding

Portuguese Foundation for Science and Technology
6 · The paper itself

Abstract

objectiveSchizophrenia is a disabling disorder of unknown aetiology, lacking definite diagnostic method and cure. A reliable biological marker of schizophrenia is highly demanded, for which traceable immune mediators in blood could be promising candidates. We aimed to gather the best findings of neuroinflammatory markers for first-episode psychosis (FEP).

methodsWe performed an extensive narrative review of online literature on inflammation-related markers found in human FEP patients only.

resultsChanges to cytokine levels have been increasingly reported in schizophrenia. The peripheral levels of IL-1 (or its receptor antagonist), soluble IL-2 receptor, IL-4, IL-6, IL-8, and TNF-α have been frequently reported as increased in FEP, in a suggestive continuum from high-risk stages for psychosis. Microglia and astrocytes establish the link between this immune signalling and the synthesis of noxious tryptophan catabolism products, that cause structural damage and directly hamper normal neurotransmission. Amongst these, only 3-hydroxykynurenine has been consistently described in the blood of FEP patients.

conclusionPeripheral molecules stemming from brain inflammation might provide insightful biomarkers of schizophrenia, as early as FEP or even prodromal phases, although more time- and clinically-adjusted studies are essential for their validation.

Indexed as

BiomarkersFirst-episode psychosisImmuneNeuroinflammationSchizophrenia

Identifiers

PMID30836740
PMCPMC6444098
OpenAlexW2921240859

What OpenQuestion holds

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LicenceCC BY-NC
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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.