Evidence map›Paper›PMID 31168068›Full record

ArticleMolecular psychiatry2021

Increased levels of midbrain immune-related transcripts in schizophrenia and in murine offspring after maternal immune activation.

Tertia D Purves-Tyson, Ulrike Weber-Stadlbauer, Juliet Richetto, Debora A Rothmond, Marie A Labouesse, Marcello Polesel, Kate Robinson, Cynthia Shannon Weickert, Urs Meyer

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 3 pooled it
4.8field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 3 syntheses or guidelines pooled it, 129 citations in OpenAlex.

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  8. Mesocorticostriatal Reinforcement Learning of State Representation and Value with Implications for the Mechanisms of Schizophrenia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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10 more citing papers are in PubMed but not listed here.

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

9 authors at 5 institutions in 3 countries.

Tertia D Purves-TysonSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, NSW, 2031, Australia.ORCID http://orcid.org/0000-0003-2401-4266
Ulrike Weber-StadlbauerInstitute of Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich, Switzerland.
Juliet RichettoInstitute of Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich, Switzerland.
Debora A RothmondSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, NSW, 2031, Australia.
Marie A LabouessePhysiology and Behavior Laboratory, ETH Zurich, Schwerzenbach, Switzerland.
Marcello PoleselInstitute of Anatomy, University of Zurich, Zurich, Switzerland.
Kate RobinsonSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, NSW, 2031, Australia.ORCID http://orcid.org/0000-0002-4654-8456
Cynthia Shannon WeickertSchizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, NSW, 2031, Australia. cyndi@neura.edu.au.
Urs MeyerInstitute of Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich, Switzerland. urs.meyer@vetpharm.uzh.ch.ORCID http://orcid.org/0000-0001-7244-0345
University of Zurich · CHNeuroscience Research Australia · AUETH Zurich · CHSUNY Upstate Medical University · USUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathophysiology of dopamine dysregulation in schizophrenia involves alterations at the ventral midbrain level. Given that inflammatory mediators such as cytokines influence the functional properties of midbrain dopamine neurons, midbrain inflammation may play a role in schizophrenia by contributing to presynaptic dopamine abnormalities. Thus, we quantified inflammatory markers in dopaminergic areas of the midbrain of people with schizophrenia and matched controls. We also measured these markers in midbrain of mice exposed to maternal immune activation (MIA) during pregnancy, an established risk factor for schizophrenia and other psychiatric disorders. We found diagnostic increases in SERPINA3, TNFα, IL1β, IL6, and IL6ST transcripts in schizophrenia compared with controls (p < 0.02-0.001). The diagnostic differences in these immune markers were accounted for by a subgroup of schizophrenia cases (~ 45%, 13/28) showing high immune status. Consistent with the human cohort, we identified increased expression of immune markers in the midbrain of adult MIA offspring (SERPINA3, TNFα, and IL1β mRNAs, all p ≤ 0.01), which was driven by a subset of MIA offspring (~ 40%, 13/32) with high immune status. There were no diagnostic (human cohort) or group-wise (mouse cohort) differences in cellular markers indexing the density and/or morphology of microglia or astrocytes, but an increase in the transcription of microglial and astrocytic markers in schizophrenia cases and MIA offspring with high inflammation. These data demonstrate that immune-related changes in schizophrenia extend to dopaminergic areas of the midbrain and exist in the absence of changes in microglial cell number, but with putative evidence of microglial and astrocytic activation in the high immune subgroup. MIA may be one of the contributing factors underlying persistent neuroimmune changes in the midbrain of people with schizophrenia.

Indexed as

Prenatal Exposure Delayed EffectsSchizophreniaAnimalsBehavior, AnimalDisease Models, AnimalFemaleMesencephalonMiceMicrogliaPregnancy

Identifiers

PMID31168068
PMCPMC7910216
OpenAlexW2949039677

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.