Evidence map›Paper›PMID 23890736›Full record

ReviewBiological psychiatry2014

Immune system disturbances in schizophrenia.

Szatmár Horváth, Károly Mirnics

Abstract readReview
In one paragraph

Review in Biological psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
4.7field-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

99 citing papers in PubMed, 183 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

39 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

2 authors at 1 institution in 2 countries.

Szatmár HorváthDepartment of Psychiatry, Vanderbilt University, Nashville, Tennessee; Department of Psychiatry, University of Szeged, 6725 Szeged, Hungary.
Károly MirnicsDepartment of Psychiatry, Vanderbilt University, Nashville, Tennessee; Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, Tennessee; Department of Psychiatry, University of Szeged, 6725 Szeged, Hungary. Electronic address: karoly.mirnics@vanderbilt.edu.
University of Szeged · HU

Funding

THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Neocortical Transcriptome Changes in SchizophreniaR01MH067234 · NIMH · VANDERBILT UNIVERSITY · PI MIRNICS, KAROLY · 2003 to 2021
$4.7M
Neuroimmune Changes in SchizophreniaR01MH079299 · NIMH · VANDERBILT UNIVERSITY · PI MIRNICS, KAROLY · 2007 to 2011
$1.7M
Uncovering complex expression patterns in schizophreniaK02MH070786 · NIMH · VANDERBILT UNIVERSITY · PI MIRNICS, KAROLY · 2004 to 2008
$527k
NICHD NIH HHS P30 HD015052NIMH NIH HHS K02 MH070786NIMH NIH HHS R01 MH067234NIMH NIH HHS R01MH067234NIMH NIH HHS R01 MH079299
6 · The paper itself

Abstract

Epidemiological, genetic, transcriptome, postmortem, peripheral biomarker, and therapeutic studies of schizophrenia all point to a dysregulation of both innate and adaptive immune systems in the disease, and it is likely that these immune changes actively contribute to disease symptoms. Gene expression disturbances in the brain of subjects with schizophrenia show complex, region-specific changes with consistently replicated and potentially interdependent induction of serpin peptidase inhibitor, clade A member 3 (SERPINA3) and interferon inducible transmembrane protein (IFITM) family transcripts in the prefrontal cortex. Recent data suggest that IFITM3 expression is a critical mediator of maternal immune activation. Because the IFITM gene family is primarily expressed in the endothelial cells and meninges, and because the meninges play a critical role in interneuron development, we suggest that these two non-neuronal cell populations might play an important role in the disease pathophysiology. Finally, we propose that IFITM3 in particular might be a novel, appealing, knowledge-based drug target for treatment of schizophrenia.

Indexed as

AnimalsAnti-Inflammatory AgentsBrainFemaleGenetic Predisposition to DiseaseHumansMaternal ExposureMembrane ProteinsPregnancyPregnancy Complications, InfectiousRNA-Binding ProteinsSchizophreniaSerpinsTranscriptomeAnti-Inflammatory AgentsIFITM3 protein, humanMembrane ProteinsRNA-Binding ProteinsSERPINA3 protein, humanSerpinsBlood-brain barrierblood vesselsCD14CHI3L1IFITMIFITM3immunemeningespia materpostmortemschizophreniaSERPINA3

Identifiers

PMID23890736
PMCPMC3841236
OpenAlexW2060928023

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.