Evidence map›Paper›PMID 26346639›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Social Stress and Psychosis Risk: Common Neurochemical Substrates?

Romina Mizrahi

Open access · bronzeAbstract readReview
In one paragraph

Review in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Adolescents' internalizing and externalizing symptom trajectories in relation to early-life parental depressive symptoms.European psychiatry : the journal of the Association of European Psychiatrists · 2025
    Article
  8. Article
  9. Stress and the City: Mental Health in Urbanized vs. Rural Areas in Salzburg, Austria.International journal of environmental research and public health · 2024
    Article
  10. Article
  11. Review
  12. Stress, Environment and Early Psychosis.Current neuropharmacology · 2024
    Review
  13. Article
  14. Review
  15. Review
  16. COVID-19 and New-Onset Psychosis: A Comprehensive Review.Journal of personalized medicine · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

1 author at 1 institution in 1 country.

Romina MizrahiResearch Imaging Centre, PET Centre, Centre for Addiction and Mental Health (CAMH)-Clarke Division and University of Toronto, Toronto, ON, Canada.
Centre for Addiction and Mental Health · CA

Funding

Imaging Neuroinflammation in Clinical high risk and SchizophreniaR01MH100043 · NIMH · CENTRE FOR ADDICTION AND MENTAL HEALTH · PI MIZRAHI, ROMINA · 2014 to 2018
$1.6M
Canadian Institutes of Health ResearchNIMH NIH HHS R01 MH100043NIMH NIH HHS R01MH100043
6 · The paper itself

Abstract

Environmental risk factors have been implicated in the etiology of psychotic disorders, with growing evidence showing the adverse effects of migration, social marginalization, urbanicity, childhood trauma, social defeat, and other adverse experiences on mental health in vulnerable populations. Collectively, social stress may be one mechanism that could link these environmental risk factors. The exact mechanism(s) by which social stress can affect brain function, and in particular the molecular targets involved in psychosis (such as the dopaminergic (DA) system), is (are) not fully understood. In this review, we will discuss the interplay between social environmental risk factors and molecular changes in the human brain; in particular, we will highlight the impact of social stress on three specific neurochemical systems: DA, neuroinflammation/immune, and endocannabinoid (eCB) signaling. We have chosen the latter two molecular pathways based on emerging evidence linking schizophrenia to altered neuroinflammatory processes and cannabis use. We further identify key developmental periods in which social stress interacts with these pathways, suggesting window(s) of opportunities for novel interventions. Taken together, we suggest that they may have a key role in the pathogenesis and disease progression, possibly provide novel treatment options for schizophrenia, and perhaps even prevent it.

Indexed as

Social PerceptionAnimalsBrainDopamineHumansPsychotic DisordersStress, PsychologicalDopamine

Identifiers

PMID26346639
PMCPMC4707841
OpenAlexW1886307983

What OpenQuestion holds

Textmetadata
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.