Evidence map›Paper›PMID 41256675›Full record

ArticlebioRxiv : the preprint server for biology2025

Schizophrenia, variability, and the Anna Karenina principle.

Michael Murphy, Dost Öngür

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Michael MurphyMcLean Hospital; Belmont, MA, 02447, USA.
Dost ÖngürMcLean Hospital; Belmont, MA, 02447, USA.

Funding

Excitation-inhibition imbalance, posteromedial cortical dysconnectivity, and thought disorder in first-episode psychosisK23MH118565 · NIMH · MCLEAN HOSPITAL · PI MURPHY, MICHAEL J · 2019 to 2023
$983k
NIMH NIH HHS K23 MH118565
6 · The paper itself

Abstract

In neuroimaging studies of people with schizophrenia there is often higher within group variance in the patient group compared to the control group. This is counterintuitive - why would a subset of people selected because they all have the same disease be more varied than the general population? We used simulated data and real neuroimaging data to identify a potential cause of elevated variance in populations of patients with schizophrenia. We demonstrated that elevated variance can arise within variables that are unrelated to disease status simply because people with a set of neurological perturbations that cause schizophrenia are more likely to have higher numbers of perturbations overall. Additionally, we showed that observed elevated variances in people with schizophrenia can be reproduced by models that only rely on perturbation count. These results highlight an important barrier in our attempts to understand the pathophysiology of schizophrenia. Standard statistical practices in schizophrenia research do not account for the fact that schizophrenia is, at every level of analysis that has been studied, highly heterogeneous. This heterogeneity by itself is sufficient to produce elevated variances. Our work suggests that the most effective way to prevent schizophrenia may not be to identify and mitigate specific pathologies but rather to reduce the impact of broadly damaging factors such as those associated with poverty.

Identifiers

PMID41256675
PMCPMC12621827

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.