Evidence map›Paper›PMID 26503033›Full record

ArticleHuman brain mapping2016

Impaired prefrontal synaptic gain in people with psychosis and their relatives during the mismatch negativity.

Siri Ranlund, Rick A Adams, Álvaro Díez, Miguel Constante, Anirban Dutt, Mei-Hua Hall, Amparo Maestro Carbayo, Colm McDonald, Sabrina Petrella, Katja Schulze and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Human brain mapping, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 81 citations in OpenAlex.

  1. Mismatch negativity matures in adolescence and without sensitivity to microglial depletion.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  2. Changes in Intrinsic Activity of the Primary Somatosensory Cortex Causally Explain Differences in Emotion Perception in Autism.Autism research : official journal of the International Society for Autism Research · 2026
    Article
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  15. Somatosensory Evoked Potentials Reveal Reduced Embodiment of Emotions in Autism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  16. Review
  17. GABANeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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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

15 authors at 10 institutions in 5 countries.

Siri RanlundDivision of Psychiatry, University College London, London, United Kingdom.
Rick A AdamsDivision of Psychiatry, University College London, London, United Kingdom.
Álvaro DíezDivision of Psychiatry, University College London, London, United Kingdom.
Miguel ConstanteDepartment of Psychiatry, Hospital Beatriz Angelo, Lisbon, Portugal.
Anirban DuttThe South London and Maudsley NHS Foundation Trust, NIHR Biomedical Research Centre for Mental Health at the Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Mei-Hua HallPsychology Research Laboratory, Harvard Medical School, McLean Hospital, Belmont, Massachusetts, USA.
Amparo Maestro CarbayoThe South London and Maudsley NHS Foundation Trust, NIHR Biomedical Research Centre for Mental Health at the Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Colm McDonaldDepartment of Psychiatry, Clinical Science Institute, National University of Ireland, Galway, Ireland.
Sabrina PetrellaThe South London and Maudsley NHS Foundation Trust, NIHR Biomedical Research Centre for Mental Health at the Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Katja SchulzeThe South London and Maudsley NHS Foundation Trust, University Hospital Lewisham, London, United Kingdom.
Madiha ShaikhThe South London and Maudsley NHS Foundation Trust, NIHR Biomedical Research Centre for Mental Health at the Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Muriel WalsheDivision of Psychiatry, University College London, London, United Kingdom.
Karl FristonThe Wellcome Trust Centre for Neuroimaging, Institute of Neurology, University College London, London, United Kingdom.
Dimitris PinotsisThe Wellcome Trust Centre for Neuroimaging, Institute of Neurology, University College London, London, United Kingdom.
Elvira BramonDivision of Psychiatry, University College London, London, United Kingdom.
University College London · GBKing's College London · GBCentre for Mental Health · GBHarvard University · USHospital Beatriz Ângelo · PTImperial College London · GBNational University of Ireland · IEThe London College · GBUniversity Hospital Lewisham · GBWellcome Centre for Human Neuroimaging · GB

Funding

Neurobiological Markers as Predictors of Later Functional Outcome in First Episode PsychosisR01MH109687 · NIMH · MCLEAN HOSPITAL · PI HALL, MEI-HUA · 2016 to 2021
$2.5M
Department of Health PDA/02/06/016Medical Research Council G0901310NIMH NIH HHS R01 MH109687Wellcome Trust 085475/B/08/ZWellcome Trust 085475/Z/08/ZWellcome Trust 088130Wellcome Trust 088130/Z/09/ZWellcome Trust 091593
6 · The paper itself

Abstract

The mismatch negativity (MMN) evoked potential, a preattentive brain response to a discriminable change in auditory stimulation, is significantly reduced in psychosis. Glutamatergic theories of psychosis propose that hypofunction of NMDA receptors (on pyramidal cells and inhibitory interneurons) causes a loss of synaptic gain control. We measured changes in neuronal effective connectivity underlying the MMN using dynamic causal modeling (DCM), where the gain (excitability) of superficial pyramidal cells is explicitly parameterised. EEG data were obtained during a MMN task--for 24 patients with psychosis, 25 of their first-degree unaffected relatives, and 35 controls--and DCM was used to estimate the excitability (modeled as self-inhibition) of (source-specific) superficial pyramidal populations. The MMN sources, based on previous research, included primary and secondary auditory cortices, and the right inferior frontal gyrus. Both patients with psychosis and unaffected relatives (to a lesser degree) showed increased excitability in right inferior frontal gyrus across task conditions, compared to controls. Furthermore, in the same region, both patients and their relatives showed a reversal of the normal response to deviant stimuli; that is, a decrease in excitability in comparison to standard conditions. Our results suggest that psychosis and genetic risk for the illness are associated with both context-dependent (condition-specific) and context-independent abnormalities of the excitability of superficial pyramidal cell populations in the MMN paradigm. These abnormalities could relate to NMDA receptor hypofunction on both pyramidal cells and inhibitory interneurons, and appear to be linked to the genetic aetiology of the illness, thereby constituting potential endophenotypes for psychosis.

Indexed as

FamilyAcoustic StimulationAdolescentAdultBrain InjuriesContingent Negative VariationElectroencephalographyEvoked Potentials, AuditoryFemaleHumansMaleMiddle AgedModels, TheoreticalNonlinear DynamicsPrefrontal CortexPsychotic Disorderscortical excitabilitycortical gainDCMdynamic causal modelingeffective connectivitygenetic riskNMDA receptorpsychosisschizophreniaunaffected relatives

Identifiers

PMID26503033
PMCPMC4843949
OpenAlexW2346160145

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.