Evidence map›Paper›PMID 33536130›Full record

Trial reportBiological psychiatry2021

Relationship Between Serum NMDA Receptor Antibodies and Response to Antipsychotic Treatment in First-Episode Psychosis.

Thomas A Pollak, Angela Vincent, Conrad Iyegbe, Ester Coutinho, Leslie Jacobson, Dan Rujescu, James Stone, Julie Jezequel, Veronique Rogemond, Stephane Jamain and 8 more

Erratum issued 2 registry-linked trialsOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Biological psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 15% 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.

NCT01248195 phase4completednot on this map

Optimization of Treatment and Management of Schizophrenia in Europe

TypeinterventionalSponsorRene KahnRan2011 to 2016Enrolled479ConditionsSchizophrenia, Schizophreniform Disorder, Schizoaffective DisorderArmsAmisulpride open label, 6-week amisulpride double blind treatment, 6-week olanzapine double blind treatment, 12-week clozapine open-label treatment, Psychosocial intervention
NCT06321588 recruitingnot on this mapstarted 2023, after this paper: background citation

Autoimmune Dementia: Predictors of Neuronal Synaptic Antibodies in Patients With New-ONset Cognitive Impairment and Their Relevance in Non-encephalitic formS: The ADONIS Study

TypeobservationalSponsorAzienda Usl di BolognaRan2023 to 2026Enrolled300ConditionsCognitive Impairment, Dementia
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Autoimmune neuropsychiatric disorders manifesting with psychosis.The Journal of clinical investigation · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Autoantibody Encephalitis: Presentation, Diagnosis, and Management.Journal of clinical neurology (Seoul, Korea) · 2022
    Review
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 10 institutions in 4 countries.

Thomas A PollakDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom; South London and Maudsley NHS Foundation Trust, University College London, London, United Kingdom. Electronic address: thomas.pollak@kcl.ac.uk.
Angela VincentNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom.
Conrad IyegbeDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom.
Ester CoutinhoDivision of Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom.
Leslie JacobsonNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom.
Dan RujescuDepartment of Psychiatry, Psychotherapy, and Psychosomatics, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
James StoneDepartment of Neuroimaging, Centre for Neuroimaging Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom; South London and Maudsley NHS Foundation Trust, University College London, London, United Kingdom.
Julie JezequelCentre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
Veronique RogemondRare Disease Reference Center on Autoimmune Encephalitis, Hospices Civils de Lyon, Institut NeuroMyoGene Institut National de la Santé et de la Recherche Médicale U1217/Centre National de la Recherche Scientifique, University Claude Bernard, Universite de Lyon, Lyon, France.
Stephane JamainPsychiatry and Addictology Department (DMU IMPACT), University Paris Est Créteil, Hopitaux Universitaires Henri Mondor, L'Assistance Publique-Hôpitaux de Paris, Créteil, France.
Laurent GrocInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
Anthony DavidInstitute of Mental Health, University College London, London, United Kingdom.
Alice EgertonDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom.
Rene S KahnDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York.
Jerome HonnoratRare Disease Reference Center on Autoimmune Encephalitis, Hospices Civils de Lyon, Institut NeuroMyoGene Institut National de la Santé et de la Recherche Médicale U1217/Centre National de la Recherche Scientifique, University Claude Bernard, Universite de Lyon, Lyon, France.
Paola DazzanDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom.
Marion LeboyerPsychiatry and Addictology Department (DMU IMPACT), University Paris Est Créteil, Hopitaux Universitaires Henri Mondor, L'Assistance Publique-Hôpitaux de Paris, Créteil, France; Translational Neuropsychiatry Laboratory, Institut National de la Santé et de la Recherche Médicale U955, Créteil, France; FondaMental Foundation, Créteil, France.
Philip McGuireDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's Health Partners, King's College London, London, United Kingdom; South London and Maudsley NHS Foundation Trust, University College London, London, United Kingdom.
King's College London · GBJohn Radcliffe Hospital · GBUniversité Claude Bernard Lyon 1 · FRUniversité de Bordeaux · FRIcahn School of Medicine at Mount Sinai · USInserm · FRInstitute of Mental Health · GBMartin Luther University Halle-Wittenberg · DEUniversité Paris-Est Créteil · FRWellcome Centre for Human Neuroimaging · GB

Funding

Medical Research Council MC_PC_11003MRF_ C0439Wellcome TrustWellcome Trust 105758/Z/14/Z
6 · The paper itself

Abstract

backgroundWhen psychosis develops in NMDA receptor (NMDAR) antibody encephalitis, it usually has an acute or subacute onset, and antipsychotic treatment may be ineffective and associated with adverse effects. Serum NMDAR antibodies have been reported in a minority of patients with first-episode psychosis (FEP), but their role in psychosis onset and response to antipsychotic treatment is unclear.

methodsSera from 387 patients with FEP (duration of psychosis <2 years, minimally or never treated with antipsychotics) undergoing initial treatment with amisulpride as part of the OPTiMiSE (Optimization of Treatment and Management of Schizophrenia in Europe) trial (ClinicalTrials.gov number NCT01248195) were tested for NMDAR IgG antibodies using a live cell-based assay. Symptom severity was assessed using the Positive and Negative Syndrome Scale and the Clinical Global Impressions Scale at baseline and again after 4 weeks of treatment with amisulpride.

resultsAt baseline, 15 patients were seropositive for NMDAR antibodies and 372 were seronegative. The seropositive patients had similar symptom profiles and demographic features to seronegative patients but a shorter duration of psychosis (median 1.5 vs. 4.0 months; p = .031). Eleven seropositive and 284 seronegative patients completed 4 weeks of amisulpride treatment: after treatment, there was no between-groups difference in improvement in Positive and Negative Syndrome Scale scores or in the frequency of adverse medication effects.

conclusionsThese data suggest that in FEP, NMDAR antibody seropositivity alone is not an indication for using immunotherapy instead of antipsychotic medications. Further studies are required to establish what proportion of patients with FEP who are NMDAR antibody seropositive have coexisting cerebrospinal fluid inflammatory changes or other paraclinical evidence suggestive of a likely benefit from immunotherapy.

Indexed as

Antipsychotic AgentsPsychotic DisordersSchizophreniaEuropeHumansReceptors, N-Methyl-D-AspartateAntipsychotic AgentsReceptors, N-Methyl-D-AspartateAntipsychoticsAutoantibodiesBiomarkersFirst-episode psychosisImmunopsychiatryNMDA receptor

Identifiers

PMID33536130
PMCPMC8191702
OpenAlexW3108470754

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.