Evidence map›Paper›PMID 35921104›Full record

ArticleJAMA psychiatry2022

Exploring Links Between Psychosis and Frontotemporal Dementia Using Multimodal Machine Learning: Dementia Praecox Revisited.

Nikolaos Koutsouleris, Christos Pantelis, Dennis Velakoulis, Philip McGuire, Dominic B Dwyer, Maria-Fernanda Urquijo-Castro, Riya Paul, Sen Dong, David Popovic, Oemer Oeztuerk and 32 more

Open access · hybridAbstract read
In one paragraph

Article in JAMA psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.8field-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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. A frontotemporal dementia-like phenotype in schizophrenia: links to striatal dopamine and iron accumulation.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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

42 authors at 20 institutions in 6 countries.

Nikolaos KoutsoulerisDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Christos PantelisMelbourne Neuropsychiatry Centre, University of Melbourne, Melbourne, Australia.
Dennis VelakoulisMelbourne Neuropsychiatry Centre, University of Melbourne, Melbourne, Australia.
Philip McGuireInstitute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
Dominic B DwyerDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Maria-Fernanda Urquijo-CastroDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Riya PaulDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Sen DongDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
David PopovicDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Oemer OeztuerkDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Joseph KambeitzDepartment of Psychiatry and Psychotherapy, University of Cologne, Cologne, Germany.
Raimo K R SalokangasDepartment of Psychiatry, University of Turku, Turku, Finland.
Jarmo HietalaDepartment of Psychiatry, University of Turku, Turku, Finland.
Alessandro BertolinoDepartment of Basic Medical Science, Neuroscience and Sense Organs, University of Bari Aldo Moro, Bari, Italy.
Paolo BrambillaDepartment of Neurosciences and Mental Health, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Rachel UpthegroveInstitute of Mental Health, University of Birmingham, Birmingham, United Kingdom.
Stephen J WoodSchool of Psychology, University of Birmingham, Birmingham, United Kingdom.
Rebekka LencerDepartment of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany.
Stefan BorgwardtDepartment of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany.
Carlo MajInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, University of Bonn, Bonn, Germany.
Markus NöthenInstitute of Human Genetics, School of Medicine, University Hospital Bonn, University of Bonn, Bonn, Germany.
Franziska DegenhardtInstitute of Human Genetics, School of Medicine, University Hospital Bonn, University of Bonn, Bonn, Germany.
Maryna PolyakovaDepartment of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Karsten MuellerDepartment of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Arno VillringerDepartment of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Adrian DanekDepartment of Neurology, Ludwig Maximilian University Munich, Munich, Germany.
Klaus FassbenderDepartment of Neurology, Saarland University Hospital, Homburg, Germany.
Klaus FliessbachDepartment of Psychiatry and Psychotherapy, University Hospital Bonn, Bonn, Germany.
Holger JahnDepartment of Psychiatry and Psychotherapy, University Hospital Hamburg, Hamburg, Germany.
Johannes KornhuberDepartment of Psychiatry and Psychotherapy, Friedrich Alexander University Erlangen-Nuremberg, Erlangen, Germany.
Bernhard LandwehrmeyerDepartment of Neurology, University of Ulm, Ulm, Germany.
Sarah Anderl-StraubDepartment of Neurology, University of Ulm, Ulm, Germany.
Johannes PrudloDepartment of Neurology, University Medicine Rostock, Rostock, Germany.
Matthis SynofzikGerman Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Jens WiltfangGerman Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Lina RiedlDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Munich, Germany.
Janine Diehl-SchmidDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Munich, Germany.
Markus OttoDepartment of Neurology, University of Ulm, Ulm, Germany.
Eva MeisenzahlDepartment of Psychiatry and Psychotherapy, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.
Peter FalkaiDepartment of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany.
Matthias L SchroeterDepartment of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
International FTD-Genetics Consortium (IFGC), the German Frontotemporal Lobar Degeneration (FTLD) Consortium, and the PRONIA Consortium
Ludwig-Maximilians-Universität München · DEThe University of Melbourne · AUUniversität Ulm · DEUniversity of Bonn · DEGerman Center for Neurodegenerative Diseases · DEKing's College London · GBMax Planck Institute for Human Cognitive and Brain Sciences · DETechnical University of Munich · DEUniversity Hospital Leipzig · DEUniversity of Turku · FIFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeinrich Heine University Düsseldorf · DEInstitute of Mental Health · GBSaarland University · DEUniversität Hamburg · DEUniversity Hospital Bonn · DEUniversity of Bari Aldo Moro · ITUniversity of Basel · CHUniversity of Cologne · DEUniversity of Lübeck · DE

Funding

Medical Research Council G0301152Medical Research Council MC_U105597119Medical Research Council MC_UU_00005/12Parkinson's UK G-1703
6 · The paper itself

Abstract

Importance: The behavioral and cognitive symptoms of severe psychotic disorders overlap with those seen in dementia. However, shared brain alterations remain disputed, and their relevance for patients in at-risk disease stages has not been explored so far. Objective: To use machine learning to compare the expression of structural magnetic resonance imaging (MRI) patterns of behavioral-variant frontotemporal dementia (bvFTD), Alzheimer disease (AD), and schizophrenia; estimate predictability in patients with bvFTD and schizophrenia based on sociodemographic, clinical, and biological data; and examine prognostic value, genetic underpinnings, and progression in patients with clinical high-risk (CHR) states for psychosis or recent-onset depression (ROD). Design, Setting, and Participants: This study included 1870 individuals from 5 cohorts, including (1) patients with bvFTD (n = 108), established AD (n = 44), mild cognitive impairment or early-stage AD (n = 96), schizophrenia (n = 157), or major depression (n = 102) to derive and compare diagnostic patterns and (2) patients with CHR (n = 160) or ROD (n = 161) to test patterns' prognostic relevance and progression. Healthy individuals (n = 1042) were used for age-related and cohort-related data calibration. Data were collected from January 1996 to July 2019 and analyzed between April 2020 and April 2022. Main Outcomes and Measures: Case assignments based on diagnostic patterns; sociodemographic, clinical, and biological data; 2-year functional outcomes and genetic separability of patients with CHR and ROD with high vs low pattern expression; and pattern progression from baseline to follow-up MRI scans in patients with nonrecovery vs preserved recovery. Results: Of 1870 included patients, 902 (48.2%) were female, and the mean (SD) age was 38.0 (19.3) years. The bvFTD pattern comprising prefrontal, insular, and limbic volume reductions was more expressed in patients with schizophrenia (65 of 157 [41.2%]) and major depression (22 of 102 [21.6%]) than the temporo-limbic AD patterns (28 of 157 [17.8%] and 3 of 102 [2.9%], respectively). bvFTD expression was predicted by high body mass index, psychomotor slowing, affective disinhibition, and paranoid ideation (R2 = 0.11). The schizophrenia pattern was expressed in 92 of 108 patients (85.5%) with bvFTD and was linked to the C9orf72 variant, oligoclonal banding in the cerebrospinal fluid, cognitive impairment, and younger age (R2 = 0.29). bvFTD and schizophrenia pattern expressions forecasted 2-year psychosocial impairments in patients with CHR and were predicted by polygenic risk scores for frontotemporal dementia, AD, and schizophrenia. Findings were not associated with AD or accelerated brain aging. Finally, 1-year bvFTD/schizophrenia pattern progression distinguished patients with nonrecovery from those with preserved recovery. Conclusions and Relevance: Neurobiological links may exist between bvFTD and psychosis focusing on prefrontal and salience system alterations. Further transdiagnostic investigations are needed to identify shared pathophysiological processes underlying the neuroanatomical interface between the 2 disease spectra.

Indexed as

Alzheimer DiseaseFrontotemporal DementiaPsychotic DisordersSchizophreniaAdultBrainFemaleHumansMachine LearningMagnetic Resonance ImagingMaleNeuropsychological Tests

Identifiers

PMID35921104
PMCPMC9350851
OpenAlexW4289593467

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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.