Evidence map›Paper›PMID 39562461›Full record

ReviewAdvances in neurobiology2024

Categorical and Dimensional Approaches for Psychiatric Classification and Treatment Targeting: Considerations from Psychosis Biotypes.

Brett A Clementz, Michal Assaf, John A Sweeney, Elliot S Gershon, Sarah K Keedy, S Kristian Hill, Elena I Ivleva, Carol A Tamminga, Jennifer E McDowell, Matcheri S Keshavan and 3 more

Abstract readReview
In one paragraph

Review in Advances in neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

13 authors.

Brett A ClementzDepartments of Psychology and Neuroscience, BioImaging Research Center, University of Georgia, Athens, GA, USA. clementz@uga.edu.
Michal AssafDepartment of Psychiatry, Olin Neuropsychiatric Research Center, Hartford, CT, USA.
John A SweeneyDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH, USA.
Elliot S GershonDepartments of Psychiatry and Human Genetics, University of Chicago, Chicago, IL, USA.
Sarah K KeedyDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA.
S Kristian HillDepartment of Psychology, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Elena I IvlevaDepartment of Psychiatry, UT Southwestern Medical School, Dallas, TX, USA.
Carol A TammingaDepartment of Psychiatry, UT Southwestern Medical School, Dallas, TX, USA.
Jennifer E McDowellDepartments of Psychology and Neuroscience, Owen Institute for Behavioral Research, University of Georgia, Athens, GA, USA.
Matcheri S KeshavanDepartment of Psychiatry, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Robert D GibbonsDepartments of Medicine and Public Health Sciences, University of Chicago, Chicago, IL, USA.
William T CarpenterDepartment of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD, USA.
Godfrey D PearlsonDepartments of Psychiatry and Neuroscience, Olin Neuropsychiatric Research Center, Institute of Living, Hartford Hospital, and Yale University School of Medicine, Hartford, CT, USA.

Funding

Research Support CoreP50DA051361 · NIDA · UNIVERSITY OF GEORGIA · PI EHRLICH, KATHERINE BABCOCK · 2020 to 2024
$9.7M
5/5 BIPOLAR-SCHIZOPHRENIA NETWORK FOR INTERMEDIATE PHENOTYPES (B-SNIP) - Resubmission - 1R01MH103366 · NIMH · UNIVERSITY OF GEORGIA · PI CLEMENTZ, BRETT A, GIBBONS, ROBERT D · 2015 to 2019
$3.8M
Neural Architecture of Social Emotional Processing and Regulation in Autism Spectrum Disorder: A Dynamic Connectivity PerspectiveR01MH119069 · NIMH · HARTFORD HOSPITAL · PI ASSAF, MICHAL · 2019 to 2023
$3.6M
The Social Brain in Schizophrenia and Autism Spectrum DisordersR01MH095888 · NIMH · HARTFORD HOSPITAL · PI ASSAF, MICHAL · 2012 to 2016
$2.6M
2/5-Clozapine Response and Biomarker Correlates in Low-IEA Biotype-1R01MH124804 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S, KEEDY, SARAH K · 2021 to 2025
$1.8M
5/5: Selective Antipsychotic Response to Clozapine in B-SNIP Biotype-1 (CLOZAPINE)R01MH124803 · NIMH · UNIVERSITY OF GEORGIA · PI CLEMENTZ, BRETT A · 2021 to 2025
$1.6M
5/5 - Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services (BICEPS)R01MH127172 · NIMH · UNIVERSITY OF GEORGIA · PI BRETT A CLEMENTZ · 2022 to 2026
$1.4M
Identification of distributed neural sources of the auditory steady-state response in psychosis BiotypesR21MH126398 · NIMH · UNIVERSITY OF GEORGIA · PI CLEMENTZ, BRETT A · 2022 to 2023
$415k
1/2: B-SNIP: Algorithmic Diagnostics for Efficient Prescription of Treatments (ADEPT)R01MH124806 · NIMH · UNIVERSITY OF GEORGIA · PI CLEMENTZ, BRETT A · 2021 to 2021
$302k
NIDA NIH HHS P50 DA051361NIMH NIH HHS R01 MH095888NIMH NIH HHS R01 MH103366NIMH NIH HHS R01 MH119069NIMH NIH HHS R01 MH124803NIMH NIH HHS R01 MH124804NIMH NIH HHS R01 MH124806NIMH NIH HHS R01 MH127172NIMH NIH HHS R21 MH126398
6 · The paper itself

Abstract

Categorical diagnosis, a pillar of the medical model, has not worked well in psychiatry where most diagnoses are still exclusively symptom based. Uncertainty continues about whether categories or dimensions work better for the assessment and treatment of idiopathic psychoses. The Bipolar Schizophrenia Network for Intermediate Phenotypes (B-SNIP) examined multiple cognitive and electrophysiological biomarkers across a large transdiagnostic psychosis data set. None of the variables supported neurobiological distinctiveness for conventional clinical psychosis diagnoses but showed a continuum of severity. Using numerical taxonomy of these data, B-SNIP identified three biological subtypes (Biotypes) agnostic to DSM diagnoses. Biotype-1 is characterized by reduced physiological response to salient stimuli, while Biotype-2 showed accentuated intrinsic (background or ongoing) neural activity and the worst inhibition. Biotype-3 cases are like healthy persons on many laboratory measures. These Biotypes differed in imaging and other electrophysiological measures not included in subgroup creation, illustrating external validation. The Biotypes solution also replicated in an independent sample of psychosis cases. Biotypes are differentiable by clinical characteristics, leading to a feasible algorithm for Biotype estimates. Identifying Biotypes may aid treatment selection and outcome prediction. As an example, preliminary cross-sectional B-SNIP data suggest that Biotype-1 cases may have physiological features that predict a more favorable response to clozapine. While psychosis Biotypes reveal physiological heterogeneity across cases with similar clinical characteristics, data also suggest a dimensional vulnerability for serious psychopathology that cuts across diagnostic boundaries. Both categorical and dimensional diagnostic approaches should be considered within idiopathic psychosis for optimum diagnosis, care, and research.

Indexed as

Psychotic DisordersAntipsychotic AgentsBiomarkersHumansSchizophreniaAntipsychotic AgentsBiomarkersBiotypesCategoricalClassificationCognitionDimensionalPhysiologyPsychosis

Identifiers

PMID39562461
PMCPMC12054367

What OpenQuestion holds

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Registered trials

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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.