ArticlemedRxiv : the preprint server for health sciences2025
Latent class analysis of symptoms across schizophrenia, schizoaffective disorder, and bipolar I disorder.
Dana M Lapato, Roseann E Peterson, Eric D Achtyes, Peter F Buckley, Ayman H Fanous, Douglas S Lehrer, Humberto Nicolini, Dolores Malaspina, Mark H Rapaport, GPC Investigators and 4 more
Abstract readPreprint
In one paragraphArticle in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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0citing papers in PubMed
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1 · What the graph read from itWhat 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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
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4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
14 authors.
Dana M LapatoVirginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8169-9754 Roseann E PetersonInstitute for Genomics in Health, Department of Psychiatry and Behavioral Health, Downstate Health Sciences University; Dept. of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-6402-849X Eric D AchtyesWestern Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, USA.ORCID 0000-0001-8939-1535 Peter F BuckleyUniversity of Tennessee Health Science Center in Memphis, TN, USA.
Ayman H FanousDepartment of Psychiatry, University of Arizona College of Medicine, Phoenix, AZ, USA.ORCID 0009-0009-8121-9111 Humberto NicoliniDepartamento de Psiquiatría, Ciudad de México, Grupo Médico Carracci, Ciudad de Mexico, MX.ORCID 0000-0003-2494-0067 Mark H RapaportHuntsman Mental Health Institute, Department of Psychiatry, University of Utah, Salt Lake City, UT, USA.
GPC Investigators
Kenneth S KendlerDept. of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8689-6570 Carlos PatoDepartment of Psychiatry, Rutgers University, Piscataway, NJ, USA.
Tim B BigdeliInstitute for Genomics in Health, Department of Psychiatry and Behavioral Sciences, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.ORCID 0000-0003-2215-5946 Funding
Large Scale Sequencing and Analysis of GenomesU54HG003067 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GABRIEL, STACEY, LANDER, ERIC S · 2004 to 2015
$568.6MAfrican Ancestry Genomic Psychiatry CohortR01MH104964 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI BIGDELI, TIM BERNARD, FANOUS, AYMAN H · 2015 to 2024
$16.7MGenomic Psychiatry CohortR01MH085548 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PATO, CARLOS N, PATO, MICHELE T · 2008 to 2012
$16.3MWhole Genome Sequencing for Schizophrenia and Bipolar Disorder in the GPCU01MH105641 · NIMH · BROAD INSTITUTE, INC. · PI MCCARROLL, STEVEN ANDREW · 2014 to 2018
$13.6MInternational Cohort Collection for Bipolar DisorderR01MH085542 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SMOLLER, JORDAN W · 2008 to 2012
$10.7MLatino Ancestry Genomic Psychiatry CohortR01MH123451 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI BIGDELI, TIM BERNARD, FANOUS, AYMAN H · 2020 to 2025
$7.1MDiscovery of Genetic Variation Influencing Schizophrenia Using Next Generation DNR01MH086873 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KNOWLES, JAMES A · 2010 to 2014
$3.3MWhole Genome Sequencing for Schizophrenia and Bipolar Disorder in the GPCU01MH105653 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOEHNKE, MICHAEL L · 2014 to 2018
$2.8M3/3 - Whole Genome Sequencing for Schizophrenia and Bipolar Disorder in the GPCU01MH105573 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PATO, CARLOS N · 2014 to 2018
$851kGenetic architecture of transdiagnostic psychosis symptom dimensionsK01MH131847 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI Dana Lapato · 2023 to 2026
$632kNHGRI NIH HHS U54 HG003067NIMH NIH HHS K01 MH131847NIMH NIH HHS R01 MH085542NIMH NIH HHS R01 MH085548NIMH NIH HHS R01 MH086873NIMH NIH HHS R01 MH104964NIMH NIH HHS R01 MH123451NIMH NIH HHS U01 MH105573NIMH NIH HHS U01 MH105641NIMH NIH HHS U01 MH105653
6 · The paper itselfAbstract
Data-driven phenotypes have the potential to accelerate biomedical research but must be vetted thoroughly for robustness, interpretability, and generalizability. This study sought to create and evaluate the predictive validity of empirical phenotypes derived from assessments of signs and symptoms of psychopathology collected in a large cohort of patients using a validated semi-structured clinical interview based on the OPCRIT system. Data was available for N = 17,719 individuals diagnosed with schizophrenia (n = 10,429; 30% female), bipolar I disorder (n = 4,520; 53% female), or schizoaffective disorder (n = 2,770; 44% female) using DSM-IV-TR criteria. The best-fitting latent class analysis (LCA) model was a 6-class solution. Three of the six class profiles replicated results from previous studies. Stratifying by sex did not alter class profiles. Latent classes were significantly associated with established DSM diagnoses for primary and sex-stratified results but not for the LCA solution based primarily on symptoms and lacking indicators related to illness course and relative prevalence of psychotic versus affective symptoms in the overall clinical presentation. All LCAs (i.e., primary, sex-stratified, and symptom-only analyses) produced latent classes that showed statistically significant associations with demographic, etiological, and clinical correlates, but the effect sizes were modest for most associations and comparable in magnitude to those observed for established DSM diagnosis. These results collectively suggest that symptom-based empirical phenotypes derived from LCA may not outperform DSM diagnoses and reaffirm the long-observed importance of illness course for differentiating schizophrenia and bipolar I disorder.
Indexed as
Genomic Psychiatry Cohortlatent class analysisPsychosisreplication
Identifiers
PMID41282810
PMCPMC12636642
What OpenQuestion holds
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