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The hierarchical taxonomy of psychopathology in clinical high risk for psychosis: Validation and extension.
Williams, Trevor F; Williams, Alexander L; Cowan, Henry R; Walker, Elaine F; Cannon, Tyrone D; Bearden, Carrie E; Keshavan, Matcheri; Cornblatt, Barbara A; Addington, Jean; Woods, Scott W; Perkins, Diana O; Mathalon, Daniel H; Cadenhead, Kristin S; Stone, William S; Mittal, Vijay A.
Affiliation
  • Williams TF; Department of Psychology, Northwestern University.
  • Williams AL; Department of Psychology, Northwestern University.
  • Cowan HR; Ohio State University.
  • Walker EF; Department of Psychology, Emory University.
  • Cannon TD; Department of Psychology, Yale University.
  • Bearden CE; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles.
  • Keshavan M; Department of Psychiatry, Harvard Medical School, Beth Israel Deaconess Medical Center.
  • Cornblatt BA; Department of Psychiatry, Zucker Hillside Hospital.
  • Addington J; Department of Psychiatry, Hotchkiss Brain Institute, University of Calgary.
  • Woods SW; Department of Psychiatry, Yale University.
  • Perkins DO; Department of Psychiatry, University of North Carolina, Chapel Hill.
  • Mathalon DH; Department of Psychiatry, University of California San Francisco.
  • Cadenhead KS; Department of Psychiatry, University of California San Diego.
  • Stone WS; Department of Psychiatry, Harvard Medical School, Beth Israel Deaconess Medical Center.
  • Mittal VA; Department of Psychology, Northwestern University.
J Psychopathol Clin Sci ; 133(3): 235-244, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38546628
ABSTRACT
The Hierarchical Taxonomy of Psychopathology (HiTOP) consortium's transdiagnostic dimensional model of psychopathology has considerable support; however, this model has been underresearched in individuals at clinical high risk for psychosis (CHR-P), a population that may advance the model. CHR-P individuals not only have attenuated psychotic symptoms that vary in severity, but also have many comorbid diagnoses and varied clinical outcomes, including disorders with uncertain relations to HiTOP (e.g., obsessive-compulsive disorder). The present study used self-report and interview data from North American Prodrome Longitudinal Study-3 (710 CHR, 96 controls) to replicate the HiTOP model and test specific hypotheses regarding disorders with uncertain relations to its dimensions. Additionally, the present study examined the HiTOP model in relation to childhood trauma, declines in social functioning, and development of full psychosis. Confirmatory factor analysis indicated that the HiTOP model's fit was nearly adequate (e.g., comparative fit index = .89), though several theory-relevant modifications were indicated. Additionally, specific tests were conducted to gain a more fine-grained perspective on how disorders with less clear prior evidence were related to the HiTOP model. Notable findings from these analyses include bipolar spectrum disorders relating to the psychosis super spectrum (i.e., .39 loading), and obsessive-compulsive disorder showing a complex pattern of loadings (e.g., internalizing and psychosis). The final model parsimoniously accounted for childhood trauma (e.g., super spectra rs = .22-.32), associations with current functioning, and predicted future conversion to a psychotic disorder (e.g., super spectra R² = .13). Overall, these results inform the HiTOP model and suggest its promise for CHR-P research. (PsycInfo Database Record (c) 2024 APA, all rights reserved).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotic Disorders / Bipolar Disorder / Mental Disorders Limits: Humans Language: En Journal: J Psychopathol Clin Sci Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotic Disorders / Bipolar Disorder / Mental Disorders Limits: Humans Language: En Journal: J Psychopathol Clin Sci Year: 2024 Document type: Article
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