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Author Notes:

Corresponding Author: Arthur T. Ryan, 36 Eagle Row, #270, Atlanta GA 30307, Tel: 404-727-7547, Fax: 404-727-1284, arthur.t.ryan@gmail.com

Dr. Arthur Ryan undertook the statistical analysis and wrote the first draft of the manuscript.

Dr. Elaine Walker was involved in the writing of subsequent drafts of the manuscript.

All of the authors listed were involved in study design and have contributed to and approved the final manuscript.

We thank Dr. John Hanfelt for reviewing an early version of the analyses for this paper and providing helpful feedback.

There are no conflicts of interest for any of the authors with respect to the data in this paper or for the study.

Subject:

Research Funding:

This work was supported by a collaborative U01 award from the National Institute of Mental Health at the National Institutes of Health (MH081902 to TDC; MH081857 to BAC; MH081988 to EW; MH081928 to LJS; MH082004 to DP; MH082022 to KC; MH081984 to JA; MH082022 to SWW) and NIMH P50 MH066286 and Staglin Music Festival for Mental Health (CEB), NIMH P50 MH080272, and the Commonwealth of Massachusetts (SCDMH82101008006) to LJS.

AR is supported by the Department of Veterans Affairs Office of Academic Affiliations Advanced Fellowship Program in Mental Illness Research and Treatment. His work was supported with resources and the use of facilities at the VA Capitol Health Care Network (VISN 5) MIRECC and the University of Maryland School of Medicine Department of Psychiatry.

Keywords:

  • schizophrenia
  • prodrome
  • finite mixture models
  • disorganized symptoms
  • heterogeneity

Latent class cluster analysis of symptom ratings identifies distinct subgroups within the clinical high risk for psychosis syndrome

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Journal Title:

Schizophrenia Research

Volume:

Volume 197

Publisher:

, Pages 522-530

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The clinical-high-risk for psychosis (CHR-P) syndrome is heterogeneous in terms of clinical presentation and outcomes. Identifying more homogenous subtypes of the syndrome may help clarify its etiology and improve the prediction of psychotic illness. This study applied latent class cluster analysis (LCCA) to symptom ratings from the North American Prodrome Longitudinal Studies 1 and 2 (NAPLS 1 and 2). These analyses produced evidence for three to five subgroups within the CHR-P syndrome. Differences in negative and disorganized symptoms distinguished among the subgroups. Subgroup membership was found to predict conversion to psychosis. The authors contrast the methods employed within this study with previous attempts to identify more homogenous subgroups of CHR-P individuals and discuss how these results could be tested in future samples of CHR-P individuals.

Copyright information:

© 2017

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