The characteristics and clinical outcomes of a pluripotent high-risk group with the potential to develop a diverse range of psychiatric disorders
- Authors
- Lee, Tae Young; Lee, Hyunju; Lee, Junhee; Lee, Yunna; Rhee, Sang Jin; Park, Dong Yeon; Paek, Myung Jae; Kim, Eun Young; Kim, Euitae; Roh, Sungwon; Jung, Hee Yeon; Kim, Minah; Kim, Se Hyun; Ahn, Yong Min; Ha, Kyooseob; Kwon, Jun Soo
- Issue Date
- Jun-2024
- Publisher
- Elsevier Ltd
- Keywords
- Bipolar disorder; CHR; Clinical high-risk; Depressive disorder; Pluripotent; Psychosis; Schizophrenia; Transdiagnostic psychiatry
- Citation
- Journal of Psychiatric Research, v.174, pp 237 - 244
- Pages
- 8
- Indexed
- SCIE
SSCI
SCOPUS
- Journal Title
- Journal of Psychiatric Research
- Volume
- 174
- Start Page
- 237
- End Page
- 244
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211732
- DOI
- 10.1016/j.jpsychires.2024.04.012
- ISSN
- 0022-3956
1879-1379
- Abstract
- Background: Recent studies have indicated that clinical high risk for psychosis (CHR-P) is highly specific for psychotic disorders other than pluripotential to various serious mental illnesses. However, not all CHR-P develop psychotic disorder only, and psychosis can occur in non-psychotic disorders as well. Our prospective cohort study aims to investigate the characteristics and clinical outcomes of a pluripotent high-risk group with the potential to develop a diverse range of psychiatric disorders. Methods: The SPRIM study is a prospective naturalistic cohort program that focuses on the early detection of those at risk of developing serious mental illness, including psychosis (CHR-P), bipolar (CHR-B), and depressive disorder (CHR-D), as well as undifferentiated risk participants (UCHR). Our study has a longitudinal design with a baseline assessment and eight follow-up evaluations at 6, 12, 18, 24, 30, 36, 42, and 48 months to determine whether participants have transitioned to psychosis or mood disorders. Results: The SPRIM sample consisted of 90 CHR participants. The total cumulative incidence rate of transition was 53.3% (95% CI 32.5–77.2). CHR-P, CHR-B, CHR-D, and UCHR had cumulative incidence rates of 13.7% (95% CI 3.4–46.4), 52.4% (95% CI 28.1–81.1), 66.7% (95% CI 24.6–98.6) and 54.3% (95% CI 20.5–93.1), respectively. The cumulative incidence of psychosis, bipolar, and depressive disorder among all participants was 3.3% (95% CI 0.8–11.5), 45.7% (95% CI 24.4–73.6), and 11.2% (95% CI 3.1–36.2), respectively. Conclusions: Our study suggests that the concept of pluripotent high-risk for a diverse range of psychiatric disorders is an integrative approach to examining transdiagnostic interactions between illnesses with a high transition rate and minimizing stigma.
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