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Can We Predict Psychosis Outside the Clinical High-Risk State? A Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders.
Schizophr Bull. 2018 Feb 15; 44(2):276-285.SB

Abstract

Recent evidence has suggested that psychosis could develop not only in people at clinical high risk for psychosis (CHR-P) but also in those with clinical risk syndromes for emergent nonpsychotic mental disorders. The proportion of people with these clinical risk syndromes who will develop psychosis rather than to other nonpsychotic mental disorders is undetermined. Electronic databases were searched for studies reporting on clinical risk syndromes for the development of emergent nonpsychotic mental disorders. Incidence of emerging psychotic and nonpsychotic mental disorders defined on the ICD or DSM. Of a total of 9 studies relating to 3006 nonpsychotic at-risk individuals were included. Within prospective studies (n = 4, sample = 1051), the pooled incidence of new psychotic disorders across these clinical risk syndromes was of 12.9 per 1000 person-years (95% CI: 4.3 to 38.6) and that of nonpsychotic disorders (n = 3, sample = 538) was of 43.5 per 1000 person-years (95% CI: 30.9 to 61.3). Psychotic disorders may emerge outside the CHR-P paradigm, from clinical risk syndromes for incident nonpsychotic disorders, albeit at lower rates than in the CHR-P group. The clinical risk syndromes for emerging nonpsychotic disorders may exhibit a pluripotential risk of developing several types of mental disorders compared with CHR-P. If substantiated by future research, the current findings suggest that it may be useful to move beyond the current strategy of identifying individuals meeting CHR-P criteria only.

Authors+Show Affiliations

Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea. Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Republic of Korea.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Review
Systematic Review

Language

eng

PubMed ID

29438561

Citation

Lee, Tae Young, et al. "Can We Predict Psychosis Outside the Clinical High-Risk State? a Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders." Schizophrenia Bulletin, vol. 44, no. 2, 2018, pp. 276-285.
Lee TY, Lee J, Kim M, et al. Can We Predict Psychosis Outside the Clinical High-Risk State? A Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders. Schizophr Bull. 2018;44(2):276-285.
Lee, T. Y., Lee, J., Kim, M., Choe, E., & Kwon, J. S. (2018). Can We Predict Psychosis Outside the Clinical High-Risk State? A Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders. Schizophrenia Bulletin, 44(2), 276-285. https://doi.org/10.1093/schbul/sbx173
Lee TY, et al. Can We Predict Psychosis Outside the Clinical High-Risk State? a Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders. Schizophr Bull. 2018 02 15;44(2):276-285. PubMed PMID: 29438561.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Can We Predict Psychosis Outside the Clinical High-Risk State? A Systematic Review of Non-Psychotic Risk Syndromes for Mental Disorders. AU - Lee,Tae Young, AU - Lee,Junhee, AU - Kim,Minah, AU - Choe,Eugenie, AU - Kwon,Jun Soo, PY - 2018/2/14/pubmed PY - 2018/11/15/medline PY - 2018/2/14/entrez SP - 276 EP - 285 JF - Schizophrenia bulletin JO - Schizophr Bull VL - 44 IS - 2 N2 - Recent evidence has suggested that psychosis could develop not only in people at clinical high risk for psychosis (CHR-P) but also in those with clinical risk syndromes for emergent nonpsychotic mental disorders. The proportion of people with these clinical risk syndromes who will develop psychosis rather than to other nonpsychotic mental disorders is undetermined. Electronic databases were searched for studies reporting on clinical risk syndromes for the development of emergent nonpsychotic mental disorders. Incidence of emerging psychotic and nonpsychotic mental disorders defined on the ICD or DSM. Of a total of 9 studies relating to 3006 nonpsychotic at-risk individuals were included. Within prospective studies (n = 4, sample = 1051), the pooled incidence of new psychotic disorders across these clinical risk syndromes was of 12.9 per 1000 person-years (95% CI: 4.3 to 38.6) and that of nonpsychotic disorders (n = 3, sample = 538) was of 43.5 per 1000 person-years (95% CI: 30.9 to 61.3). Psychotic disorders may emerge outside the CHR-P paradigm, from clinical risk syndromes for incident nonpsychotic disorders, albeit at lower rates than in the CHR-P group. The clinical risk syndromes for emerging nonpsychotic disorders may exhibit a pluripotential risk of developing several types of mental disorders compared with CHR-P. If substantiated by future research, the current findings suggest that it may be useful to move beyond the current strategy of identifying individuals meeting CHR-P criteria only. SN - 1745-1701 UR - https://www.unboundmedicine.com/medline/citation/29438561/The_Histamine_H3_Receptor:Structure_Pharmacology_and_Function DB - PRIME DP - Unbound Medicine ER -