[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.146.179.146. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Original Investigation
Meta-analysis
February 2016

Heterogeneity of Psychosis Risk Within Individuals at Clinical High RiskA Meta-analytical Stratification

Author Affiliations
  • 1Institute of Psychiatry, Psychology, and Neuroscience, King’s College, London, United Kingdom
  • 2OASIS Clinic, South London and Maudsley National Health Service Foundation Trust, London, United Kingdom
  • 3Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy
  • 4University of Basel Psychiatric Clinics, Basel, Switzerland
  • 5Department of Psychiatry, Yale University, New Haven, Connecticut
  • 6Department of Psychiatry, University of Calgary, Calgary, Alberta, Canada
  • 7Orygen, the National Centre of Excellence in Youth Mental Health, and Centre for Youth Mental Health, the University of Melbourne, Parkville, Australia
  • 8Department of Psychiatry, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands
  • 9Specialized Early Psychosis Outpatient Service for Adolescents and Young Adults, Department of Psychiatry, Bruderholz, Switzerland.
  • 10Department of Neuropsychiatry, Toho University School of Medicine, Tokyo, Japan
  • 11Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea
  • 12Kwai Chung Hospital, New Territories, Hong Kong, People’s Republic of China
  • 13Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom
  • 14Nyiro Gyula Hospital, National Institute of Psychiatry and Addictions, Budapest, Hungary
  • 15Centre for Social Psychiatry, Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital of Psychiatry Zurich, Zurich, Switzerland
  • 16Department of General Psychiatry, Institute of Mental Health, Singapore, Singapore
  • 17Department of Psychiatry, Corporacio Sanitaria Parc Tauli Sabadell, Barcelona, Spain
  • 18Department of Clinical Child and Adolescent Studies, Leiden University, Leiden, the Netherlands
  • 19Department of Psychiatry, Yonsei University College of Medicine, Severance Hospital, Seoul, South Korea
  • 20Department of Psychiatry, National Taiwan University Hospital and College of Medicine, National Taiwan University, Taipei, Taiwan
  • 21Center for Psychiatric Research, Maine Medical Center, Portland, Maine
  • 22Departments of Psychiatry, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts
  • 23Psychiatry Department, University Hospital Farhat Hached, Sousse, Tunisia
  • 24Department of Psychiatry, Columbia University, New York, New York
  • 25Institute of Brain, Behaviour and Mental Health, University of Manchester, and Greater Manchester West National Health Service Mental Health Foundation Trust, Manchester, United Kingdom
JAMA Psychiatry. 2016;73(2):113-120. doi:10.1001/jamapsychiatry.2015.2324
Abstract

Importance  Individuals can be classified as being at clinical high risk (CHR) for psychosis if they meet at least one of the ultra–high-risk (UHR) inclusion criteria (brief limited intermittent psychotic symptoms [BLIPS] and/or attenuated psychotic symptoms [APS] and/or genetic risk and deterioration syndrome [GRD]) and/or basic symptoms [BS]. The meta-analytical risk of psychosis of these different subgroups is still unknown.

Objective  To compare the risk of psychosis in CHR individuals who met at least one of the major inclusion criteria and in individuals not at CHR for psychosis (CHR−).

Data Sources  Electronic databases (Web of Science, MEDLINE, Scopus) were searched until June 18, 2015, along with investigation of citations of previous publications and a manual search of the reference lists of retrieved articles.

Study Selection  We included original follow-up studies of CHR individuals who reported the risk of psychosis classified according to the presence of any BLIPS, APS and GRD, APS alone, GRD alone, BS, and CHR−.

Data Extraction and Synthesis  Independent extraction by multiple observers and random-effects meta-analysis of proportions. Moderators were tested with meta-regression analyses (Bonferroni corrected). Heterogeneity was assessed with the I2 index. Sensitivity analyses tested robustness of results. Publication biases were assessed with funnel plots and the Egger test.

Main Outcomes and Measures  The proportion of each subgroup with any psychotic disorder at 6, 12, 24, 36, and 48 or more months of follow-up.

Results  Thirty-three independent studies comprising up to 4227 individuals were included. The meta-analytical proportion of individuals meeting each UHR subgroup at intake was: 0.85 APS (95%CI, 0.79-0.90), 0.1 BLIPS (95%CI, 0.06-0.14), and 0.05 GRD (95%CI, 0.03-0.07). There were no significant differences in psychosis risk at any time point between the APS and GRD and the APS-alone subgroups. There was a higher risk of psychosis in the any BLIPS greater than APS greater than GRD-alone subgroups at 24, 36, and 48 or more months of follow-up. There was no evidence that the GRD subgroup has a higher risk of psychosis than the CHR− subgroup. There were too few BS or BS and UHR studies to allow robust conclusions.

Conclusions and Relevance  There is meta-analytical evidence that BLIPS represents separate risk subgroup compared with the APS. The GRD subgroup is infrequent and not associated with an increased risk of psychosis. Future studies are advised to stratify their findings across these different subgroups. The CHR guidelines should be updated to reflect these differences.

×