TY - JOUR
T1 - Influence of cannabis use on incidence of psychosis in people at clinical high risk
AU - Chester, Lucy A.
AU - Valmaggia, Lucia R.
AU - Kempton, Matthew J.
AU - Chesney, Edward
AU - Oliver, Dominic
AU - Hedges, Emily P.
AU - Klatsa, Elise
AU - Stahl, Daniel
AU - van der Gaag, Mark
AU - de Haan, Lieuwe
AU - Nelson, Barnaby
AU - McGorry, Patrick
AU - Amminger, G. Paul
AU - Riecher-Rössler, Anita
AU - Studerus, Erich
AU - Bressan, Rodrigo
AU - Barrantes-Vidal, Neus
AU - Krebs, Marie-Odile
AU - Glenthøj, Birte
AU - Nordentoft, Merete
AU - Ruhrmann, Stephan
AU - Sachs, Gabriele
AU - McGuire, Philip
AU - EU-GEI High Risk Study Group
AU - McGuire, Philip
AU - Valmaggia, Lucia R.
AU - Kempton, Matthew J.
AU - Calem, Maria
AU - Tognin, Stefania
AU - Modinos, Gemma
AU - van der Gaag, Mark
AU - Velthorst, Eva
AU - Kraan, Tamar C.
AU - van Dam, Daniella S.
AU - Burger, Nadine
AU - Nelson, Barnaby
AU - McGorry, Patrick
AU - Amminger, G. Paul
AU - Pantelis, Christos
AU - Politis, Athena
AU - Goodall, Joanne
AU - Riecher-Rössler, Anita
AU - Borgwardt, Stefan
AU - Studerus, Erich
AU - Bressan, Rodrigo
AU - Gadelha, Ary
AU - Brietzke, Elisa
AU - Asevedo, Graccielle
AU - Asevedo, Elson
AU - Zugman, Andre
AU - Barrantes-Vidal, Neus
AU - Domínguez-Martínez, Tecelli
AU - Racioppi, Anna
AU - Kwapil, Thomas R.
AU - Monsonet, Manel
AU - Hinojosa, L. dia
AU - Kazes, Mathilde
AU - Daban, Claire
AU - Bourgin, Julie
AU - Gay, Olivier
AU - Mam-Lam-Fook, C. lia
AU - Krebs, Marie-Odile
AU - Nordholm, Dorte
AU - Randers, Lasse
AU - Krakauer, Kristine
AU - Glenthøj, Louise
AU - Glenthøj, Birte
AU - Nordentoft, Merete
AU - Ruhrmann, Stephan
AU - Gebhard, Dominika
AU - Arnhold, Julia
AU - Klosterkötter, Joachim
AU - Sachs, Gabriele
AU - Lasser, Iris
AU - Winklbaur, Bernadette
AU - Delespaul, Philippe A.
AU - Rutten, Bart P.
AU - van Os, Jim
N1 - Funding Information:
The European Network of National Schizophrenia Networks Studying Gene–Environment Interactions (EU‐GEI) Project is funded by grant agreement HEALTH‐F2‐2010‐241909 (Project EU‐GEI) from the European Community's Seventh Framework Programme. Additional support was provided by the NIHR Maudsley Biomedical Research Centre, an NIHR Maudsley Biomedical Research Centre PhD studentship to LC and a Medical Research Council Fellowship to MK (grant MR/J008915/1). Many thanks to the EU‐GEI High Risk Study Group for designing and implementing the study. EU‐GEI collaborators and their affiliations are listed in the Supplementary Materials, including all non‐author contributors.
Publisher Copyright:
© 2023 The Authors. Psychiatry and Clinical Neurosciences published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Psychiatry and Neurology.
PY - 2023/9
Y1 - 2023/9
N2 - Aims: Evidence for case–control studies suggests that cannabis use is a risk factor for the development of psychosis. However, there have been limited prospective studies and the direction of this association remains controversial. The primary aim of the present study was to examine the association between cannabis use and the incidence of psychotic disorders in people at clinical high risk of psychosis. Secondary aims were to assess associations between cannabis use and the persistence of psychotic symptoms, and with functional outcome. Methods: Current and previous cannabis use were assessed in individuals at clinical high risk of psychosis (n = 334) and healthy controls (n = 67), using a modified version of the Cannabis Experience Questionnaire. Participants were assessed at baseline and followed up for 2 years. Transition to psychosis and persistence of psychotic symptoms were assessed using the Comprehensive Assessment of At-Risk Mental States criteria. Level of functioning at follow up was assessed using the Global Assessment of Functioning disability scale. Results: During follow up, 16.2% of the clinical high-risk sample developed psychosis. Of those who did not become psychotic, 51.4% had persistent symptoms and 48.6% were in remission. There was no significant association between any measure of cannabis use at baseline and either transition to psychosis, the persistence of symptoms, or functional outcome. Conclusions: These findings contrast with epidemiological data that suggest that cannabis use increases the risk of psychotic disorder.
AB - Aims: Evidence for case–control studies suggests that cannabis use is a risk factor for the development of psychosis. However, there have been limited prospective studies and the direction of this association remains controversial. The primary aim of the present study was to examine the association between cannabis use and the incidence of psychotic disorders in people at clinical high risk of psychosis. Secondary aims were to assess associations between cannabis use and the persistence of psychotic symptoms, and with functional outcome. Methods: Current and previous cannabis use were assessed in individuals at clinical high risk of psychosis (n = 334) and healthy controls (n = 67), using a modified version of the Cannabis Experience Questionnaire. Participants were assessed at baseline and followed up for 2 years. Transition to psychosis and persistence of psychotic symptoms were assessed using the Comprehensive Assessment of At-Risk Mental States criteria. Level of functioning at follow up was assessed using the Global Assessment of Functioning disability scale. Results: During follow up, 16.2% of the clinical high-risk sample developed psychosis. Of those who did not become psychotic, 51.4% had persistent symptoms and 48.6% were in remission. There was no significant association between any measure of cannabis use at baseline and either transition to psychosis, the persistence of symptoms, or functional outcome. Conclusions: These findings contrast with epidemiological data that suggest that cannabis use increases the risk of psychotic disorder.
KW - THC
KW - clinical high-risk
KW - longitudinal
KW - psychotic disorders
KW - substance use
UR - https://www.scopus.com/pages/publications/85159224349
U2 - 10.1111/pcn.13555
DO - 10.1111/pcn.13555
M3 - Article
C2 - 37070555
SN - 1323-1316
VL - 77
SP - 469
EP - 477
JO - Psychiatry and clinical neurosciences
JF - Psychiatry and clinical neurosciences
IS - 9
ER -