TY - JOUR
T1 - Relationship between jumping to conclusions and clinical outcomes in people at clinical high-risk for psychosis
AU - Catalan, Ana
AU - Tognin, Stefania
AU - Kempton, Matthew J
AU - Stahl, Daniel
AU - Salazar de Pablo, Gonzalo
AU - Nelson, Barnaby
AU - Pantelis, Christos
AU - Riecher-Rössler, Anita
AU - Bressan, Rodrigo
AU - Barrantes-Vidal, Neus
AU - Krebs, Marie-Odile
AU - Nordentoft, Merete
AU - Ruhrmann, Stephan
AU - Sachs, Gabriele
AU - Rutten, Bart P F
AU - van Os, Jim
AU - de Haan, Lieuwe
AU - van der Gaag, Mark
AU - Valmaggia, Lucia R
AU - McGuire, Philip
N1 - Funding Information:
We would like to thank all participants who took part in the study. This work was supported by the European Network of National Schizophrenia Networks Studying Gene–Environment Interactions (EU-GEI) Project is funded by grant agreement HEALTH-F2-20010–241909; [Project EU-GEI] from the European Community's Seventh Framework Programme. Additional support was provided by a Medical Research Council Fellowship to M Kempton (grant MR/J008915/1). N Barrantes-Vidal received additional support from the Ministerio de Ciencia, Innovación e Universidades (PSI2017-87512-C2-1-R) and the Generalitat de Catalunya (2017SGR1612 and ICREA Academia Award). The study received financial support by French Health Ministry (PHRC, AOM-07-118, ‘Influence of cannabis psychopathological outcome in At-risk mental state’ (ICAAR study)) et de la Fondation pour la Recherche Médicale (fellowship OG). Sainte-Anne Hospital promoted the study. D Stahl was part-funded by the National Institute for Health Research (NIHR) Maudsley Biomedical Research Centre at South London Maudsley Foundation Trust and King's College London. The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care. C Pantelis was supported by an Australian National Health & Medical Research Council (NHMRC) Senior Principal Research Fellowship (1105825).
Publisher Copyright:
Copyright © The Author(s), 2020. Published by Cambridge University Press.
PY - 2022/6
Y1 - 2022/6
N2 - Background Psychosis is associated with a reasoning bias, which manifests as a tendency to 'jump to conclusions'. We examined this bias in people at clinical high-risk for psychosis (CHR) and investigated its relationship with their clinical outcomes. Methods In total, 303 CHR subjects and 57 healthy controls (HC) were included. Both groups were assessed at baseline, and after 1 and 2 years. A 'beads' task was used to assess reasoning bias. Symptoms and level of functioning were assessed using the Comprehensive Assessment of At-Risk Mental States scale (CAARMS) and the Global Assessment of Functioning (GAF), respectively. During follow up, 58 (16.1%) of the CHR group developed psychosis (CHR-T), and 245 did not (CHR-NT). Logistic regressions, multilevel mixed models, and Cox regression were used to analyse the relationship between reasoning bias and transition to psychosis and level of functioning, at each time point. Results There was no association between reasoning bias at baseline and the subsequent onset of psychosis. However, when assessed after the transition to psychosis, CHR-T participants showed a greater tendency to jump to conclusions than CHR-NT and HC participants (55, 17, 17%; χ2 = 8.13, p = 0.012). There was a significant association between jumping to conclusions (JTC) at baseline and a reduced level of functioning at 2-year follow-up in the CHR group after adjusting for transition, gender, ethnicity, age, and IQ. Conclusions In CHR participants, JTC at baseline was associated with adverse functioning at the follow-up. Interventions designed to improve JTC could be beneficial in the CHR population.
AB - Background Psychosis is associated with a reasoning bias, which manifests as a tendency to 'jump to conclusions'. We examined this bias in people at clinical high-risk for psychosis (CHR) and investigated its relationship with their clinical outcomes. Methods In total, 303 CHR subjects and 57 healthy controls (HC) were included. Both groups were assessed at baseline, and after 1 and 2 years. A 'beads' task was used to assess reasoning bias. Symptoms and level of functioning were assessed using the Comprehensive Assessment of At-Risk Mental States scale (CAARMS) and the Global Assessment of Functioning (GAF), respectively. During follow up, 58 (16.1%) of the CHR group developed psychosis (CHR-T), and 245 did not (CHR-NT). Logistic regressions, multilevel mixed models, and Cox regression were used to analyse the relationship between reasoning bias and transition to psychosis and level of functioning, at each time point. Results There was no association between reasoning bias at baseline and the subsequent onset of psychosis. However, when assessed after the transition to psychosis, CHR-T participants showed a greater tendency to jump to conclusions than CHR-NT and HC participants (55, 17, 17%; χ2 = 8.13, p = 0.012). There was a significant association between jumping to conclusions (JTC) at baseline and a reduced level of functioning at 2-year follow-up in the CHR group after adjusting for transition, gender, ethnicity, age, and IQ. Conclusions In CHR participants, JTC at baseline was associated with adverse functioning at the follow-up. Interventions designed to improve JTC could be beneficial in the CHR population.
KW - Functioning
KW - Psychosis
KW - Transition to psychosis
KW - Ultra high-risk
UR - http://www.scopus.com/inward/record.url?scp=85092600075&partnerID=8YFLogxK
U2 - 10.1017/S0033291720003396
DO - 10.1017/S0033291720003396
M3 - Article
C2 - 33019957
SN - 0033-2917
VL - 52
SP - 1569
EP - 1577
JO - Psychological medicine
JF - Psychological medicine
IS - 8
ER -