TY - JOUR
T1 - Longitudinal clinical and functional outcome in distinct cognitive subgroups of first-episode psychosis
T2 - a cluster analysis
AU - Oomen, Priscilla P.
AU - Begemann, Marieke J. H.
AU - Brand, Bodyl A.
AU - de Haan, Lieuwe
AU - Veling, Wim
AU - Koops, Sanne
AU - van Os, Jim
AU - Smit, Filip
AU - Bakker, P. Roberto
AU - van Beveren, Nico
AU - Boonstra, Nynke
AU - Guloksuz, Sinan
AU - Kikkert, Martijn
AU - Lokkerbol, Joran
AU - Marcelis, Machteld
AU - Rosema, Bram-Sieben
AU - de Beer, Franciska
AU - Gangadin, Shiral S.
AU - Geraets, Chris N. W.
AU - van't Hag, Erna
AU - Haveman, Yudith
AU - van der Heijden, Inge
AU - Voppel, Alban E.
AU - Willemse, Elske
AU - van Amelsvoort, Therese
AU - Bak, Maarten
AU - Batalla, Albert
AU - Been, Agaath
AU - van den Bosch, Marinte
AU - van den Brink, Truus
AU - Faber, Gunnar
AU - Grootens, Koen P.
AU - de Jonge, Martin
AU - Knegtering, Rikus
AU - Kurkamp, Jorg
AU - Mahabir, Amrita
AU - Pijnenborg, Gerdina H. M.
AU - Staring, Tonnie
AU - Veen, Natalie
AU - Veerman, Selene
AU - Wiersma, Sybren
AU - Graveland, Ellen
AU - Hoornaar, Joelle
AU - Sommer, Iris E. C.
N1 - Funding Information:
The HAMLETT study is funded by ZonMW in the Netherlands (grant number 80-84800-98-41015). The funders have no role in the study design, collection, management, analysis and interpretation of data, writing the report, or the decision to submit the report for publication.
Publisher Copyright:
Copyright © The Author(s), 2021. Published by Cambridge University Press.
PY - 2023/4/19
Y1 - 2023/4/19
N2 - Background Cognitive deficits may be characteristic for only a subgroup of first-episode psychosis (FEP) and the link with clinical and functional outcomes is less profound than previously thought. This study aimed to identify cognitive subgroups in a large sample of FEP using a clustering approach with healthy controls as a reference group, subsequently linking cognitive subgroups to clinical and functional outcomes.
Methods 204 FEP patients were included. Hierarchical cluster analysis was performed using baseline brief assessment of cognition in schizophrenia (BACS). Cognitive subgroups were compared to 40 controls and linked to longitudinal clinical and functional outcomes (PANSS, GAF, self-reported WHODAS 2.0) up to 12-month follow-up.
Results Three distinct cognitive clusters emerged: relative to controls, we found one cluster with preserved cognition (n = 76), one moderately impaired cluster (n = 74) and one severely impaired cluster (n = 54). Patients with severely impaired cognition had more severe clinical symptoms at baseline, 6- and 12-month follow-up as compared to patients with preserved cognition. General functioning (GAF) in the severely impaired cluster was significantly lower than in those with preserved cognition at baseline and showed trend-level effects at 6- and 12-month follow-up. No significant differences in self-reported functional outcome (WHODAS 2.0) were present. Conclusions Current results demonstrate the existence of three distinct cognitive subgroups, corresponding with clinical outcome at baseline, 6- and 12-month follow-up. Importantly, the cognitively preserved subgroup was larger than the severely impaired group. Early identification of discrete cognitive profiles can offer valuable information about the clinical outcome but may not be relevant in predicting self-reported functional outcomes.
AB - Background Cognitive deficits may be characteristic for only a subgroup of first-episode psychosis (FEP) and the link with clinical and functional outcomes is less profound than previously thought. This study aimed to identify cognitive subgroups in a large sample of FEP using a clustering approach with healthy controls as a reference group, subsequently linking cognitive subgroups to clinical and functional outcomes.
Methods 204 FEP patients were included. Hierarchical cluster analysis was performed using baseline brief assessment of cognition in schizophrenia (BACS). Cognitive subgroups were compared to 40 controls and linked to longitudinal clinical and functional outcomes (PANSS, GAF, self-reported WHODAS 2.0) up to 12-month follow-up.
Results Three distinct cognitive clusters emerged: relative to controls, we found one cluster with preserved cognition (n = 76), one moderately impaired cluster (n = 74) and one severely impaired cluster (n = 54). Patients with severely impaired cognition had more severe clinical symptoms at baseline, 6- and 12-month follow-up as compared to patients with preserved cognition. General functioning (GAF) in the severely impaired cluster was significantly lower than in those with preserved cognition at baseline and showed trend-level effects at 6- and 12-month follow-up. No significant differences in self-reported functional outcome (WHODAS 2.0) were present. Conclusions Current results demonstrate the existence of three distinct cognitive subgroups, corresponding with clinical outcome at baseline, 6- and 12-month follow-up. Importantly, the cognitively preserved subgroup was larger than the severely impaired group. Early identification of discrete cognitive profiles can offer valuable information about the clinical outcome but may not be relevant in predicting self-reported functional outcomes.
UR - https://www.scopus.com/pages/publications/85124477366
U2 - 10.1017/S0033291721004153
DO - 10.1017/S0033291721004153
M3 - Article
C2 - 34664546
SN - 0033-2917
VL - 53
SP - 2317
EP - 2327
JO - Psychological Medicine
JF - Psychological Medicine
IS - 6
ER -