TY - JOUR
T1 - Depressive symptomatology in the first-episode schizophrenia spectrum disorders OPTiMiSE trial
T2 - prevalence, correlates, symptom progression and outcomes
AU - Lopez-Morinigo, Javier-David
AU - Fraguas, David
AU - Diaz-Caneja, Covadonga M
AU - Galvañ, Joaquin
AU - Berger, Gregor
AU - Leucht, Stefan
AU - Rossum, Inge Winter-van
AU - Arango, Celso
AU - Moreno, Carmen
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/11/13
Y1 - 2025/11/13
N2 - Numerous aspects of depressive symptomatology in first-episode schizophrenia spectrum disorders (FES) remain unclear. Based on data from the FES OPTiMiSE trial, we estimated the prevalence of depression (Calgary Depression Scale for Schizophrenia (CDSS) total score ≥7) at baseline (n = 122, 27.5%) and at weeks 4 (n = 57, 15.9%) and 10 (n = 14, 21.5%). Baseline depression was cross-sectionally associated with more severe extrapyramidal symptoms (p = 0.036) and poorer subjective wellbeing (p < 0.001). At week 4, baseline depression was linked to poorer psychosocial functioning (p < 0.001) and subjective wellbeing (p < 0.001). At week 10, baseline depression was associated with psychosis non-remission (p = 0.042) and worse subjective wellbeing (p = 0.011). There was a significant correlation between decrease in CDSS and PANSS total scores (p < 0.001) at weeks 4 and 10. Depressive symptomatology in the FES OPTiMiSE trial was prevalent and associated with poorer objectively- and subjectively-measured outcomes over a 10-week follow-up. Early intervention for depression may improve outcomes in FES.
AB - Numerous aspects of depressive symptomatology in first-episode schizophrenia spectrum disorders (FES) remain unclear. Based on data from the FES OPTiMiSE trial, we estimated the prevalence of depression (Calgary Depression Scale for Schizophrenia (CDSS) total score ≥7) at baseline (n = 122, 27.5%) and at weeks 4 (n = 57, 15.9%) and 10 (n = 14, 21.5%). Baseline depression was cross-sectionally associated with more severe extrapyramidal symptoms (p = 0.036) and poorer subjective wellbeing (p < 0.001). At week 4, baseline depression was linked to poorer psychosocial functioning (p < 0.001) and subjective wellbeing (p < 0.001). At week 10, baseline depression was associated with psychosis non-remission (p = 0.042) and worse subjective wellbeing (p = 0.011). There was a significant correlation between decrease in CDSS and PANSS total scores (p < 0.001) at weeks 4 and 10. Depressive symptomatology in the FES OPTiMiSE trial was prevalent and associated with poorer objectively- and subjectively-measured outcomes over a 10-week follow-up. Early intervention for depression may improve outcomes in FES.
U2 - 10.1038/s41537-025-00681-3
DO - 10.1038/s41537-025-00681-3
M3 - Review article
C2 - 41233335
SN - 2754-6993
VL - 11
JO - Schizophrenia
JF - Schizophrenia
IS - 1
M1 - 135
ER -