TY - JOUR
T1 - The psychopathology and neuroanatomical markers of depression in early psychosis
AU - PRONIA Consortium
AU - Upthegrove, Rachel
AU - Lalousis, Paris Alexandros
AU - Mallikarjun, Pavan
AU - Chisholm, Katie
AU - Griffiths, Lowri
AU - Iqbal, Mariam
AU - Pelton, Mirabel
AU - Reniers, Renate
AU - Stainton, Alexandra
AU - Rosen, Marlene
AU - Ruef, A.
AU - Dwyer, Dominic
AU - Marian, Surman
AU - Penzal, Nora
AU - Kambietz, Lana
AU - Alessasandro, Bertolino
AU - Brambillo, Paolo
AU - Borgwardt, Stefan
AU - Kambietz, Joseph
AU - Lencer, Rebekka
AU - Pantelis, C
AU - Ruhrmann, S
AU - Schultze Lutter, F
AU - Salokangas, R. K.R.
AU - Meisenzahl, Eva
AU - Wood, Stephen
AU - Koutsouleris, Nikolaos
PY - 2020/7/7
Y1 - 2020/7/7
N2 - Depression frequently occurs in first-episode psychosis (FEP) and predicts longer-term negative outcomes. It is possible that this depression is seen primarily in a distinct subgroup, which if identified could allow targeted treatments. We hypothesize that patients with recent-onset psychosis (ROP) and comorbid depression would be identifiable by symptoms and neuroanatomical features similar to those seen in recent-onset depression (ROD). Data were extracted from the multisite PRONIA study: 154 ROP patients (FEP within 3 months of treatment onset), of whom 83 were depressed (ROP+D) and 71 who were not depressed (ROP−D), 146 ROD patients, and 265 healthy controls (HC). Analyses included a (1) principal component analysis that established the similar symptom structure of depression in ROD and ROP+D, (2) supervised machine learning (ML) classification with repeated nested cross-validation based on depressive symptoms separating ROD vs ROP+D, which achieved a balanced accuracy (BAC) of 51%, and (3) neuroanatomical ML-based classification, using regions of interest generated from ROD subjects, which identified BAC of 50% (no better than chance) for separation of ROP+D vs ROP−D. We conclude that depression at a symptom level is broadly similar with or without psychosis status in recent-onset disorders; however, this is not driven by a separable depressed subgroup in FEP. Depression may be intrinsic to early stages of psychotic disorder, and thus treating depression could produce widespread benefit.
AB - Depression frequently occurs in first-episode psychosis (FEP) and predicts longer-term negative outcomes. It is possible that this depression is seen primarily in a distinct subgroup, which if identified could allow targeted treatments. We hypothesize that patients with recent-onset psychosis (ROP) and comorbid depression would be identifiable by symptoms and neuroanatomical features similar to those seen in recent-onset depression (ROD). Data were extracted from the multisite PRONIA study: 154 ROP patients (FEP within 3 months of treatment onset), of whom 83 were depressed (ROP+D) and 71 who were not depressed (ROP−D), 146 ROD patients, and 265 healthy controls (HC). Analyses included a (1) principal component analysis that established the similar symptom structure of depression in ROD and ROP+D, (2) supervised machine learning (ML) classification with repeated nested cross-validation based on depressive symptoms separating ROD vs ROP+D, which achieved a balanced accuracy (BAC) of 51%, and (3) neuroanatomical ML-based classification, using regions of interest generated from ROD subjects, which identified BAC of 50% (no better than chance) for separation of ROP+D vs ROP−D. We conclude that depression at a symptom level is broadly similar with or without psychosis status in recent-onset disorders; however, this is not driven by a separable depressed subgroup in FEP. Depression may be intrinsic to early stages of psychotic disorder, and thus treating depression could produce widespread benefit.
KW - schizophrenia
KW - psychosis
KW - depression
KW - gray matter volume
KW - psychopathology
KW - machine learning
U2 - 10.1093/schbul/sbaa094
DO - 10.1093/schbul/sbaa094
M3 - Article
SN - 0586-7614
VL - 2020
JO - Schizophrenia bulletin
JF - Schizophrenia bulletin
M1 - sbaa094
ER -