TY - JOUR
T1 - Intracranial and subcortical volumes in adolescents with early-onset psychosis
T2 - A multisite mega-analysis from the ENIGMA consortium
AU - For the ENIGMA-EOP Working Group
AU - Gurholt, Tiril P.
AU - Lonning, Vera
AU - Nerland, Stener
AU - Jørgensen, Kjetil N.
AU - Haukvik, Unn K.
AU - Alloza, Clara
AU - Arango, Celso
AU - Barth, Claudia
AU - Bearden, Carrie E.
AU - Berk, Michael
AU - Bohman, Hannes
AU - Dandash, Orwa
AU - Díaz-Caneja, Covadonga M.
AU - Edbom, Carl T.
AU - van Erp, Theo G.M.
AU - Fett, Anne Kathrin J.
AU - Frangou, Sophia
AU - Goldstein, Benjamin I.
AU - Grigorian, Anahit
AU - Jahanshad, Neda
AU - James, Anthony C.
AU - Janssen, Joost
AU - Johannessen, Cecilie
AU - Karlsgodt, Katherine H.
AU - Kempton, Matthew J.
AU - Kochunov, Peter
AU - Krabbendam, Lydia
AU - Kyriakopoulos, Marinos
AU - Lundberg, Mathias
AU - MacIntosh, Bradley J.
AU - Rund, Bjørn Rishovd
AU - Smelror, Runar E.
AU - Sultan, Alysha
AU - Tamnes, Christian K.
AU - Thomopoulos, Sophia I.
AU - Vajdi, Ariana
AU - Wedervang-Resell, Kirsten
AU - Myhre, Anne M.
AU - Andreassen, Ole A.
AU - Thompson, Paul M.
AU - Agartz, Ingrid
N1 - Publisher Copyright:
© 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
PY - 2022/1
Y1 - 2022/1
N2 - Early-onset psychosis disorders are serious mental disorders arising before the age of 18 years. Here, we investigate the largest neuroimaging dataset, to date, of patients with early-onset psychosis and healthy controls for differences in intracranial and subcortical brain volumes. The sample included 263 patients with early-onset psychosis (mean age: 16.4 ± 1.4 years, mean illness duration: 1.5 ± 1.4 years, 39.2% female) and 359 healthy controls (mean age: 15.9 ± 1.7 years, 45.4% female) with magnetic resonance imaging data, pooled from 11 clinical cohorts. Patients were diagnosed with early-onset schizophrenia (n = 183), affective psychosis (n = 39), or other psychotic disorders (n = 41). We used linear mixed-effects models to investigate differences in intracranial and subcortical volumes across the patient sample, diagnostic subgroup and antipsychotic medication, relative to controls. We observed significantly lower intracranial (Cohen's d = −0.39) and hippocampal (d = −0.25) volumes, and higher caudate (d = 0.25) and pallidum (d = 0.24) volumes in patients relative to controls. Intracranial volume was lower in both early-onset schizophrenia (d = −0.34) and affective psychosis (d = −0.42), and early-onset schizophrenia showed lower hippocampal (d = −0.24) and higher pallidum (d = 0.29) volumes. Patients who were currently treated with antipsychotic medication (n = 193) had significantly lower intracranial volume (d = −0.42). The findings demonstrate a similar pattern of brain alterations in early-onset psychosis as previously reported in adult psychosis, but with notably low intracranial volume. The low intracranial volume suggests disrupted neurodevelopment in adolescent early-onset psychosis.
AB - Early-onset psychosis disorders are serious mental disorders arising before the age of 18 years. Here, we investigate the largest neuroimaging dataset, to date, of patients with early-onset psychosis and healthy controls for differences in intracranial and subcortical brain volumes. The sample included 263 patients with early-onset psychosis (mean age: 16.4 ± 1.4 years, mean illness duration: 1.5 ± 1.4 years, 39.2% female) and 359 healthy controls (mean age: 15.9 ± 1.7 years, 45.4% female) with magnetic resonance imaging data, pooled from 11 clinical cohorts. Patients were diagnosed with early-onset schizophrenia (n = 183), affective psychosis (n = 39), or other psychotic disorders (n = 41). We used linear mixed-effects models to investigate differences in intracranial and subcortical volumes across the patient sample, diagnostic subgroup and antipsychotic medication, relative to controls. We observed significantly lower intracranial (Cohen's d = −0.39) and hippocampal (d = −0.25) volumes, and higher caudate (d = 0.25) and pallidum (d = 0.24) volumes in patients relative to controls. Intracranial volume was lower in both early-onset schizophrenia (d = −0.34) and affective psychosis (d = −0.42), and early-onset schizophrenia showed lower hippocampal (d = −0.24) and higher pallidum (d = 0.29) volumes. Patients who were currently treated with antipsychotic medication (n = 193) had significantly lower intracranial volume (d = −0.42). The findings demonstrate a similar pattern of brain alterations in early-onset psychosis as previously reported in adult psychosis, but with notably low intracranial volume. The low intracranial volume suggests disrupted neurodevelopment in adolescent early-onset psychosis.
KW - adolescence
KW - antipsychotics
KW - brain structure
KW - early-onset
KW - intracranial volume
KW - psychosis spectrum
UR - http://www.scopus.com/inward/record.url?scp=85092162259&partnerID=8YFLogxK
U2 - 10.1002/hbm.25212
DO - 10.1002/hbm.25212
M3 - Article
C2 - 33017498
AN - SCOPUS:85092162259
SN - 1065-9471
VL - 43
SP - 373
EP - 384
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 1
ER -