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Progressive brain changes in children and adolescents with first-episode psychosis
Celso Arango1, Marta Rapado-Castro, Santiago Reig
1Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, Centro de Investigación Biomédica en Red de Salud Mental, Madrid, Spain. carango@hggm.es
Insights
Pediatric patients with schizophrenia experienced greater gray matter (GM) loss in the frontal lobe compared to controls. These progressive brain changes may indicate a poorer prognosis in early-onset psychosis.
Area of Science:
- Neuroscience
- Psychiatry
- Radiology
Background:
- Childhood-onset schizophrenia is associated with progressive gray matter (GM) loss.
- It remains unclear if pediatric patients with other psychoses share similar brain changes.
Purpose of the Study:
- To investigate the progression of brain changes in first-episode early-onset psychosis.
- To determine the relationship between these changes, diagnosis, and prognosis over a 2-year follow-up period.
Main Methods:
- A prospective, multicenter, naturalistic 2-year follow-up study.
- Involved 110 patients with early-onset psychosis and 98 healthy controls.
- Utilized magnetic resonance imaging (MRI) to assess brain gray matter (GM) and cerebrospinal fluid (CSF) volumes.
Main Results:
- Schizophrenia patients showed significantly greater GM volume loss in the frontal lobe and increased frontal CSF volume compared to controls.
- Total GM and left parietal GM changes were also significantly different in schizophrenia patients.
- No significant differences were observed in patients with bipolar disorder.
Conclusions:
- Patients with schizophrenia or other psychoses exhibit accelerated GM volume loss and CSF volume increase in the frontal lobe.
- Progressive brain changes are more pronounced in schizophrenia than in bipolar disorder.
- These observed brain volume alterations may serve as potential markers for poorer prognosis in early-onset psychosis.
Context:
Progressive loss of brain gray matter (GM) has been reported in childhood-onset schizophrenia; however, it is uncertain whether these changes are shared by pediatric patients with different psychoses.
Objective:
To examine the progression of brain changes in first-episode early-onset psychosis and their relationship to diagnosis and prognosis at 2-year follow-up.
Design:
Prospective, multicenter, naturalistic, 2-year follow-up study.
Setting:
Six child and adolescent psychiatric units in Spain.
Participants:
A total of 110 patients and 98 healthy controls were recruited between March 1, 2003, and November 31, 2005. Magnetic resonance imaging of the brain was performed for 61 patients with schizophrenia (n = 25), bipolar disorder (n = 16), or other psychoses (n = 20) and 70 controls (both at baseline and after 2 years of follow-up). Mean age at baseline was 15.5 years (patients) and 15.3 years (controls).
Main Outcome Measures:
The GM and cerebrospinal fluid (CSF) volumes in the total brain and frontal, parietal, and temporal lobes.
Results:
Compared with controls, patients with schizophrenia showed greater GM volume loss in the frontal lobe during the 2-year follow-up (left: -3.3 vs -0.6 cm(3), P = .004; right: -3.7 vs -0.8 cm(3), P = .005) and left frontal CSF volume increase (left: 6.7 vs 2.4 cm(3), P = .006). In addition to frontal volume, changes for total GM (-37.1 vs -14.5 cm(3), P = .001) and left parietal GM (-4.3 vs -2.2 cm(3), P = .04) were significantly different in schizophrenic patients compared with controls. No significant differences emerged for patients with bipolar disease. Greater left frontal GM volume loss was related to more weeks of hospitalization, whereas severity of negative symptoms correlated with CSF increase in patients with schizophrenia.
Conclusions:
Patients with schizophrenia or other psychoses showed greater loss of GM volume and increase of CSF in the frontal lobe relative to controls. Progressive changes were more evident in patients with schizophrenia than those with bipolar disorder. These changes in specific brain volumes after onset of psychotic symptoms may be related to markers of poorer prognosis.
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