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Neural changes associated with appetite information processing in schizophrenic patients after 16 weeks of olanzapine
1Department of Psychiatry, Université de Montréal, Montréal, QC, Canada. emmanuel.stip@umontreal.ca
Abstract:
There is evidence that some atypical antipsychotics, including olanzapine, can produce unwanted metabolic side effects, weight gain and diabetes. However, neuronal correlates of change related to food information processing have not been investigated with these medications. We studied the effect of a pharmacological manipulation with an antipsychotic known to cause weight gain on metabolites, cognitive tasks and neural correlates related to food regulation. We used functional magnetic resonance imaging in conjunction with a task requiring visual processing of appetitive stimuli in schizophrenic patients and healthy controls before and after 16 weeks of antipsychotic medication with olanzapine. In patients, the psychological and neuronal changes associated following the treatment correlated with appetite control measures and metabolite levels in fasting blood samples. After 16 weeks of olanzapine treatment, the patients gained weight, increased their waist circumference, had fewer positive schizophrenia symptoms, a reduced ghrelin plasma concentration and an increased concentration of triglycerides, insulin and leptin. In premotor area, somatosensory cortices as well as bilaterally in the fusiform gyri, the olanzapine treatment increased the neural activity related to appetitive information in schizophrenic patients to similar levels relative to healthy individuals. However, a higher increase in sensitivity to appetitive stimuli after the treatment was observed in insular cortices, amygdala and cerebellum in schizophrenic patients as compared with healthy controls. Furthermore, these changes in neuronal activity correlated with changes in some metabolites and cognitive measurements related to appetite regulation.
Insights
Olanzapine treatment in schizophrenia patients led to weight gain and altered brain activity in response to food cues. These neural changes correlated with metabolic shifts and appetite regulation measures, offering insights into antipsychotic side effects.
Area of Science:
- Neuroscience
- Metabolic Psychiatry
- Pharmacology
Background:
- Atypical antipsychotics like olanzapine are linked to metabolic side effects, including weight gain and diabetes.
- Neuronal processing of food-related information during antipsychotic treatment remains understudied.
Purpose of the Study:
- To investigate the impact of olanzapine on metabolic profiles, cognitive functions, and brain activity related to food regulation in schizophrenia patients.
- To explore the correlation between neural changes, metabolic alterations, and appetite control.
Main Methods:
- Functional magnetic resonance imaging (fMRI) was used to assess brain activity during a visual food stimuli task.
- Schizophrenia patients and healthy controls were scanned before and after 16 weeks of olanzapine treatment.
- Metabolic markers (ghrelin, triglycerides, insulin, leptin) and cognitive measures were assessed.
Main Results:
- Olanzapine treatment resulted in weight gain, increased waist circumference, and reduced positive schizophrenia symptoms.
- Patients showed altered plasma concentrations of ghrelin, triglycerides, insulin, and leptin.
- Neural activity in response to appetitive stimuli increased in premotor, somatosensory, and fusiform areas, normalizing to healthy control levels.
- Increased sensitivity to appetitive stimuli was observed in the insular cortex, amygdala, and cerebellum in patients post-treatment.
- Neural and metabolic changes correlated with appetite regulation measures.
Conclusions:
- Olanzapine treatment significantly impacts brain activity related to food cue processing and metabolic parameters in schizophrenia patients.
- The observed neural alterations in response to food stimuli may contribute to the metabolic side effects associated with olanzapine.
- Findings highlight the complex interplay between antipsychotic medication, brain function, metabolism, and appetite regulation.
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