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[11C]Mirtazapine binding in depressed antidepressant nonresponders studied by PET neuroimaging
Donald F Smith1, Bo S Stork, Gregers Wegener
1Center for Psychiatric Research, Psychiatric Hospital of Aarhus University, Risskov, 8240, Denmark. dfsmithdfsmith@gmail.com
Rationale:
Lack of benefit from antidepressant drug therapy is a major source of human suffering, affecting at least 25% of people with major depressive disorder. We want to know whether nonresponse to antidepressants can be linked to aberrant neuroreceptor binding.
Objective:
This study aims to assess the antidepressant binding in brain regions of depressed nonresponders compared with healthy controls.
Materials And Methods:
Healthy volunteers and depressed subjects who had failed to benefit from at least 2 antidepressant treatments were recruited by newspaper advertisements. All subjects had received no antidepressant medication for at least 2 months before positron emission tomography (PET) that was carried out with [11C]mirtazapine. Kinetic parameters of [11C]mirtazapine were determined from PET data in selected brain regions by the simplified reference tissue model.
Results:
Binding potentials of [11C]mirtazapine in cerebral cortical regions were lower in depressed nonresponders than in healthy controls. Removal rates of [11C]mirtazapine were higher in diencephalic regions of depressed nonresponders than in healthy controls.
Conclusions:
PET neuroimaging with [11C]mirtazapine showed aberrant neuroreceptor binding in brain regions of depressed subjects who had failed to benefit from treatment with antidepressant drugs.
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