This application from a new independent investigator seeks support for a study that addresses an important problem in geriatric psychopharmacology. Schizophrenia is a life-long illness requiring daily treatment with antipsychotic medication. In contrast to antipsychotic dosing in younger patients, the minimal therapeutic dose in older patients remains unknown. Clinical guidelines based primarily on expert consensus have recommended the use of lower antipsychotic doses in older patients with schizophrenia, and dose reduction has been advocated for patients stable on higher doses. However these guidelines are based on limited empirical data that do not take into account mechanistic processes involved in drug sensitivity associated with aging. Previous Positron Emission Tomography (PET) studies in young and mid-life patients with schizophrenia have established a therapeutic window of antipsychotic drug occupancy at striatal dopamine D2/3 receptors which has been successfully employed in predicting the clinically effective doses for new and established antipsychotic drugs in younger patients. Towards the goal of establishing the lowest effective maintenance dose of antipsychotic medication in older patients with early-onset schizophrenia, we propose a PET study using a prospective within-subject design. We will determine an estimate of risperidone D2/3 occupancy associated with maintenance of response in 40 patients 60 years and older with onset of schizophrenia before the age of 45 years and maintained on a single antipsychotic (risperidone) at a steady high dose of >3.5 mg per day for at least one year. They will undergo a gradual dose reduction up to 40% of their baseline dose to a target dose not lower than the recommended dose range of 1.25 - 3.5 mg/day. A [11C]raclopride PET scan will be completed at baseline and after dose reduction. They will then be followed for 6 months to determine clinical outcome. If they show signs of clinical deterioration, they will have their dose titrated up until clinical response is restored, and then undergo a third PET scan to establish the drug binding at the clinically effective dose. The results of this study will be used in future studies incorporating population pharmacokinetic methodology, translating the drug occupancy data collected in this to individualized dosing of risperidone for older patients with schizophrenia. This can be achieved in clinical practice using little more than standard laboratory assays to determine the lowest effective antipsychotic dose necessary for maintenance of therapeutic effect in older patients with schizophrenia, a clinical question of major public health significance.

Public Health Relevance

Schizophrenia is a life-long condition that requires long-term treatment with antipsychotic medications to prevent relapse of psychotic symptoms. As patients with schizophrenia become older, they become more sensitive to medication side effects and require a reduction of antipsychotic dose. However, since the minimal effective dose of antipsychotic medications in older patients is not known, most of them are treated with doses that are too high. Studying the extent of antipsychotic drug binding to brain receptors using positron emission tomography (PET) will allow for the prediction of the lowest effective dose required to maintain wellness in older patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH084886-01A2
Application #
7889483
Study Section
Interventions Committee for Adult Disorders (ITVA)
Program Officer
Evans, Jovier D
Project Start
2010-03-24
Project End
2015-01-31
Budget Start
2010-03-24
Budget End
2011-01-31
Support Year
1
Fiscal Year
2010
Total Cost
$159,352
Indirect Cost
Name
Centre for Addiction and Mental Health
Department
Type
DUNS #
207855271
City
Toronto
State
ON
Country
Canada
Zip Code
M5S2S-1
Caravaggio, Fernando; Fervaha, Gagan; Iwata, Yusuke et al. (2018) Amotivation is associated with smaller ventral striatum volumes in older patients with schizophrenia. Int J Geriatr Psychiatry 33:523-530
Caravaggio, Fernando; Iwata, Yusuke; Plitman, Eric et al. (2018) Reduced insulin sensitivity may be related to less striatal glutamate: An 1H-MRS study in healthy non-obese humans. Eur Neuropsychopharmacol 28:285-296
Caravaggio, Fernando; Scifo, Enzo; Sibille, Etienne L et al. (2018) Expression of dopamine D2 and D3 receptors in the human retina revealed by positron emission tomography and targeted mass spectrometry. Exp Eye Res 175:32-41
Gerretsen, Philip; Kim, Julia; Shah, Parita et al. (2018) BASIS: The blood pressure awareness and insight scale. J Clin Hypertens (Greenwich) 20:748-756
Gerretsen, Philip; Kim, Julia; Shah, Parita et al. (2018) OASIS: The Obesity Awareness and Insight Scale. Obes Med 9:38-44
Caravaggio, Fernando; Chung, Jun Ku; Gerretsen, Philip et al. (2017) Exploring the relationship between social attachment and dopamine D2/3 receptor availability in the brains of healthy humans using [11C]-(+)-PHNO. Soc Neurosci 12:163-173
Gerretsen, Philip; Pothier, David D; Falls, Carolyn et al. (2017) Vestibular stimulation improves insight into illness in schizophrenia spectrum disorders. Psychiatry Res 251:333-341
Rajji, Tarek K; Mulsant, Benoit H; Nakajima, Shinichiro et al. (2017) Cognition and Dopamine D2 Receptor Availability in the Striatum in Older Patients with Schizophrenia. Am J Geriatr Psychiatry 25:1-10
Chung, Jun Ku; Nakajima, Shinichiro; Plitman, Eric et al. (2016) ?-Amyloid Burden is Not Associated with Cognitive Impairment in Schizophrenia: A Systematic Review. Am J Geriatr Psychiatry 24:923-39
Fervaha, Gagan; Caravaggio, Fernando; Mamo, David C et al. (2016) Lack of association between dopaminergic antagonism and negative symptoms in schizophrenia: a positron emission tomography dopamine D2/3 receptor occupancy study. Psychopharmacology (Berl) 233:3803-3813

Showing the most recent 10 out of 34 publications