Clozapine is the sole AP agent with superiority in treatment refractory schizophrenia, but it also is associated with the greatest risk of weight gain and other metabolic abnormalities. Topiramate, an anticonvulsant agent, possesses a weight-reducing effect. Furthermore, some studies have suggested that Topiramate may be associated with improvements in psychopathology in treatment refractory schizophrenia. Here the investigators propose to determine the role of topiramate for augmentation purposes (psychopathology) and as an adjunctive pharmacological intervention for weight loss in overweight/obese individuals with Ultra-Treatment Resistant Schizophrenia or Schizoaffective disorder taking clozapine.
Schizophrenia is a chronic illness characterized by social and vocational disruptive functioning. While \>70% of individuals with first episode illness respond to antipsychotics (APs), there remains a subgroup left with persisting psychotic symptoms. For these individuals, clozapine (CLZ) is also the sole drug with treatment superiority, but also carries the greatest metabolic liability. Another complicating factor in those treated with CLZ is the observation that while effective in some, 40-70% of individuals fail to show significant improvement with CLZ, often leading to augmentation strategies. While controlled trials are, in general lacking, a number of agents have been suggested as useful. One such group of medications includes the anticonvulsants. Topiramate represents one of the newer anticonvulsant agents approved for the treatment of epilepsy and prophylaxis of migraines. Importantly, topiramate possesses a weight-reducing effect that has been substantiated by a meta-analysis in non-psychiatric patients. Interestingly, topiramate has been studied as an adjunctive therapy in treatment-resistant schizophrenia with some evidence demonstrating small to moderate benefits with topiramate augmentation on psychopathology. However, these benefits must also be weighed against reports (primarily from epilepsy populations), that topiramate may cause cognitive dysfunction. This study will examine: 1. Topiramate-related effects on weight 2. Topiramate-related effects on glucose tolerance and insulin sensitivity 3. Topiramate-related effects on psychopathology and cognition 4. Topiramate-related effects on adiposity
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
50
Topiramate capsules starting with 25 mg b.i.d with an incremental increase of 25 mg b.i.d weekly upto a maximum of 100 mg b.i.d.
Placebo capsules visually identical to those containing topiramate will be administered.
Center for Addiction and Mental Health
Toronto, Ontario, Canada
RECRUITINGWeight loss
Measured in pounds
Time frame: 16 weeks
Insulin sensitivity
Measured through Oral Glucose Tolerance Test (pmol/L)
Time frame: 16 weeks
Psychopathology - Positive and Negative Syndrome Scale (PANSS)
Anchored scale to rate positive and negative psychiatric symptoms
Time frame: 16 weeks
Glucose Tolerance
Measured through Oral Glucose Tolerance Test (mmol/L)
Time frame: 16 weeks
Psychopathology - Brief Psychiatric Rating Scale (BPRS)
Anchored rating scale for psychiatric symptoms
Time frame: 16 weeks
Psychopathology - Clinical Global Impression (CGI)
Anchored scale to rate global impression of patient
Time frame: 16 weeks
Psychopathology - Global Assessment of Functioning (GAF)
Anchored scale to rate global functioning of patient
Time frame: 16 weeks
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