D2 dopaminergic receptor blockers, used to treat schizophrenia, can lead to the onset of movement disorders. Drug-induced movement disorders encompass several syndromes. Parkinsonism, dystonia, dyskinesia and akathisia are the most prevalent. All of them lead to poor adherence to the treatment instituted, decrease in the quality of life, relapses and hospitalizations. The pathophysiology of drug-induced movement disorders is complex and poorly understood, but seems to be associated with oxidative stress, as a result of an increase in free radicals generated from dopamine metabolism. Treatment strategies following the onset of drug-induced movement disorders include neuroleptic discontinuation, use of atypical antipsychotics and anticholinergics. A pre-clinical study showed that the antioxidant properties of vitamins B6 and B12, alone or in combination, prevented the development of orofacial dyskinesia induced by haloperidol. This clinical trial aims to evaluate the effects of vitamins B6 and B12 on the treatment of patients diagnosed with schizophrenia, schizoaffective or bipolar disorder who present with tardive dyskinesia, dystonia and parkinsonism.
D2 dopaminergic receptor blockers, used to treat schizophrenia, can lead to the onset of drug-induced movement disorders, such as parkinsonism, dystonia, dyskinesia and akathisia. They seem to be associated with oxidative stress, as a result of an increase in free radicals generated from dopamine metabolism. A preclinical study showed that vitamin B6 (pyridoxine) and B12 (cobalamin), alone or in combination, prevented the development of orofacial dyskinesia induced by haloperidol in an animal model of schizophrenia. Specific Aim1: To conduct a prospective, randomized, double-blind, placebo-controlled trial to evaluate the efficacy of 12-week adjuvant treatment with 200mg of pyridoxine (B6) or 2mg of cobalamin (B12) to treat drug-induced movement disorders of patients with schizophrenia, schizoaffective or bipolar disorder. The investigators will randomly assign 45 patients into three groups: placebo, B6 or B12 and check whether administration of vitamin B6 (pyridoxine) or B12 (cobalamin) attenuates drug-induced movement disorders (IDDM) in patients with diagnosis of schizophrenia, schizoaffective or bipolar disorder. Specific Aim 2: To quantify changes in serum markers of inflammation and biomarkers of oxidative stress in response to adjunctive treatment with B6 or B12. The hypothesis is that changes in these biomarkers will mediate the clinical response to them. Research Plan: The investigators will carry out a proof of concept 12-week prospective, randomized, double-blind, controlled trial of vitamin B6 and B12, at doses of 200 mg/day and 2mg/day, respectively, or identical placebo tablets, added to ongoing antipsychotics in 45 stable patients (ages 18-60 years, 15 patients per group) with diagnosis of schizophrenia, schizoaffective or bipolar disorder. The study will be conducted at the Drug Research and Development Center (NPDM), at the Universidade Federal do Ceará, Fortaleza, Brazil. This center has a long history of performing placebocontrolled trials in clinical medicine (http://www.npdm.ufc.br/) and has the necessary infrastructure to successfully complete the proposed study protocol. All participants will give written informed consent prior to study enrollment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
45
Adjuvant daily treatment with 200mg of pyridoxine
Adjuvant daily treatment with 2mg of cobalamin
Adjuvant daily treatment with placebo
Núcleo de Pesquisa e Desenvolvimento de Medicamentos - UFC
Fortaleza, Ceará, Brazil
RECRUITINGChange in the Simpson-Angus Extrapyramidal Symptoms Scale (SAS) scores
10-item rating scale to assess extrapyramidal symptoms; each item is scored 0-4, yielding a total between 0 and 40.
Time frame: Baseline and 12 weeks
Change in the Barnes Akathisia Rating Scale (BAS, BARS) scores
Objective Akathisia, Subjective Awareness of Restlessness and Subjective Distress Related to Restlessness are rated on a 4-point scale from 0 - 3 and are summed yielding a total score ranging from 0 to 9. The Global Clinical Assessment of Akathisia uses a 5-point scale ranging from 0 - 4.
Time frame: Baseline and 12 weeks
Change in the Abnormal Involuntary Movement Scale (AIMS) scores
10-item rating scale to assess involuntary movements; items are rated on a five-point scale of severity from 0-4, yielding a total between 0 and 40.
Time frame: Baseline and 12 weeks
Change in the Brief Psychiatry Rating Scale (BPRS) scores
18-item rating scale to assess changes in psychopathology; each item is scored 0-6, yielding a total between 0 and 40.
Time frame: Baseline and 12 weeks
Change in Plasma Glutathione (GSH)
GSH in ng/mL
Time frame: Baseline and 12 weeks
Change in serum level of Nitrite
Nitrite in nanomole/mililiter
Time frame: Baseline and 12 weeks
Change in serum level of Thiobarbituric acid reactive substances (TBARS)
TBARS in mmol of malonaldehyde/mL
Time frame: Baseline and 12 weeks
Change in serum level of Interleukin 1 β (IL-1β)
IL-1β in pg/mL
Time frame: Baseline and 12 weeks
Change in serum level of Interleukin-4
IL-4 in pg/mL
Time frame: Baseline and 12 weeks
Change in serum level of Interferon gamma (IFNγ)
IFNγ in pg/mL
Time frame: Baseline and 12 weeks
Change in serum level of Tumor necrosis factor alpha (TNF-α)
TNF-α in pg/mL
Time frame: Baseline and 12 weeks
Change in Indoleamine 2,3-dioxygenase (IDO) enzymatic activity
IDO activity in U IDO mol\^-1/mg\^-1
Time frame: Baseline and 12 weeks
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