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A double-blind placebo controlled trial of piracetam added to risperidone in patients with autistic disorder
Shahin Akhondzadeh1, Hamid Tajdar, Mohammad-Reza Mohammadi
1Psychiatric Research Center, Roozbeh Psychiatric Hospital, Tehran University of Medical Sciences, South Kargar Street, Tehran, 13337, Iran. s.akhond@neda.net
Insights
Piracetam, a glutamate receptor modulator, showed significant improvements in autistic disorder symptoms when combined with risperidone. This combination therapy offers potential synergistic effects for treating autism.
Area of Science:
- Neuroscience
- Psychiatry
- Pharmacology
Background:
- Autism is hypothesized to involve glutamate system dysregulation (hypoglutamatergic disorder).
- Piracetam modulates AMPA-sensitive glutamate receptors, suggesting potential therapeutic value in autism.
Purpose of the Study:
- To evaluate the efficacy of piracetam as an add-on therapy to risperidone in children with autism spectrum disorder.
- To assess the impact of piracetam on disruptive symptoms associated with autism.
Main Methods:
- A 10-week, double-blind, placebo-controlled study involving 40 children (3-11 years) diagnosed with autism.
- Participants received either piracetam + risperidone (Group A) or placebo + risperidone (Group B).
- Outcomes were measured using the Aberrant Behavior Checklist-Community (ABC-C) Rating Scale.
Main Results:
- Piracetam combined with risperidone led to significant improvements in ABC-C scores compared to placebo + risperidone.
- Group A showed a mean change of -11.90 +/- 3.79 in ABC-C scores, versus -5.15 +/- 3.04 in Group B.
- The difference between groups was statistically significant (F = 5.85, P = 0.02).
Conclusions:
- Combining piracetam with atypical antipsychotics like risperidone may yield synergistic effects in managing autism symptoms.
- Glutamate-modulating agents like piracetam show promise as adjunctive treatments for autism spectrum disorder.
Abstract:
It has been reported that autism is a hypoglutamatergic disorder. Therefore, it was of interest to assess the efficacy of piracetam, a positive modulator of AMPA-sensitive glutamate receptors in autistic disorder. About 40 children between the ages three and 11 years (inclusive) with a DSM IV clinical diagnosis of autism and who were outpatients from a specialty clinic for children were recruited. The children presented with a chief complaint of severely disruptive symptoms related to autistic disorder. Patients were randomly allocated to piracetam + risperidone (Group A) or placebo + risperidone (Group B) for a 10-week, double-blind, placebo-controlled study. The dose of risperidone was titrated up to 2 mg/day for children between 10 and 40 kg and 3 mg/day for children weighting above 40 kg. The dose of piracetam was titrated up to 800 mg/day. Patients were assessed at baseline and after 2, 4, 6, 8 and 10 weeks of starting medication. The measure of the outcome was the Aberrant Behavior Checklist-Community (ABC-C) Rating Scale (total score). The ABC-C Rating Scale scores improved with piracetam. The difference between the two protocols was significant as indicated by the effect of group, the between subjects factor (F = 5.85, d.f. = 1, P = 0.02). The changes at the endpoint compared with baseline were: -11.90 +/- 3.79 (mean +/- SD) and -5.15 +/- 3.04 for group A and B respectively. A significant difference was observed on the change in scores in the ABC-C Rating Scale in week 10 compared with baseline in the two groups (t = 6.017, d.f. = 38, P < 0.0001). The results suggest that a combination of atypical antipsychotic medications and a glutamate agent such as piracetam, might have increase synergistic effects in the treatment of autism.
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