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Trends in Psychiatry and Psychotherapy

Print version ISSN 2237-6089On-line version ISSN 2238-0019

Trends Psychiatry Psychother. vol.38 no.2 Porto Alegre Apr./June 2016

http://dx.doi.org/10.1590/2237-6089-2015-0068 

Letter to the Editor

Effects of augmentation agents in autistic disorder patients treated with risperidone: a systematic review and a meta-analysis

Efeito de estratégias de potencialização da risperidona em pacientes com transtorno do espectro autista: revisão sistemática e metanálise

Amanda Soares1 

Pedro Shiozawa1 

Alisson Paulino Trevizol1 

Cristiane Silvestre de Paula2 

Rosane Lowenthal1 

Quirino Cordeiro1 

1 Laboratório de Neuromodulação Clínica, Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, SP, Brazil

2 Universidade Mackenzie, São Paulo, SP, Brazil


Different studies highlight the importance of augmentative strategies to risperidone as an effective pharmacological approach for treating behavioral symptoms associated with autistic spectrum disorder (ASD).1 The objective of the present study was to assess the combined clinical effects of different add-on pharmacological therapies to risperidone in the management of patients with ASD.

After searching MEDLINE and EMBASE databases, we performed a systematic review following the PRISMA statement guidelines.2 We also looked for controlled trials by contacting experts and searching the website clinicaltrials.gov. The criteria used to select articles were: 1) English language; 2) randomized, controlled trials; 3) mean and standard deviation values provided; and 4) response and remission rates provided. We excluded controlled trials assessing therapies different from our study objective. We opted to use Hedges' g to measure the effect size as it is appropriate for small sample sizes. The pooled effect size was weighted by the inverse variance method and measured under the random effect model. Heterogeneity was assessed using I2 index. We further used funnel plots to check for the existence of publication bias.

A total of 6 out of 51 randomized controlled trials met the eligibility criteria (n = 231, mean age = 8.25 years)3-9 (Table 1). In each trial reporting autistic symptoms, patients were clinically assessed by the Aberrant Behavior Checklist - Community version (ABC-C).10 Association of drugs with risperidone included: amantadine, N-acetylcysteine, topiramate, pentoxifylline, riluzole, and celecoxib.

Table 1 Demographic characteristics and clinical protocols 

Author Year Placebo (n) Active (n) Mean age (y) Augmentation strategy Active dosage (mg/d) Risperidone dosage (mg/d)
Mohammadi et al.10 2013 20 20 8 Amantadine 100-150 1-2
Ghanizadeh et al.8 2013 17 14 9.5 NAC 0.76 0.92
Rezaei et al.4 2010 20 20 7.5 Topiramate 150 2.5
Akhondzadeh et al.3 2010 20 20 8 Pentoxifylline 500 2.5
Ghaleiha et al.7 2013 20 20 8.5 Riluzole 1.2 1.6
Asadabadi et al.5 2013 20 20 8 Celecoxib 300 3

NAC = N-acetylcysteine; y = years.

Considering continuous reductions of autistic symptoms based on ABC-C scores, we found a significant clinical difference between the active control group and the placebo group for the irritability domain (Hedge's g = 1.23; 95% confidence interval [95%CI] 0.825-1.641; p = 0.000) and lethargy domain (Hedge's g = 0.735; 95%CI -0.163-1.307; p = 0.02). No significant difference was found for hyperactivity (Hedge's g = 0.651; 95%CI -0.098-1.402; p = 0.08) or stereotypic movements (Hedge's g = 0.892; 95%CI -0.021-1.806; p = 0.056) (Figure 1).

Figure 1 Forest plot of effect sizes (Hedges' g) for active versus placebo group treatment: A) irritability; B) hyperactivity; C) stereotypic behavior; D) lethargy. 95%CI = 95% confidence interval; SMD = standardized mean difference. 

Statistical analysis underscored the heterogeneity among studies (I2: 50.4%). Meta-regression analysis for possible confounding factors - such as baseline severity scores, age, sample size, and augmentation strategy - revealed no significant correlation with effect size. All studies were within the limits of Begg & Mazumdar's rank correlation test. Moreover, no study individually influenced the pooled effect size as assessed by the "metainf" command in Stata. In other words, our results suggested no difference between augmentation strategies in the subgroup analysis.

We found augmentation strategies to risperidone to be effective for amelioration of both irritability and lethargy in autistic patients. However, some limitations of the study - such as small number of trials and high heterogeneity - are factors that compromise its external validity. Nevertheless, we believe that the results presented underscore the benefits of combined therapy in comparison to risperidone alone and may work as a hypothesis-driven scenario for further clinical trials. The effectiveness of augmentation treatments to risperidone and the appropriate robustness of the strategy for treating autism are still unclear.

Augmentation strategies are promising tools for ameliorating both irritability and lethargy in patients with ASD. Further trials with larger samples will help to clarify the precise effects of augmentation strategies for this population

References

1. Barnard L, Young AH, Pearson J, Geddes J, O'Brien G. A systematic review of the use of atypical antipsychotics in autism. J Psychopharmacol. 2002;16:93-101. [ Links ]

2. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6:e1000100. [ Links ]

3. Akhondzadeh S, Fallah J, Mohammadi MR, Imani R, Mohammadi M, Salehi B, et al. Double-blind placebo-controlled trial of pentoxifylline added to risperidone: effects on aberrant behavior in children with autism. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34:32-6. [ Links ]

4. Rezaei V, Mohammadi MR, Ghanizadeh A, Sahraian A, Tabrizi M, Rezazadeh SA, et al. Double-blind, placebo-controlled trial of risperidone plus topiramate in children with autistic disorder. Prog Neuropsychopharmacol Biol Psychiatry . 2010;34:1269-72. [ Links ]

5. Asadabadi M, Mohammadi MR, Ghanizadeh A, Modabbernia A, Ashrafi M, Hassanzadeh E, et al. Celecoxib as adjunctive treatment to risperidone in children with autistic disorder: a randomized, double-blind, placebo-controlled trial. Psychopharmacology (Berl). 2013;225:51-9. [ Links ]

6. Ghaleiha A, Ghyasvand M, Mohammadi MR, Farokhnia M, Yadegari N, Tabrizi M, et al. Galantamine efficacy and tolerability as an augmentative therapy in autistic children: a randomized, double-blind, placebo-controlled trial. J Psychopharmacol . 2013;28:677-85. [ Links ]

7. Ghaleiha A, Mohammadi E, Mohammadi MR, Farokhnia M, Modabbernia A, Yekehtaz H, et al. Riluzole as an adjunctive therapy to risperidone for the treatment of irritability in children with autistic disorder: a double-blind, placebo-controlled, randomized trial. Paediatr Drugs. 2013;15:505-14. [ Links ]

8. Ghanizadeh A, Moghimi-Sarani E. A randomized double blind placebo controlled clinical trial of N-Acetylcysteine added to risperidone for treating autistic disorders. BMC Psychiatry. 2013;13:196. [ Links ]

9. Mohammadi MR, Yadegari N, Hassanzadeh E, Farokhnia M, Yekehtaz H, Mirshafiee O, et al. Double-blind, placebo-controlled trial of risperidone plus amantadine in children with autism: a 10-week randomized study. Clin Neuropharmacol. 2013;36:179-84. [ Links ]

10. Aman MG, Singh NN, Stewart AW, Field CJ. The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. Am J Ment Defic. 1985;89:485-91. [ Links ]

Received: October 12, 2015; Accepted: December 15, 2015

Correspondence: Pedro Shiozawa Departamento de Psiquiatria, Faculdade de Ciências Médicas da Santa Casa de São Paulo Rua Major Maragliano, 241, Vila Mariana 04017-030 - São Paulo, SP - Brazil Tel.: +55 (11) 3466.2105 E-mail: pedroshiozawa@gmail.com

No conflicts of interest declared concerning the publication of this article

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