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Children with autism have a high rate of irritability and aggressive symptoms. Irritability or self-injurious behavior can result in significant harm to those affected, as well as to marked distress for their families. This paper provides a literature review regarding the efficacy and tolerability of pharmacotherapy for the treatment of irritability in autistic children. Although antipsychotics have not yet been approved for the treatment of autistic children by many countries, they are often used to reduce symptoms of behavioral problems, including irritability, aggression, hyperactivity, and panic. However, among antipsychotics, the Food and Drug Administration has approved only risperidone and aripiprazole to treat irritability in autism. Among atypical antipsychotics, olanzapine and quetiapine are limited in their use for autism spectrum disorders in children because of high incidences of weight gain and sedation. In comparison, aripiprazole and ziprasidone cause less weight gain and sedation. However, potential QTc interval prolongation with ziprasidone has been reported. Contrary to ziprasidone, no changes were evident in the QT interval in any of the trials for aripiprazole. However, head-to-head comparison studies are needed to support that aripiprazole may be a promising drug that can be used to treat irritability in autistic children. On the other hand, risperidone has the greatest amount of evidence supporting it, including randomized controlled trials; thus, its efficacy and tolerability has been established in comparison with other agents. Further studies with risperidone as a control drug are needed.
Treatment for autism spectrum disorders (ASDs) or pervasive developmental disorders (PDDs), which are a wide spectrum of disorders including autism and Asperger’s syndrome, includes therapeutic education regarding each symptom, arranging the environments of home or classroom, and pharmacotherapy. Pharmacotherapy is not curative, but rather serves as a treatment for secondary symptoms such as panic, hyperactivity, compulsion, and anxiety. Social impairment is best treated with behavioral therapy and social skills training.1 Stachnik et al.2 reported that among limited treatment options, non-pharmacologic approaches may be most beneficial, but in some cases presenting with behavioral abnormalities, pharmacotherapy may be needed. To the author’s knowledge, there has been little clear evidence assessing the adverse events of nonpharmacological interventions in ADSs,3,4 although one report indicated that there were no adverse events in social skills training5
Irritability may be defined as an individual being abnormally sensitive, with a disposition or tendency to easily exhibit uncontrolled anger or aggression.6 Children with autism and ASDs have a high rate of irritability and aggressive symptoms. In a study by Lecavalier,7 up to 30% of children with autism have symptoms of irritability, including aggression (24.5%), severe tantrums (30.2%), and deliberate self-injurious behavior (SIB) (16%). Horner et al.8 reported in their review that a high ratio of children with autism who were 8 years of age or younger were found to exhibit severe problem behaviors including tantrums (76%), aggression (61%), SIB (11%), and stereotypy (5%). However, the prevalence of these behaviors, specifically in autism, has not been as systematically evaluated.9,10 Irritability, aggression, and SIB can result in significant harm to those affected, and it can also lead to marked distress for the children’s families.11 In addition to its inherent potential dangerousness, irritability is frequently of sufficient severity to negatively impact the efficacy of educational and therapeutic interventions.12,13 The treatment of irritability in ASDs or PDDs is multimodal and includes the use of behavioral and pharmacologic approaches.6,13
This paper provides a literature review regarding the efficacy and tolerability of pharmacotherapy for the treatment of irritability in autistic children. Although a significant amount of literature regarding pharmacotherapy for the treatment of irritability in autistic children has been published, there are some disagreements among the previous reports concerning the efficacy and safety of these treatments. Furthermore, the approved use of antipsychotics or other categories of agents to these young patients is limited in many countries. However, if there is a history of behavioral symptoms that occur in multiple settings and that do not respond to behavioral interventions, pharmacotherapy is often required.14 This review focuses on the available evidence and clinical experience regarding pharmacotherapy for the treatment of irritability in autistic children. Medications used to treat the irritability will be discussed across categories of antipsychotics, antidepressants, a-2 adrenergic agonists, antiepileptic drugs, and others.
A literature review was conducted using the following PubMed search terms: “autistic spectrum disorder”; “pervasive developmental disorders”; and “autism” or “Asperger’s disorder.” The following limits were applied: randomized controlled trials (RCTs); “human trials”; and “English language.” Additional articles were identified from reference information. Studies were selected based on the following inclusion criteria: 1) a sample population that included children and adolescents; and 2) at least one standardized assessment of irritability or aggression as a primary outcome measure of the study. Trials involving hormones or drugs not approved by either Health Canada or the United States Food and Drug Administration (FDA) were excluded from the analysis.
We identified 23 RCTs that met the criteria. Of these, 15 RCTs were conducted with antipsychotic agents (two with aripiprazole, four with risperidone, one with olanzapine, two with clozapine, and five with haloperidol), and nine RCTs were conducted with miscellaneous agents that included antidepressants (one with clomipramine), a-2 adrenergic agonists (one with clonidine, one with guanfacine), antiepileptic drugs (one with lamotrigine, one with levetiracetam), drugs with central nervous system actions (two with methylphenidate, one with amantadine), and nutritional supplements (one with L-carnitine). Haloperidol was an active control in two RCTs.
The pharmacotherapy of irritability in autistic children primarily encompasses atypical antipsychotics, which are emerging as the first-line pharmacologic treatment for this target symptom.13 Although antipsychotics have not yet been approved for the treatment of autistic children by many countries, they are often used to reduce symptoms of behavioral problems including irritability, aggression, hyperactivity, panic, and SIB. However, among antipsychotics, the FDA has approved only risperidone and aripiprazole to treat irritability in autism.1,15 Thus, aripiprazole and risperidone will be mainly discussed in this review.
The atypical antipsychotics address both 5-hydroxytryptamine (5-HT) and dopamine (DA) function, and they may lead to fewer extrapyramidal symptoms (EPS), such as the antipsychotic-related dyskinesia, than typical antipsychotics. The 5-HT2 antagonism has been hypothesized to underlie the lower incidence rate of EPS; therefore, atypical antipsychotics have been considered better and safer treatment options than typical antipsychotics.16,17
Chavez et al.18 suggested that PDD is likely a heterogeneous disorder with a multifactorial etiology. The authors discussed the possible relationship between serotonin, DA, and norepinephrine and the observed clinical response to atypical antipsychotic treatment for autism, and they argued that the observed efficacy of atypical antipsychotics may be related to their ability to affect more than one neurotransmitter system.
The finding of hyperserotonemia19–21 in a significant percentage of individuals with autism suggests that serotonin may be a potential target for pharmacotherapy. DA neurotransmitter deregulation may also occur in autism. DA is associated with certain functions including attention, motivation, and planning. If these areas of cognition are impaired and certain behaviors occur, such as aggression or irritability, then treatment with antipsychotic agents may result in modest improvements.22
Aripiprazole is indicated in the US for the treatment of schizophrenia and bipolar I disorder, and it has been used as an adjunctive treatment of major depressive disorder; in addition, it has been recently approved to treat irritability associated with autistic disorder in children and adolescents 5–16 years of age.9,10 The efficacy and tolerability of aripiprazole, a dopamine D2 partial agonist23 that is distinctive from conventional antipsychotics, have been demonstrated in various psychiatric diseases. The mechanism of action underlying the effectiveness of aripiprazole in the treatment of ASDs has not been fully elucidated. A partial agonist effect on dopamine D224–26 and serotonin 5-HT1A27,28 receptors, and an antagonistic effect on serotonin 5-HT2A29 receptors, are proposed pharmacological activities that may be involved.
Aripiprazole has a time to maximum serum concentration (Tmax) of 2 hours in children and adolescents,30,31 and a long serum half-life (T1/2) of 75 hours in adults.32 Aripiprazole may be administered once daily, and its absorption does not appear to be affected by food. Steady-state concentrations are attained within 14 days of dosing. At steady-state, the pharmacokinetics of aripiprazole are dose-proportional. Elimination of aripiprazole is mainly through hepatic metabolism involving two P450 isozymes, CYP2D6 and CYP3A4, and aripiprazole may be subject to interactions with other drugs that are strong inhibitors or inducers of these enzymes. Aripiprazole does not have inhibitory or inducing effects on these or other CYP enzymes.31,32 The pharmacokinetic parameters in children and adolescents with autistic disorders are consistent with those seen in adults after adjusting for weight.32–34 The pharmacokinetic profile in a study conducted among children and adolescents with conduct disorder receiving 2–15 mg/day of aripiprazole for 14 days were linear, and the details for this study were as follows: mean maximum plasma concentration (Cmax), 21.8–194.2 ng/mL; median Tmax (time to Cmax), 2–4 hours; mean area under the plasma concentration time curve (AUC), 800–3879 ng*hour/mL; mean weight normalized apparent oral total body clearance (CLT/F), 0.03–0.07 L/hour/kg.35
The pharmacodynamic effects of risperidone are thought to be mediated via dopamine D2 and serotonin 5-HT2 A receptor antagonism.36–39 Risperidone and its active metabolite, 9-hydroxyrisperidone, have high in vitro binding affinity for these receptors, which results in significant inhibition of both serotonin and DA.36,37,39,40 The neurotransmitter binding profile of risperidone may provide the putative mechanisms for its antipsychotic effects, and it may lead to the generally lower incidence rate of adverse effects experienced relative to older antipsychotic agents.41
Risperidone is absorbed rapidly and has a high bio-availability (70%).37,38,42,43 The drug is 90% plasma protein bound and undergoes extensive hepatic metabolism, largely via cytochrome P450 (CYP) 2D6-mediated hydroxylation to 9-hydroxyrisperidone and, to a small extent, via N-dealkylation in adults.38,40 Risperidone and its metabolites are eliminated largely via the urine and partly via the feces in adults.38,40 In autistic children, peak plasma levels of risperidone and 9-hydroxyrisperidone were achieved ≈1 and 1–4 hours post-dose.37,38,42 The mean terminal half-lives of risperidone and 9-hydroxyrisperidone in autistic children were ≈2 and 11–16 hours, which were 30%–35% lower than those in adults.42
Olanzapine, a thienobenzodiazepine, exhibits a broad-based receptor profile including nanomolar binding affinity at several neurotransmitter binding sites.44 It further displays mesolimbic DA selectivity45 and a greater D4 than D2 receptor affinity.46 Olanzapine is uniquely associated with the release of both cortical DA and norepinephrine.47 As with clozapine, the 5-HT-related behavioral activity of olanzapine is several orders of magnitude greater than its DA-mediated effects.48 While not directly bound at the glutamatergic receptors, the preadministration of olanzapine antagonizes MK-801 and phencyclidine-induced behavioral disruptions mediated through the N-methyl-daspartate recognition site.49 Olanzapine also possesses a muscarinic cholinergic profile and demonstrates anticholinergic activity.48,50,51
Research into the pharmacotherapy of autism and related disorders began in the 1960s.13 Over time, as the typical antipsychotics (including chlorpromazine) were developed, investigators actively sought to determine their potential use in targeting the severe and often debilitating symptoms of aggression and SIB in autism.13 The attention of investigators was shifting away from the low-potency antipsychotics due to their propensity to induce sedation and result in cognition-related adverse effects. Researchers were increasingly drawn toward antipsychotics with potent D2 receptor antagonism, such as haloperidol, in their search for an effective treatment.13
Owen et al.10 conducted an 8-week, placebo-controlled, randomized, double-blind trial (number [N] = 98) to evaluate the efficacy of aripiprazole for treating irritability in patients aged 6–17 years with autistic disorder who had tantrums, aggression, SIB, or a combination of these symptoms. Ninety-eight patients were randomly assigned (1:1) to flexibly dosed aripiprazole (target dosage: 5 mg/day, 10 mg/day, or 15 mg/day) or placebo. The mean improvement in the Aberrant Behavior Checklist–Irritability (ABC-I) subscale score from week 1 through week 8 was significantly greater in the aripiprazole group than in the placebo group. Although the Clinical Global Impression–Improvement (CGI-I) score was also significantly improved, clinically significant residual symptoms may still persist for some patients. The EPS-related adverse event rate was 14.9% for aripiprazole and 8.0% for placebo; however, no serious adverse events were reported.10 These results suggested that aripiprazole was an effective treatment for irritability associated with autistic disorder, and the treatment was generally safe and well tolerated.
Marcus et al.9 conducted an 8-week, double-blind, randomized, placebo-controlled trial (N = 218) in children and adolescents aged 6–17 years with autistic disorder and who exhibited behaviors such as tantrums, aggression, and self-injury. Patients were randomly assigned to one of four groups (aripiprazole 5 mg/day, 10 mg/day, or 15 mg/day, and placebo). After 8 weeks, all aripiprazole dose groups exhibited significantly greater improvements in the caregiver-rated ABC-I score than did the placebo group. The clinician-rated CGI-I score was also significantly improved. The most common adverse event leading to discontinuation was sedation (23.6%). Two serious adverse reactions occurred: presyncope (5 mg/day) and aggression (10 mg/day).9 In this trial, aripiprazole was highly effective and well tolerated in children and adolescents with autistic disorder complicated by irritability.
Findling et al.52 conducted a multicenter, double-blind, randomized, placebo-controlled, relapse-prevention trial (N = 85) in the long-term maintenance treatment of pediatric patients (aged 6–17 years) with irritability associated with autistic disorder. In Phase 1, single-blind aripiprazole was flexibly dosed (2–15 mg/day) for 13–26 weeks. Patients with a stable response (≥25% decrease in the ABC-I subscale score and a rating of “much improved” or “very much improved” on the CGI-I) for 12 consecutive weeks were randomized into Phase 2 to continue aripiprazole or switch to placebo. In this study, the difference in time to relapse between aripiprazole and placebo was not statistically significant (P = 0.097); the Kaplan–Meier relapse rates at week 16 were 35% for aripiprazole and 52% for placebo (hazard ratio = 0.57; number needed to treat = 6). However, the authors concluded that both the hazard ratio and the number needed to treat suggest that some patients will benefit from maintenance treatment.52
In two 8-week, randomized, double-blind trials (n = 10153 and n = 5554) in autistic children and adolescents (aged 5–17 years), patients receiving oral risperidone (mean modal dosage of 1.37–1.96 mg/day) had significantly greater improvements from baseline in irritability scores than those receiving placebo. In modified intent-to-treat analyses, parent-rated ABC-I subscale scores were reduced by 56.9%53 and 65.0%54 from baseline in the risperidone groups versus a decrease of 14.1%53 and 34.7%,54 respectively, in the placebo groups. There were also significantly greater improvements from baseline for some of the other ABC subscale scores (stereotypic behavior, lethargy/social withdrawal, and/or hyperactivity/noncompliance) in the risperidone groups than in the placebo groups, and a significantly higher proportion of patients in the risperidone groups achieved a positive response.53,54
In the 8-week, randomized, double-blind, placebo-controlled trial, a risperidone/placebo solution (0.01–0.06 mg/kg/day) was administered to 79 children (aged 5–12 years) with PDD. Subjects taking risperidone (mean dosage: 0.04 mg/kg/day; 1.17 mg/day) experienced a significantly greater mean decrease on the irritability subscale of the ABC compared with those taking placebo. With respect to the study endpoint, risperidone-treated subjects exhibited a 64% improvement over baseline in the irritability score, which was almost double that noted among the placebo-treated subjects (31%). Risperidone-treated subjects also exhibited significantly greater decreases across the other four subscales of the ABC; on the conduct problem, insecure/anxious, hyperactive, and overly sensitive subscales of the Nisonger Child Behavior Rating Form (parent version); and on the Visual Analog Scale of the most troublesome symptom. More risperidone-treated subjects (87%) showed global improvement in their condition compared with the placebo group (40%). Somnolence, the most frequently reported adverse event, was noted in 72.5% (risperidone) versus 7.7% of subjects (placebo).55
The benefits of up to 6 months of risperidone treatment (mean dosage = 1.96 mg/day), in terms of the mean ABC-I subscale scores and clinician-rated CGI-I scores, were maintained in an open-label extension and double-blind, placebo-controlled, discontinuation trial (n = 63).56 Efficacy was also maintained in the longer term, according to secondary endpoints, including changes from baseline across most of the other mean ABC subscales,56 and in the parent-rated modified Ritvo–Freeman Real Life Rating Scale, the validated clinician-rated Children’s Yale–Brown Obsessive Compulsive Scale, and the clinician-rated Maladaptive Behavior Domain of the Vineland Adaptive Behavior Scales (MBD-VABS) scores.57
In a double-blind, placebo-controlled, pilot trial conducted among children (aged 6–11 years) with ASDs, it was found that at mean doses of 10 ± 2.04 mg/day of olanzapine was effective at globally improving autistic features based on the CGI-I (–2.25 on olanzapine versus –1.1 on placebo) and response rate (50% on olanzapine versus 20% on placebo). It was once again observed that olanzapine increased weight, appetite, and sedation.58
One team of researchers59–63 conducted several placebo and active controlled trials of haloperidol in children and adolescents with autism and associated irritability. While symptoms of irritability, maladaptive behavior, stereotypy, and withdrawal improved in many of the haloperidol trials, the side effect burden was high and included sedation, acute dystonia, and withdrawal dyskinesias.59–63 In an RCT of Remington et al.64 the authors compared clomipramine, haloperidol, and placebo in 36 patients with autism over the course of 7 weeks. Subjects ranged in age from 10–36 years (mean = 16.3 years) and 24 subjects were less than 18 years of age. Haloperidol was administered in a daily dose of 13 mg/day. Although no significant difference was found in the ABC-I subscale of aggression and SIB with haloperidol as compared to placebo, only haloperidol proved superior to baseline on a global measure of autistic symptom severity, as well as on specific measures for irritability and hyperactivity. Ten of the 33 subjects prematurely discontinued haloperidol treatment due to “behavioral problems” (n = 3), fatigue/lethargy (n = 5), depression (n = 1) and dystonia (n = 1).64
In an RCT by Remington et al.64 subjects were randomized to receive flexible doses of clomipramine 100–150 mg/day, haloperidol 1–1.5 mg/day, or placebo. In those patients who were able to complete a full therapeutic trial, clomipramine proved comparable to haloperidol in terms of improvement compared with baseline. However, significantly fewer individuals receiving clomipramine versus haloperidol were able to complete the trial (37.5% versus 69.7%) for reasons related to both side effects and efficacy or behavior problems.64
A trial by Fankhauser et al.65 used transdermal clonidine at doses of 0.16–0.48 mg/day in a 4-week double-blind, placebo-controlled, cross-over study of children and young adults aged 5–33 years. In the trial, the patch reduced symptoms including impulsivity, hyperarousal, and self-stimulating behavior.65
In a double-blind, placebo-controlled, crossover trial of eleven children aged 5–9 years with autism and/or intellectual disabilities for 6 weeks involving a maximum dose of 3 mg/day of guanfacine, Handen et al.66 noted benefits in hyperactivity and comorbid symptoms. About 45% of children had a 50% reduction in ABC hyperactivity. The CGI-I (P = 0.005), Parent ABC Hyperactivity subscale (P = 0.025), and Teacher ABC Hyperactivity subscale (P = 0.005) were found to have statistically significant differences between the guanfacine and placebo groups.66
In the blinded study conducted by Belsito et al.67 among 28 children (aged 3–11 years) with autism without epilepsy, the study showed no difference between lamotrigine and placebo on the ABC, the Autism Behavior Checklist, the VABS, the Pre-Linguistic Autism Diagnostic Observation Schedule, or the Childhood Autism Rating Scale (CARS) at a final dose of 5 mg/kg per day.67
In a double-blind, placebo-controlled trial of levetiracetam conducted with 20 children (aged 5–17 years) presenting with irritability and autism, Wasserman et al.68 compared an average dose of 862.5 mg to placebo. The authors reported no difference between the drug and placebo in terms of the patients’ mood and their scores on the irritability scales on the ABC, CY-BOCS, or Conners scales (long version for parent and teacher).68
Quintana et al.69 conducted a 4-week trial of ten patients with autistic disorder (aged 7–11 years). Patients were randomized to receive methylphenidate immediate-release (IR) 10 mg twice daily for 1 week, followed by methylphenidate IR 20 mg twice daily for 1 week, or placebo in a crossover design. At the endpoint, patients receiving methylphenidate had a statistically significant reduction in the Conners Teacher Questionnaire, the ABC-total, ABC-I, and ABC-hyperactivity scores (−0.5, −28.2, –7.8, and −13.4, respectively) compared to patients receiving placebo (−0.3, –17.8, −4.6, and −5.7, respectively). A statistically significant moderate reduction in hyperactivity symptoms was also observed.69 Handen et al.70 conducted the second RCT of methylphenidate in 13 children diagnosed with autism or PDD not otherwise specified with symptoms of attention-deficit hyperactivity disorder over 7 days using a double-blind, placebo-controlled, cross-over design. Subjects ranged in age from 5.6–11.2 years (mean = 7.4 years). Methylphenidate was administered in low (0.3 mg/kg) and high (0.6 mg/kg) doses two to three times daily. As compared to placebo, subjects who received methylphenidate showed significant improvements on the Hyperactivity Index of the Conners, IOWA Conners Teacher Rating Scale, and the Hyperactivity and Inappropriate Speech subscale on the ABC.70
In a double-blind, placebo controlled, 5-week trial by King et al.71 which was conducted among 39 children (aged 5–19 years) with autism, there were statistically significant improvements in the absolute changes in clinician-rated ABC–Community Version (ABC-CV) scores for hyperactivity (amantadine −6.4 versus placebo −2.1; P = 0.046) and inappropriate speech (−1.9 versus 0.4, respectively; P = 0.008) in the amantadine-treated group. Although the differences between groups were not statistically significant on the parent-rated ABC-CV, the active medication helped reduce symptoms of irritability and aggression in 47% of the children versus 37% of those on placebo. In terms of CGI-I score, 53% of those on amantadine improved versus 25% of those on placebo (P = 0.076).71
Geier et al.72 conducted a 3-month trial of 30 patients with ASDs (aged 3–10 years) who were randomized to receive either L-carnitine (50 mg/kg/day) or placebo. Patients who received L-carnitine had a statistically significant change in CARS score (–2.03) compared to patients who received placebo. A statistically significant reduction in the modified CGI-I score (–0.69) was observed with L-carnitine treatment compared to placebo, while a non-statistically significant reduction in the parent-rated Autism Treatment Evaluation Checklist total score was observed with L-carnitine compared to placebo.72
The reported clinical and safety outcomes of RCTs in children and adolescents with autism and irritability referenced above are summarized in Table 1.
In randomized, double-blind, placebo-controlled trials of autism in childhood and adolescence, the occurrence of EPS was more frequent in the aripiprazole group than in the placebo group, and salivation, tremor, and dystonia were observed.72,73 However, the degree of EPS was considered to be mild to moderate.72,73
No consensus has been reached regarding the occurrence rate of akathisia in patients taking aripiprazole. The occurrence rate of this side effect was comparable between the aripiprazole and placebo groups among those with autistic disorders.9,10 To the author’s knowledge, the prevalence of akathisia in autistic children receiving aripiprazole has not yet been clearly reported; however, akathisia occurred at a higher rate in child and adolescent patients receiving a higher dose of aripiprazole for the treatment of schizophrenia73 and bipolar I disorder.74
Serum prolactin was significantly reduced after aripiprazole administration compared with baseline, and it was also significantly lower in the aripiprazole group than in the placebo group in randomized, double-blind, placebo-controlled trials on autism.9,10
Contrary to ziprasidone,75–77 no changes were evident in blood pressure, heart rate, electrocardiography, or QT interval in any of the double-blind, placebo-controlled trials for aripiprazole conducted among children and adolescents with autistic disorder,9,10 or in those conducted with adolescents with schizophrenia.73
Weight gain, metabolic consequences. Aripiprazole causes less weight gain because it has a low affinity for histamine H1 receptors, and it is a partial agonist of serotonin 5-HT2C receptors, which are associated with weight gain and obesity.27,28,78 Additionally, because of the low affinity for the histamine H1 receptors, the incidence of oversedation is low.78 Furthermore, aripiprazole has almost no affinity for muscarinic M1 receptors, so it has few anticholinergic effects, such as constipation, dry mouth, urinary retention, or effects on cognitive function.79 In the nonrandomized Second-Generation Antipsychotic Treatment Indications, Effectiveness and Tolerability in Youth (SATIETY) cohort study, Correll et al.79 evaluated the effects of olanzapine, quetiapine, risperidone, and aripiprazole on body composition and metabolic parameters in 338 pediatric and adolescent patients who were treated for 12 weeks without prior antipsychotic medication exposure. The patients’ weight increased significantly in the antipsychotic treatment groups; aripiprazole caused the least amount of weight gain. Furthermore, serum total cholesterol, triglycerides, and nonhigh-density lipoprotein cholesterol (total cholesterol minus high-density lipoprotein cholesterol) increased significantly with olanzapine, quetiapine, and risperidone, but not with aripiprazole.79
On the other hand, in a long-term, placebo-controlled trial conducted with autistic children by Findling et al.52 aripiorazole patients gained an average of 1.6 kg of weight gain, which was more than the weight gained by placebo recipients. Therefore, careful monitoring of weight should be performed over the course of treatment with aripiprazole, although aripiprazole causes less weight gain in comparison with other atypical antipsychotics.
In a pooled descriptive analysis of short-term clinical trials,38 the most common treatment-emergent adverse events (ie, those occurring in >1.0% of patients receiving risperidone [n = 76] and at a rate that was at least twice that in the placebo group [n = 80]) were somnolence, increased appetite, fatigue, upper respiratory tract infection, increased saliva, constipation, dry mouth, tremor, and dystonia. The most common of these was somnolence, which was generally transient in nature.38
There was a higher incidence of adverse events associated with EPS in the risperidone group than in the placebo group in a pooled analysis of short-term trials evaluating risperidone treatment.38 In clinical trials, tardive dyskinesia occurred in two of 1,885 children and adolescents with autistic disorder or other psychiatric disorders receiving risperidone, with these cases resolving upon discontinuation of treatment.38
Eight children (28%) of 25 young autistic children (22 males and three females; age range, 3.9–7 years; mean age, 4.10 years) during treatment with risperidone (dosage range: 0.25–0.90 mg/day; mean dosage 0.52 mg/day) had prolactin levels (30 ng/mL) higher than two times the upper limit after 10 weeks of treatment.80 In double-blind trials, 49% of children and adolescents receiving risperidone had elevated serum prolactin levels, while 2% of patients did in the placebo group.38,81 Monitoring of prolactin during treatment with risperidone may be warranted.80
Weight gain and growth/sexual maturation. Risperidone treatment was associated with weight gain in short- and longer-term trials,53,56 with these increases being in excess of developmentally expected norms, and which follow a curvilinear trajectory and decelerate over time.82 There was no correlation between serum leptin levels and weight gain in 63 children and adolescents with autistic disorder receiving risperidone for up to 6 months. Serum leptin change does not reliably predict risperidone-associated weight gain.82
The long-term effects of risperidone on growth and sexual maturation remain to be fully evaluated.36,38 In a retrospective analysis of pooled data from five clinical trials conducted with 572 evaluable children (aged 5–15 years) with disruptive behavior disorders receiving risperidone for up to 1 year, there were no statistically significant or clinically relevant effects on growth, or on the onset or progression of puberty.38
Common adverse events included sedation and weight gain.6 Rhinitis, “glazed eyes,” constipation, and insomnia were also reported.58 Although olanzapine is a potentially effective treatment for irritability in autism because the risk of adverse events, including EPS, appears to be low, the increase in weight and appetite associated with olanzapine use may well be a limiting factor in its use and in its investigation for use in ASD.58,83–88
The most commonly reported adverse events were constipation, blunted affect, rigidity, dystonia, insomnia, increased appetite, depression, fatigue, and upper respiratory tract infection.6,89 A study by Perry et al.62 enrolled 60 children (age range, 2.3–7.9 years) with autism who were responders to haloperidol. The subjects were randomized to continuous or discontinuous (5 days on and 2 days off) treatment with haloperidol for 6 months, after which they all received 4 weeks of placebo. Although all were reversible, three youth developed dyskinesias during haloperidol treatment and nine developed withdrawal dyskinesias during the placebo period.62 Another study by Campbell et al.63 prospectively monitored the emergence of tardive dyskinesia and withdrawal dyskinesia in 118 children with autism aged 2.3–8.2 years. The youth received 6 months of haloperidol followed by 1 month of placebo, after which the need for another cycle of haloperidol treatment followed by placebo was assessed. In this study, 40 of 118 (33.9%) subjects developed dyskinesias, primarily reversible withdrawal dyskinesias. Of the individuals on a higher mean dosage (3.4 mg/day) of haloperidol during the study, nine of ten (90%) developed dyskinesias.63
In one study, the most notable side effects were insomnia and hyperactivity, at a final dose of 5 mg/kg per day. None of the children enrolled in the trial were withdrawn due to skin rash (a potentially serious adverse effect of lamotrigine treatment).67
In one RCT, adverse effects of decreased appetite, irritability, insomnia, stomachache, and headache were reported.69 In another RCT, five of 13 children experienced severe side effects, including social withdrawal, dullness, sadness, irritability, and skin picking. These side effects caused three subjects to be discontinued from the study.70
In the RCT, patients reported adverse effects of insomnia and somnolence more often.71
In the RCT, L-carnitine was generally well tolerated, with adverse effects of irritability and stomach discomfort.72
Greenaway and Elbe31 concluded in their review that in children and adolescents, aripiprazole appears to have minimal impact on the patients’ metabolic profile compared to most other atypical antipsychotics, and that aripiprazole may represent an important alternative for some children and adolescents who have experienced poor efficacy or significant metabolic adverse effects with their current antipsychotic treatment regimen.31 Their arguments are reconciled with other reports in that aripiprazole is generally safe and well tolerated in the treatment of irritability in autistic disorders.9,10,92–95 Aripiprazole also improves qualitative disorders in interpersonal interactions, including communication skills and motivation.94,95
In summary, compared with other antipsychotics, aripiprazole causes fewer adverse events that can lead to drug discontinuation (for example, EPS, weight gain, and sedation). Therefore, aripiprazole is associated with excellent treatment compliance and is a promising drug to improve treatment outcomes in ASDs.
Risperidone had a clinically manageable tolerability profile, with most adverse events being of mild to moderate intensity. There are some aspects of treatment, such as weight gain, somnolence, hyperprolactinemia, hyperglycemia, and EPS that require monitoring, and the long-term safety of risperidone in children with autistic disorder remains to be fully determined.36,37
Although olanzapine may be a promising treatment that is well tolerated for the treatment of some behavioral symptoms (irritability, hyperactivity/noncompliance, and lethargy/withdrawal) associated with ASDs, the risk of significant weight gain remains a concern.58,83–88 The non-RCT or short period trial limits the ability to make inferences about common side effects such as weight gain, lipidemia, and tardive dyskinesia. Further long-term RCTs of olanzapine are required.
The dearth of reports on the use of clozapine in ASDs is most likely due to its potential to cause life-threatening agranulocytosis, as well as its propensity to lower the seizure threshold. Frequent blood draws and cardiovascular monitoring, which are difficult procedures for children with autism, also make this atypical antipsychotic a less than ideal candidate.96 Patients with an impaired ability to communicate and those with cognitive impairments would likely encounter difficulty tolerating weekly to biweekly venipuncture to monitor white blood cell counts.97
Although potentially beneficial, the current role of haloperidol is limited to treatment-refractory patients due to concerns regarding its associated adverse effects, including frequently observed EPS.13
Due to the finding of increased insomnia and hyperactivity,67 lamotrigine is not a first-line agent to control irritable and aggressive symptoms in a population of children who frequently complain of insomnia and hyperactivity.96 The findings of increased aggression68,98 make levetiracetam a final option in the treatment of children with autism, unless the child has refractory epilepsy.96
In the RCT of King et al.71 clinician-rated improvements were noted in behavioral ratings following treatment with amantadine; however, parents did not report statistically significant behavioral changes with amantadine.
L-carnitine was proposed as a potential treatment for patients diagnosed with ASD to improve mitochondrial dysfunction. L-carnitine therapy administered for 3 months significantly improved several clinical measurements of ASD severity, but subsequent studies are recommended.72
In the RCT, clomipramine did not seem to be more effective, nor was it better tolerated in comparison with haloperidol or placebo.64
This study has some limitations. First, RCTs investigating the efficacy and tolerability of pharmacotherapy for the treatment of irritability in autistic children are still limited. Conclusions drawn from such studies must be evaluated with caution, and further accumulation of controlled studies is needed. Second, studies evaluating the long-term consequences of treatment are limited. Further investigations will provide the answers to these problems, which are fundamental for clinicians.
This paper reviewed the pharmacological profile and outcomes of previous clinical studies of pharmacotherapy for the treatment of irritability in autistic children. The four risperidone RCTs and the two aripiprazole RCTs reported statistically significant improvements in primary outcome measures. Thus, the bulk of positive RCT evidence regarding the pharmaco-therapy treatment of irritability in autism pertains to the FDA-approved antipsychotics risperidone and aripiprazole. RCTs supporting the efficacy of several alternative and adjunctive agents may afford additional treatment options when optimal antipsychotic doses fail to control symptoms or cause intolerable adverse effects.6
Among atypical antipsychotics, olanzapine58,85–87 and quetiapine99–101 are limited in their use for ASDs among children because of the drugs’ high incidences of weight gain and sedation. In comparison, aripiprazole79,102,103 and ziprasidone104,105 cause less weight gain and sedation, although there was no obvious trend in favor of aripiprazole regarding weight gain in a long-term observation study,52 and no RCTs have been conducted regarding the use of ziprasidone among autistic children. Furthermore, the potential QTc interval prolongation with ziprasidone has been reported.75–77 Contrary to ziprasidone, no changes were evident in the QT interval in any trials for aripiprazole.9,10,73 However, head-to-head comparison studies are needed to support the idea that aripiprazole may be a promising drug that can be used to treat irritability in autistic children. On the other hand, risperidone has the greatest amount of evidence to support it (including RCTs); thus, its efficacy and tolerability have been established in comparison with other agents. Further studies with risperidone as a control drug are thus needed.
ACADEMIC EDITOR: Praveen Kumar, Associate Editor
FUNDING: Author discloses no funding sources.
COMPETING INTERESTS: Author discloses no potential conflicts of interest.
This paper was subject to independent, expert peer review by a minimum of two blind peer reviewers. All editorial decisions were made by the independent academic editor. All authors have provided signed confirmation of their compliance with ethical and legal obligations including (but not limited to) use of any copyrighted material, compliance with ICMJE authorship and competing interests disclosure guidelines and, where applicable, compliance with legal and ethical guidelines on human and animal research participants. Provenance: the author was invited to submit this paper.
Conceived the concept: EK. Analyzed the data: EK. Wrote the first draft of the manuscript: EK. Made critical revisions: EK. The author reviewed and approved of the final manuscript.