A Randomized Placebo-Controlled Cross-Over Pilot Study of Riluzole for Drug-Refractory Irritability in Autism Spectrum Disorder.
Riluzole at 200 mg/day does not reduce irritability in teens and young adults with ASD.
01Research in Context
What this study did
Crossman et al. (2018) gave 14 teens and young adults with autism either riluzole or a sugar pill for five weeks. Then they switched the groups so every teen tried both pills.
The team watched for changes in irritability using the ABC-I scale. They kept the dose at 200 mg per day the whole time.
What they found
Riluzole did not beat the placebo. Irritability scores stayed the same in both parts of the cross-over.
The drug was safe—no one dropped out—but it simply did not help.
How this fits with other research
Eisenhower et al. (2006) saw big wins with low-dose risperidone in a similar cross-over design. Risperidone cut irritability by half in about half of clients. The different result shows that not all pills work the same way.
Calamari et al. (1987) tested fenfluramine and also got nothing, just like riluzole. Two null drug trials remind us that medicine for autism irritability is hit-or-miss.
Hattier et al. (2011) reviewed dozens of tiny drug studies and found most use different rulers to measure behavior. Crossman et al. (2018) used the same ABC-I scale as many others, so their null finding is easier to compare.
Why it matters
You now have solid evidence that riluzole 200 mg is not worth trying for drug-refractory irritability. Save client time, insurance money, and side-effect risk. When medicine fails, turn back to behavior plans or explore risperidone with medical colleagues instead.
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02At a glance
03Original abstract
Riluzole is a glutamatergic modulator of particular interest in autism spectrum disorder (ASD). In this 12-week randomized, double-blind, placebo-controlled, crossover pilot study we evaluated the safety and tolerability of 5-week of adjunctive riluzole treatment (vs. 5-week of placebo, with 2-week washout period) targeting ASD-associated drug-refractory irritability in eight individuals age 12-25 years. All participants tolerated riluzole 200 mg per day, however there were no statistically significant findings for the overall treatment effect, the treatment effect by week within period of the study, or a cross-over effect across the periods of the study on the Clinical Global Impression Improvement Scale or the Aberrant Behavior Checklist Irritability subscale. The results of this trial indicate that 5-week of riluzole treatment was well tolerated, but had no significant effect on the target symptoms. Trial Registration ClinicalTrials.gov Identifier NCT02081027, Registered 5 August 2013, First participant enrolled 19 September 2013.
Journal of autism and developmental disorders, 2018 · doi:10.1007/s10803-018-3562-5