Skip to main content

Spectrum: Autism Research News

Clinical research: Arthritis drug improves autism treatment

by  /  26 September 2012
THIS ARTICLE IS MORE THAN FIVE YEARS OLD

This article is more than five years old. Autism research — and science in general — is constantly evolving, so older articles may contain information or theories that have been reevaluated since their original publication date.

Double duty: Genes linked to autism overlap with those involved in arthritis.

The anti-inflammatory drug celecoxib, sometimes marketed as Celebrex, improves the effectiveness of risperidone for treating irritability in people with autism, according to a study published 11 July in Psychopharmacology1.

Celecoxib has also been shown to alleviate symptoms of schizophrenia2 and severe depression3.In the new study, researchers tested a combination of celecoxib and risperidone for treating symptoms of autism.

The researchers treated 40 children who have autism with risperidone for ten weeks. Half of them also took celecoxib, and the other half took a placebo. The children had not taken any drugs for at least six months prior to the study, but had taken antipsychotics at some point in the past.

Based on scores on the Aberrant Behavior Checklist, a parent questionnaire, children who took both drugs showed less irritability — and 11 showed no irritability at all — after ten weeks than those who took risperidone alone. In contrast, 12 of the children who received placebo had less irritability than before and 4 showed no irritability at all.

Celecoxib also improves the effectiveness of risperidone in treating social withdrawal and repetitive behaviors, but not hyperactivity or inappropriate speech, the study found.

Half of the celecoxib group and nine of the children taking placebo reported side effects, but not severe enough to withdraw from the study.

References:

1: Asadabadi M. et al. Psychopharmacology (Berl) Epub ahead of print (2012) PubMed

2: Akhondzadeh S. et al. Schizophr. Res. 90, 179-185 (2007) PubMed

3: Akhondzadeh S. et. al. Depress. Anxiety 26, 607-611 (2009) PubMed