A pilot dose finding study of pioglitazone in autistic children

• Published in: Molecular autism 2018-11, Vol.9 (1), p.59-59, Article 59
• Main Authors: Capano, Lucia, Dupuis, Annie, Brian, Jessica, Mankad, Deepali, Genore, Lisa, Hastie Adams, Rianne, Smile, Sharon, Lui, Toni, Odrobina, Dina, Foster, Jane A, Anagnostou, Evdokia
• Format: Article
• Language: English
• Subjects: Autism; Autism spectrum disorder; Autistic children; Autistic Disorder - drug therapy; Behavior; Chemokines; Child; Clinical trial; Clinical trials; Cytokines; Diabetes; Dosage and administration; Drug therapy; Drugs; Efficacy; Female; Humans; Immune system; Inflammation; Male; Pervasive developmental disorders; Pharmacology, Experimental; Pilot Projects; Pioglitazone; Pioglitazone - administration & dosage; Pioglitazone - adverse effects; Pioglitazone - pharmacokinetics; Pioglitazone - therapeutic use; Proteins; Social research; Studies; Treatment; Tumor necrosis factor-TNF
• ISSN: 2040-2392; 2040-2392
• DOI: 10.1186/s13229-018-0241-5

Pioglitazone is a promising compound for treatment of core autism spectrum disorder (ASD) symptoms as it targets multiple relevant pathways, including immune system alterations. This pilot study aimed to elucidate the maximum tolerated dose, safety, preliminary evidence of efficacy, and appropriate outcome measures in autistic children ages 5-12 years old. We conducted a 16-week prospective cohort, single blind, single arm, 2-week placebo run-in, dose-finding study of pioglitazone. Twenty-five participants completed treatment. A modified dose finding method was used to determine safety and dose response among three dose levels: 0.25 mg/kg, 0.5 mg/kg, and 0.75 mg/kg once daily. there were no serious adverse events (SAEs) and as such the maximum tolerated dose within the range tested was 0.75 mg/Kg once daily. overall, pioglitazone was well tolerated. Two participants discontinued intervention due to perceived non-efficacy and one due to the inability to tolerate interim blood work. Three participants experienced mild neutropenia. statistically significant improvement was observed in social withdrawal, repetitive behaviors, and externalizing behaviors as measured by the Aberrant Behavior Checklist (ABC), Child Yale-Brown Obsessive Compulsive Scale (CY-BOCS), and Repetitive Behavior Scale-Revised (RBS-R). Forty-six percent of those enrolled were deemed to be global responders. Pioglitazone is well-tolerated and shows a potential signal in measures of social withdrawal, repetitive, and externalizing behaviors. Randomized controlled trials using the confirmed dose are warranted. ClinicalTrials.gov, NCT01205282. Registration date: September 20, 2010.