A pilot dose finding study of pioglitazone in autistic children
Autor: | Jane A. Foster, Lisa Genore, Rianne Hastie Adams, Toni Lui, Annie Dupuis, Jessica Brian, Dina Odrobina, Sharon Smile, Evdokia Anagnostou, Deepali Mankad, Lucia Capano |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Male medicine.medical_specialty Efficacy Maximum tolerated dose (MTD) Pilot Projects Neutropenia Placebo lcsh:RC346-429 law.invention 03 medical and health sciences Physiological effects of drugs 0302 clinical medicine Developmental Neuroscience Randomized controlled trial law Internal medicine Medicine Humans Autistic Disorder Autism spectrum disorder Adverse effect Prospective cohort study Child Molecular Biology lcsh:Neurology. Diseases of the nervous system Inflammation Pioglitazone business.industry Research medicine.disease 3. Good health Clinical trial Treatment Psychiatry and Mental health 030104 developmental biology Safety profile Cytokines Female Drug therapy business 030217 neurology & neurosurgery Developmental Biology medicine.drug |
Zdroj: | Molecular Autism, Vol 9, Iss 1, Pp 1-14 (2018) Molecular Autism |
ISSN: | 2040-2392 |
Popis: | Background Pioglitazone is a promising compound for treatment of core autism spectrum disorder (ASD) symptoms as it targets multiple relevant pathways, including immune system alterations. Objective 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. Methods 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. Results Maximum tolerated dose: 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. Safety: 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. Early evidence of efficacy: 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. Conclusions and relevance 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. Trial registration ClinicalTrials.gov, NCT01205282. Registration date: September 20, 2010. Electronic supplementary material The online version of this article (10.1186/s13229-018-0241-5) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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