Michelle Dawson posts

Post published on Twitter/X on 12 Dec 2012 01:55

Twitter/X Clinical trial clinicaltrials.gov DOI work crossref External link integrated into the post Autism terms

Structured cited links

2 cited resources

Clinical trial Fetched Post clinicaltrials.gov

University Hospital, Brest (2010). Efficiency of Bumetanide in Autistic Children. ClinicalTrials.gov. University Hospital, Brest.

Publication date
2010
Identifier
NCT01078714
Authors
University Hospital, Brest
Source
ClinicalTrials.gov
Reference type
clinical_trial
Publisher
University Hospital, Brest
Metadata source
clinicaltrials.gov

Abstract

The purpose of this study is to determine if a treatment by bumetanide presents an efficiency at the level of the neuronal maturation in the autism

DOI work Fetched Post crossref

E Lemonnier, C Degrez, M Phelep, R Tyzio, F Josse, M Grandgeorge, N Hadjikhani, Y Ben-Ari (2012). A randomised controlled trial of bumetanide in the treatment of autism in children. Translational Psychiatry, 2(12), e202-e202. Springer Science and Business Media LLC.

Publication date
11 Dec 2012
Identifier
10.1038/tp.2012.124
Authors
E Lemonnier, C Degrez, M Phelep, R Tyzio, F Josse, M Grandgeorge, N Hadjikhani, Y Ben-Ari
Source
Translational Psychiatry
Details
2(12), e202-e202
Reference type
article
Publisher
Springer Science and Business Media LLC
Metadata source
crossref

Abstract

Gamma aminobutyric acid (GABA)-mediated synapses and the oscillations they orchestrate are altered in autism. GABA-acting benzodiazepines exert in some patients with autism paradoxical effects, raising the possibility that like in epilepsies, GABA excites neurons because of elevated intracellular concentrations of chloride. Following a successful pilot study,(1) we have now performed a double-blind clinical trial using the diuretic, chloride-importer antagonist bumetanide that reduces intracellular chloride reinforcing GABAergic inhibition. Sixty children with autism or Asperger syndrome (3-11 years old) received for 3 months placebo or bumetanide (1 mg daily), followed by 1-month wash out. Determination of the severity of autism was made with video films at day 0 (D0) and D90 by blind, independent evaluators. Bumetanide reduced significantly the Childhood Autism Rating Scale (CARS) (D90-D0; P<0.004 treated vs placebo), Clinical Global Impressions (P<0.017 treated vs placebo) and Autism Diagnostic Observation Schedule values when the most severe cases (CARS values above the mean ± s.d.; n=9) were removed (Wilcoxon test: P-value=0.031; Student's t-test: P-value=0.017). Side effects were restricted to an occasional mild hypokalaemia (3.0-3.5 mM l(-1) K(+)) that was treated with supplemental potassium. In a companion study, chronic bumetanide treatment significantly improved accuracy in facial emotional labelling, and increased brain activation in areas involved in social and emotional perception (Hadjikhani et al., submitted). Therefore, bumetanide is a promising novel therapeutic agent to treat autism. Larger trials are warranted to better determine the population best suited for this treatment.

Study authors in this cited reference