Cargando…
Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial
Down syndrome (DS) is the most common genetic cause of intellectual disability. The N-methyl-D-aspartate (NMDA) receptor uncompetitive antagonist, memantine hydrochloride (memantine), has been shown to improve learning/memory and rescue one form of hippocampus synaptic plasticity dysfunction in the...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410988/ https://www.ncbi.nlm.nih.gov/pubmed/22806212 http://dx.doi.org/10.1038/tp.2012.66 |
_version_ | 1782239790664515584 |
---|---|
author | Boada, R Hutaff-Lee, C Schrader, A Weitzenkamp, D Benke, T A Goldson, E J Costa, A C S |
author_facet | Boada, R Hutaff-Lee, C Schrader, A Weitzenkamp, D Benke, T A Goldson, E J Costa, A C S |
author_sort | Boada, R |
collection | PubMed |
description | Down syndrome (DS) is the most common genetic cause of intellectual disability. The N-methyl-D-aspartate (NMDA) receptor uncompetitive antagonist, memantine hydrochloride (memantine), has been shown to improve learning/memory and rescue one form of hippocampus synaptic plasticity dysfunction in the best-studied mouse model of DS available, the Ts65Dn mouse. Given the status of memantine as a treatment for Alzheimer's disease (AD) approved by the Food and Drug Administration, the preclinical evidence of potential efficacy in Ts65Dn mice, and the favorable safety profile of memantine, we designed a study to investigate whether the findings in the mouse model could be translated to individuals with DS. In this pilot, proof-of-principle study we hypothesized that memantine therapy would improve test scores of young adults with DS on measures of episodic and spatial memory, which are generally considered to be hippocampus dependent. Accordingly, in this randomized, double-blind, placebo-controlled trial, we compared the effect of 16-week treatment with either memantine or placebo on cognitive and adaptive functions of 40 young adults with DS using a carefully selected set of neuropsychological outcome measures. Safety and tolerability were also monitored. Although no significant differences were observed between the memantine and placebo groups on the two primary outcome measures, we found a significant improvement in the memantine group in one of the secondary measures associated with the primary hypothesis. Only infrequent and mild adverse events were noted. |
format | Online Article Text |
id | pubmed-3410988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34109882012-08-03 Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial Boada, R Hutaff-Lee, C Schrader, A Weitzenkamp, D Benke, T A Goldson, E J Costa, A C S Transl Psychiatry Original Article Down syndrome (DS) is the most common genetic cause of intellectual disability. The N-methyl-D-aspartate (NMDA) receptor uncompetitive antagonist, memantine hydrochloride (memantine), has been shown to improve learning/memory and rescue one form of hippocampus synaptic plasticity dysfunction in the best-studied mouse model of DS available, the Ts65Dn mouse. Given the status of memantine as a treatment for Alzheimer's disease (AD) approved by the Food and Drug Administration, the preclinical evidence of potential efficacy in Ts65Dn mice, and the favorable safety profile of memantine, we designed a study to investigate whether the findings in the mouse model could be translated to individuals with DS. In this pilot, proof-of-principle study we hypothesized that memantine therapy would improve test scores of young adults with DS on measures of episodic and spatial memory, which are generally considered to be hippocampus dependent. Accordingly, in this randomized, double-blind, placebo-controlled trial, we compared the effect of 16-week treatment with either memantine or placebo on cognitive and adaptive functions of 40 young adults with DS using a carefully selected set of neuropsychological outcome measures. Safety and tolerability were also monitored. Although no significant differences were observed between the memantine and placebo groups on the two primary outcome measures, we found a significant improvement in the memantine group in one of the secondary measures associated with the primary hypothesis. Only infrequent and mild adverse events were noted. Nature Publishing Group 2012-07 2012-07-17 /pmc/articles/PMC3410988/ /pubmed/22806212 http://dx.doi.org/10.1038/tp.2012.66 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Boada, R Hutaff-Lee, C Schrader, A Weitzenkamp, D Benke, T A Goldson, E J Costa, A C S Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title | Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title_full | Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title_fullStr | Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title_full_unstemmed | Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title_short | Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial |
title_sort | antagonism of nmda receptors as a potential treatment for down syndrome: a pilot randomized controlled trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410988/ https://www.ncbi.nlm.nih.gov/pubmed/22806212 http://dx.doi.org/10.1038/tp.2012.66 |
work_keys_str_mv | AT boadar antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT hutaffleec antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT schradera antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT weitzenkampd antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT benketa antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT goldsonej antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial AT costaacs antagonismofnmdareceptorsasapotentialtreatmentfordownsyndromeapilotrandomizedcontrolledtrial |