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An Open-Label Trial of Donepezil in Fragile X Syndrome
This study is currently recruiting participants.
Verified by Stanford University, August 2007
First Received: September 15, 2005   Last Updated: February 22, 2008   History of Changes
Sponsored by: Stanford University
Information provided by: Stanford University
ClinicalTrials.gov Identifier: NCT00220584
  Purpose

Fragile X syndrome is the most common known inherited cause of neurodevelopmental disability. Functional magnetic resonance imaging (fMRI) studies from our laboratory indicate that specific brain regions using the neurochemical, acetylcholine, show significantly reduced activation during learning. Since donepezil is a medication that enhances acetylcholine function in the brain, the purpose of this study is to determine if donepezil has any beneficial effect on behavior or cognition in subjects with fragile X syndrome.


Condition Intervention Phase
Fragile X Syndrome
Drug: Donepezil
Phase I

Genetics Home Reference related topics: fragile X syndrome L1 syndrome
MedlinePlus related topics: Fragile X Syndrome
Drug Information available for: E 2020 Donepezil
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Dose Comparison, Single Group Assignment, Safety/Efficacy Study
Official Title: An Open-Label Trial of Donepezil in Fragile X Syndrome

Further study details as provided by Stanford University:

Primary Outcome Measures:
  • Scores on working memory tests at baseline, day 21, & day 42
  • Scores on learning tests at baseline, day 21, & day 42
  • Score on test of attention at baseline, day 21, & day 42
  • Scores on measures of behavior at baseline, day 21, & day 42

Estimated Enrollment: 10
Detailed Description:

Fragile X syndrome is the most common genetically inherited cause of neurodevelopmental disability in humans, affecting approximately 1:2000 to 4000 live births. Affected individuals have significant, long-term problems with learning, and often with behavior as well. The disorder is caused by the presence of a greatly expanded CGG repeat within the FMR1 gene on the long arm of the X chromosome. Abnormal methylation of this repeat, and adjacent areas within the FMR1 gene impedes transcription, ultimately resulting in reduced production of the FMR1 protein (FMRP). This protein is expressed in neurons, with particularly high levels of gene transcription occurring in the nucleus basalis (basal forebrain) and hippocampus. A recent functional imaging study from our group showed girls with fragile X to have greatly reduced levels of brain activation in the basal forebrain and hippocampal activation during a memory task. The nucleus basalis, is a cholinergic nucleus with widespread connections to the neocortex. It is critical to visuospatial attention in rodents and primates and is presumed to play a similar role in humans. The finding of decreased basal forebrain activation in girls with fragile X, considered in light of histological evidence showing high transcription levels of FMR1 in healthy nucleus basalis, suggests the possibility of a functional cholinergic deficit in fragile X syndrome.

Donepezil is an acetylcholinesterase inhibitor which slows the degradation of synaptic acetylcholine thereby increasing its availability. It is approved for the treatment of mild-moderate Alzheimer's disease. It has been studied in several other neurologic disorders--including vascular dementia, Lewy Body dementia, and Down's syndrome (with and without dementia)--where it has shown varying degrees of efficacy but consistently high degrees of safety and tolerability. The goal of the proposed study is to determine if enhancing cholinergic activity with donepezil has beneficial effects on behavior or cognition in subjects with fragile X syndrome.

  Eligibility

Ages Eligible for Study:   14 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:1. Confirmed genetic diagnosis of fragile X syndrome

2. Age e 14

3. Verbal IQ e 60 Exclusion Criteria:1. Currently taking any anticholinergic medications, tricyclic antidepressant medications, or diphenhydramine.

2. Presence of cardiac disease or bradycardia (< 60 beats/minute) at initial evaluation.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00220584

Locations
United States, California
Stanford University School of Medicine Recruiting
Stanford, California, United States, 94305
Contact: Amy A Lightbody, Ph.D.     650-724-2963     alightbody@stanford.edu    
Principal Investigator: Allan L Reiss            
Sponsors and Collaborators
Stanford University
  More Information

No publications provided

Study ID Numbers: 96239
Study First Received: September 15, 2005
Last Updated: February 22, 2008
ClinicalTrials.gov Identifier: NCT00220584     History of Changes
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Nootropic Agents
Neurotransmitter Agents
X-linked Mental Retardation and Macro-orchidism
Chromosome Disorders
Fragile X Syndrome
Cholinergic Agents
Mental Retardation
Cholinesterase Inhibitors
Heredodegenerative Disorders, Nervous System
Genetic Diseases, Inborn
Donepezil
Genetic Diseases, X-Linked
Neurologic Manifestations
Congenital Abnormalities
Neurobehavioral Manifestations

Additional relevant MeSH terms:
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Fragile X Syndrome
Cholinergic Agents
Heredodegenerative Disorders, Nervous System
Pathologic Processes
Therapeutic Uses
Syndrome
Donepezil
Genetic Diseases, X-Linked
Congenital Abnormalities
Neurobehavioral Manifestations
Nootropic Agents
Disease
Nervous System Diseases
Chromosome Disorders
Enzyme Inhibitors
Pharmacologic Actions
Mental Retardation
Cholinesterase Inhibitors
Genetic Diseases, Inborn
Sex Chromosome Disorders
Neurologic Manifestations
Mental Retardation, X-Linked
Central Nervous System Agents

ClinicalTrials.gov processed this record on May 06, 2009