The Impact of Lorazepam on Cognition in APOE e4 Carriers
Primary Purpose
Alzheimer's Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
lorazepam
placebo
Sponsored by
About this trial
This is an interventional screening trial for Alzheimer's Disease focused on measuring apolipoprotein E e4, Alzheimer's disease, somnolence, Early detection
Eligibility Criteria
Inclusion Criteria:
- a score of at least 28 on the MMSE
- a score of less than 10 points on the HAM-D-17
- age 50-65
- genotype APOE e3/e4 or APOE e4 non-carriers
- cognitively normal
Exclusion Criteria:
- significant medical, psychiatric, or neurological illnesses
- use of benzodiazepines within the previous four weeks
- currently using sedating antihistamines
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
1
2
Arm Description
single 2 mg dose of lorazepam
single dose of placebo
Outcomes
Primary Outcome Measures
Groton Maze Learning Task
Secondary Outcome Measures
Auditory Verbal Learning Test
1-back test
Full Information
NCT ID
NCT00586430
First Posted
December 21, 2007
Last Updated
December 21, 2007
Sponsor
Mayo Clinic
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT00586430
Brief Title
The Impact of Lorazepam on Cognition in APOE e4 Carriers
Official Title
The Impact of Lorazepam on Cognition in APOE e4 Carriers
Study Type
Interventional
2. Study Status
Record Verification Date
December 2007
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
July 2007 (Actual)
Study Completion Date
July 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Mayo Clinic
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
We expect the results of this pilot study to justify a larger study that follows people to determine if certain tests of memory and attention, performed while sleepiness is induced by a single dose of lorazepam (a widely used anti-anxiety medication) could predict an individual's risk of developing AD. We plan to compare cognitively normal people who possess a common gene that increases risk for AD- the apolipoprotein E (APOE) e4 allele-to individuals without this gene. We hypothesize that a single 2 mg dose of lorazepam will cause more cognitive impairment in carriers of the APOE e4 allele than in noncarriers, and that the carriers will recover more slowly from these impairments than noncarriers.
Detailed Description
We aim to compare measures of memory and information processing speed at 2.5 hours and 5 hours after the administration of a 2 mg dose of lorazepam or placebo in cognitively normal, 50-65 year old APOE e4 carriers and noncarriers, and determine the differential impact of lorazepam on cognition at each time point. Twenty carriers and 20 noncarriers matched for age, sex, and education will be drawn from a database of persons who have already undergone genotyping for an ongoing study at the Mayo Clinic, excluding people with evidence of depression or cognitive impairment and other medical, neurological or psychiatric conditions. Using a double blind, crossover design, subjects will receive either placebo or a 2 mg dose of lorazepam after baseline testing. Equivalent tests will be repeated 2.5 and 5 hours post challenge. The data analysis will compare APOE e4 carriers to noncarriers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease
Keywords
apolipoprotein E e4, Alzheimer's disease, somnolence, Early detection
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
single 2 mg dose of lorazepam
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
single dose of placebo
Intervention Type
Drug
Intervention Name(s)
lorazepam
Other Intervention Name(s)
Ativan
Intervention Description
single 2 mg dose of lorazepam
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
single dose of placebo
Primary Outcome Measure Information:
Title
Groton Maze Learning Task
Time Frame
baseline, 2.5 hours and 5 hours
Secondary Outcome Measure Information:
Title
Auditory Verbal Learning Test
Time Frame
baseline, 2.5 hours and 5 hours
Title
1-back test
Time Frame
baseline, 2.5 hours and 5 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
a score of at least 28 on the MMSE
a score of less than 10 points on the HAM-D-17
age 50-65
genotype APOE e3/e4 or APOE e4 non-carriers
cognitively normal
Exclusion Criteria:
significant medical, psychiatric, or neurological illnesses
use of benzodiazepines within the previous four weeks
currently using sedating antihistamines
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cynthia M Stonnington, M.D.
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
19573495
Citation
Stonnington CM, Snyder PJ, Hentz JG, Reiman EM, Caselli RJ. Double-blind crossover study of the cognitive effects of lorazepam in healthy apolipoprotein E (APOE)-epsilon4 carriers. J Clin Psychiatry. 2009 Oct;70(10):1379-84. doi: 10.4088/JCP.08m04593. Epub 2009 Jun 30.
Results Reference
derived
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The Impact of Lorazepam on Cognition in APOE e4 Carriers
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