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Clinical Trials/NCT00315575
NCT00315575
Completed
Not Applicable

BOLD and Perfusion fMRI of Alzheimer's Disease Risk

National Institute on Aging (NIA)1 site in 1 country90 target enrollmentAugust 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer's Disease
Sponsor
National Institute on Aging (NIA)
Enrollment
90
Locations
1
Primary Endpoint
identification of consistent patterns of variance in brain function in subjects at risk for Alzheimer's Disease by using APOE ε4 as a marker for disease risk
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to develop imaging techniques that can distinguish functional brain changes in people at high risk for dementia years prior to onset of clinical memory problems from those with normal changes of aging.

Detailed Description

The overall goals of this project are to identify consistent patterns of variance in brain function in patients at risk for Alzheimer's Disease by using APOE ε4 as a marker for disease risk. The activation Blood Oxygen Level Dependency (BOLD) signal will be compared to both resting and activation perfusion signals to assess the variability of cerebral blood flow as it relates to the BOLD signal. Each participant will be imaged on a 3T MRI scanner while performing an associate episodic memory task. A total of 90 individuals will be recruited for this study. Participants will be non-demented, right handed, adults with or without at least one APOE ε4 allele. Groups will be split as follows: A) ages 25-39: non-ε4 (n=15); B) ages 25-39: +ε4 (n=15); C) ages 40-49: non-ε4 (n=15); D) ages 40-49: +ε4 (n=15);.E) ages 50-65: non-ε4: F) ages 50-65: +ε4 (n=15). These groups will be matched for mean age, mean years of education, gender distribution, as well as the presence or absence of a family history of AD in a first degree relative. There will be 2 scanning sessions for each participant. Scan session #1 and Scan session #2 will be acquired within 2 weeks of each other and will take approximately one hour each.

Registry
clinicaltrials.gov
Start Date
August 2005
End Date
July 2008
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
National Institute on Aging (NIA)

Eligibility Criteria

Inclusion Criteria

  • Right-handed

Exclusion Criteria

  • Major medical illnesses
  • History of significant head trauma with residual cognitive deficits
  • Other neurological or major psychiatric disorders such as schizophrenia, bipolar disorder, developmental learning disorder, and alcohol or substance abuse
  • MRI contra-indications

Outcomes

Primary Outcomes

identification of consistent patterns of variance in brain function in subjects at risk for Alzheimer's Disease by using APOE ε4 as a marker for disease risk

Time Frame: single time point

Study Sites (1)

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