Early Onset Alzheimer's Disease Genomic Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Baylor Research Institute
- Enrollment
- 26
- Locations
- 1
- Primary Endpoint
- Biomarkers found in blood
Study Overview
Brief Summary
The purpose of this study is to collect samples from patients with Early-Onset Alzheimer's disease (AD) and their immediate family members for molecular analysis. Samples will be studied in order to understand how molecular changes in the body are related to the development of the disease. Researchers will study your DNA and RNA in order to help doctors diagnose, treat, and monitor people at risk of developing Early-Onset AD in the future.
Detailed Description
About 50 people will be asked to take part in this study at this location. This will include participants with early-onset AD and their parents and siblings. Participants will be asked to: Sign this consent form or have a Legally Authorized Representative sign and provide the participant' health history. The study staff will review the participant's medical history and test results to see if the participant can be part of this study, The study staff will need to know any over-the-counter or prescription drugs, vitamins, or herbs taken by the participant. The study staff will discuss what is required to be part of this study. Participants cannot take part in this study if they have: Family history of early or late-onset Alzheimer's disease, Uncontrolled concurrent illness including psychiatric illness or situations that would limit compliance with the study requirements or the ability to willingly give written or verbal consent. If the participant agrees to take part in this study, one 8mL blood sample (about 2 teaspoons) will be collected from them. If the participant is receiving a clinically indicated blood draw, the blood collections for this study will occur at the same time. Participants may be required to have a research-specific blood draw if they are not scheduled for a blood draw during a regularly scheduled visit.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 40 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Diagnosis of early-onset Alzheimer's disease based on the NIA-AA diagnostic criteria as determined by the clinician. (Those patients with severe dementia due to Alzheimer's disease or who have impaired decisional capacity, may participate only if their legally authorized representative gives their consent.)
- •Male and female patients ≥40 and ≤65 years of age.
- •Parents and siblings of the participant with Alzheimer's disease.
Exclusion Criteria
- •Family history of early or late-onset Alzheimer's disease.
- •Uncontrolled concurrent illness including psychiatric illness or situations that would limit compliance with the study requirements or the ability to willingly give written or verbal informed consent
Arms & Interventions
Negative Control
Family members of patients with Early-Onset Alzheimer's disease who have consented to the study.
Early-Onset Alzheimer's disease
Patients ages 45-60 with Early-Onset Alzheimer's disease
Intervention: Genetic Testing (Genetic)
Outcomes
Primary Outcomes
Biomarkers found in blood
Time Frame: 2 years
Blood will be taken so that tests can be run to locate a biomarker that will help to diagnose and treat early-onset Alzheimer's disease.
Secondary Outcomes
No secondary outcomes reported