Study of Retinal Findings in People With Signs and Symptoms of Alzheimer s Disease Enrolled in 09-M-0198

Sponsor
National Eye Institute (NEI) (NIH)
Overall Status
Terminated
CT.gov ID
NCT02226835
Collaborator
(none)
33
1
29.4
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Study Details

Study Description

Brief Summary

Background:
  • Alzheimer s disease affects the brain and causes memory and thinking problems in older people. Macular degeneration (MD) is an eye condition. It is the leading reason that people over age 55 in the United States lose their central vision. Central vision is important for seeing fine details and for tasks like reading and driving. A feature of Alzheimer s disease is plaques in the brain. A feature of age-related MD is deposits in the retina in the eye. Researchers want to learn more about these diseases and find out if they are related.
Objective:
  • To see whether there is a relationship between Alzheimer s disease and age-related macular degeneration.
Eligibility:
  • People with or without Alzheimer s disease enrolled in another study. Participants must have someone to help them take part in this study.
Design:
  • Participants will be screened through the other study. They will have 1 visit. The tests will take about 3 hours.

  • Participants will answer questions about their medical and eye history.

  • Participants will have an eye exam to test how well they see. Their eye pressure will be measured and their eye movements will be checked.

  • Participants will get eye drops to dilate their pupils. Researchers will take pictures of the retina and the inside of the eye. Researchers may measure the thickness of the retina.

  • Participants will continue to receive care from their regular eye doctor during and after the study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Objective:

    Age-related macular degeneration (AMD) and Alzheimer s disease (AD) are both neurodegenerative diseases which affect a similar demographic of patients. Beyond age being a common risk factor for both diseases, an important common characteristic is a similarity in pathology findings, specifically, the presence of amyloid (beta) (A(beta)) in the senile plaques of the AD brain and in the drusen of AMD patients. As both of these diseases are the cause of significant morbidity of the quickly growing aging population, understanding the pathogenesis of both and identification of any overlapping pathophysiology will lead to a better understanding of each disease. The objective of this study is to investigate the presence of AMD and other neurodegenerative lesions and characterize retinal findings in a group of participants with well-phenotyped AD.

    Study Population:

    Up to 150 participants (100 symptomatic, 50 controls) will be recruited from patients already enrolled and participating in the National Institute of Mental Health (NIMH) study, 09-M-0198, Screening and Evaluation of Patients with Signs and Symptoms of Alzheimer s Disease.

    Design:

    This is a single center, cross-sectional, observational study that will include a single eye clinic visit with eye exam, visual acuity, photography and optical coherence tomography (OCT) testing.

    Outcome Measures:

    The primary outcome is the presence of AMD or other retinal findings in patients diagnosed with AD. Secondary outcomes will include autofluorescence imaging, spectral domain OCT and visual acuity.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    33 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    An Investigation of Retinal Findings in Patients With Signs and Symptoms of Alzheimer's Disease Enrolled in 09-M-0198
    Study Start Date :
    Aug 13, 2014
    Actual Primary Completion Date :
    Jan 24, 2017
    Actual Study Completion Date :
    Jan 24, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Photographs and images of subjects' eyes [Study completion]

    Secondary Outcome Measures

    1. OCT measurement [Study completion]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    • INCLUSION CRITERIA:

    • Patient must be enrolled in the 09-M-0198 protocol.

    • In those participants that require special assistance, we will request that they be accompanied by a care taker to provide proper care and monitoring.

    EXCLUSION CRITERIA:
    Patients:
    • The diagnosis of a different type of dementia, including frontotemporal dementia, normal pressure hydrocephalus, Lewy body dementia, Parkinson s disease dementia, Huntington s disease, or vascular dementia.

    • Any medical contraindication to the procedures performed in the study, or any current severe medical or psychiatric illness other than Alzheimer s disease.

    • Behavioral symptoms that would preclude the gathering of data for the study, or advanced disease such that participants cannot provide assent.

    Controls:
    • The diagnosis of a brain disorder.

    • Any medical contraindication to the procedures performed in the study, or any current severe medical or psychiatric illness.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Eye Institute (NEI)

    Investigators

    • Principal Investigator: Catherine A Cukras, M.D., National Eye Institute (NEI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    National Eye Institute (NEI)
    ClinicalTrials.gov Identifier:
    NCT02226835
    Other Study ID Numbers:
    • 140173
    • 14-EI-0173
    First Posted:
    Aug 27, 2014
    Last Update Posted:
    Sep 27, 2018
    Last Verified:
    Jan 24, 2017
    Keywords provided by National Eye Institute (NEI)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 27, 2018