What is ADNI?

The major goals of the Alzheimer’s Disease Neuroimaging Initiative (ADNI) are to:

1) Develop improved methods, which will lead to uniform standards for acquiring longitudinal, multi-site MRI and PET data on patients with Alzheimer’s disease (AD), mild cognitive impairment (MCI), and elderly controls.

2) Acquire a generally accessible data repository, which describes longitudinal changes in brain structure and metabolism. In parallel, acquire clinical, cognitive and biomarker data for validation of imaging surrogates.

3) Determine those methods, which provide maximum power to determine treatment effects in trials involving these patient groups. A team of investigators with considerable experience in AD clinical trials, MRI, PET, biomarkers and informatics has been assembled.

How will the study run?

    The first six months of the project will be devoted to establishing uniform MRI and PET acquisition techniques at all of the 40-45 participating sites, followed by initiation of subject recruitment. Improved methods for MRI and PET quantification will be assessed and implemented if useful. All subjects will have clinical/cognitive assessments and 1.5 T structural MRI every 6 months for 2-3 years. Approximately 50% of subjects will also have FDGPET scans at the same time intervals and 25% of subjects (who do not also have PET) will have MRI at 3 Tesla. AD subjects (n=200) will be studied at 0, 6, 12, and 24 months. MCI subjects at high risk for conversion to AD (n= 400) will be studied at 0, 6,12, 18, 24, and 36 months. Age matched controls (n=200) will be studied at 0, 6, 12, 24 and 36 months.
    All MRI and PET scans will be rapidly assessed for quality by the MRI and PET components of the Neuroimaging Center so that subjects may be rescanned if necessary. All clinical data will be collected, monitored, and stored by the Clinical Center at the AD Cooperative Studies program at UCSD. U Penn will collect biomarker samples. All raw and processed image data will be archived at LONI. Pilot studies will evaluate different image processing methods to measure brain regions of interest. All data will be monitored and analyzed by project statisticians, and data base queries will be performed on request.
    All clinical, cognitive, imaging, and biomarker databases will be linked and all raw, processed, and statistically analyzed data will be fully and rapidly accessible to the public through the Internet. The results of this study will be extremely useful for design of future AD and MCI trials.  

Eligibility Requirements:

If you are 55 or older, with or without memory problems then you are eligible for this study.

Visit Frequency:

Each visit will take approximately 4 hours.

There will be 4 visits if you have been diagnosed with Alzheimer’s disease; 5 visits if you have no problems, and 6 visits if you have mild memory problems.

Compensation:

The costs you incur for time and expenses due to your participation in this study will be compensated. Contact your study site to determine the exact amount of this compensation. For more information please contact Melina Griss at mgriss@harthosp.org, or by phone (860-545-7783).