ADNI Samples

ADNI is a complex and unique collection of clinical data, imaging, and biospecimens gathered longitudinally from carefully phenotyped participants. We recommend you learn details about participant characteristics and associated samples by familiarizing yourself with our dataset and previously approved RARC studies before submitting a sample request application.

Biospecimens collected from ADNI participants are managed by our Resource Allocation and Review Committees (RARCs). Requests for ADNI samples are reviewed (by the corresponding RARC) and ultimately approved or denied by NIA.

Biofluid RARC

Biofluid RARC
 

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Blood, plasma, serum, cerebrospinal fluid (CSF), and urine are managed by the Biofluid RARC.

Historical Availability of Biofluid Data
View the list of Previously Approved RARC Studies
About Biofluid Data

remote longitudinal monitoring cohort

Biospecimen Review
Committee (BRC)

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Genetic material is managed by the Biospecimen Review Committee (BRC). 

About Genetics & Related -Omics Data

remote digital cohort

Neuropathology RARC
(NP RARC)

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Brain tissues are managed by the Neuropathology RARC (NP RARC). Types of brain tissue available includes unstained slides, formalin-fixed wet tissue, and frozen.

Brain Tissue Regions Sampled for the ADNI
About Neuropathology Data

Apply for Access to Samples

Submit Initial Request Statement

Agree to Biosample policies and become familiar with the ADNI sample repository

Become familiar with the ADNI sample repository
The first step is to familiarize yourself with the ADNI sample repository to see if your request is appropriate for ADNI. See the links in the side bar.

Complete and submit Initial Request Statement

Parties interested in ADNI samples must submit an Initial Request Statement to catherine.conti@ucsf.edu and follow the appropriate template:

ADNI Biospecimens Initial Request Statement - Biofluids or Brain Tissues
ADNI Biospecimens Initial Request Statement - Genetics

Separate request statements must be submitted for Biofluids, Genetics, or Brain Tissue.

Initial Request Statement Review

The National Institute on Aging (NIA) will review based on the following evaluation criteria:

  • Appropriateness: ADNI samples are not for use in technology development.
  • Significance for advancing our understanding of AD and related dementias.
  • Scientific quality of the proposal.
  • Duplication of existing or approved studies and data already available from ADNI.
  • Commitment to data sharing as specified by ADNI. [Data Use Agreement]
  • Ability for investigator(s) to carry out the proposed work.
  • Impact on ADNI inventory of samples.

The NIA reviews Initial Request Statements and aims to provide a response within approximately one week. Approved requestors will be invited to submit the appropriate ADNI Full Application. 

Invitation to Submit Full Application

Submit the Appropriate Full Application

To make the most of the rich and complex ADNI data and biosamples available, please review the documents on the right before submitting a Full Application.
Depending on the sample type in your approved Initial Request Statement, please provide all information requested in the appropriate ADNI Biospecimens Full Application:

Sample Type Resource Allocation
Review Committee
Full Application
Biofluid: Blood,
plasma, serum, urine, CSF
Biofluid RARC Biofluid RARC Full Application
Genetic material Biospecimen Review
Committee (BRC)
at NCRAD
BRC Full Application
Brain tissue Neuropathology Core
(NPC) RARC
NPC RARC Full Application

Full Application submission timing

All RARCs will use the calendar below for their review cycles.

Date
Submitted
Approximate
Date of
Review
7/1 -8/3110/1
9/1-10/3112/1
11/1-12/312/1
1/1-2/284/1
3/1-4/306/1
5/1- 6/308/1

Full Application Review & Decision

Full Application Review & Decision

Applications will be reviewed by the appropriate RARC, which will provide its recommendation to the National Institute on Aging (NIA). The RARC reviews applications based on several criteria: 

  • Appropriateness: ADNI samples are not to be used for technology development
  • Significance for advancing our understanding of AD and related dementias.
  • Scientific quality of the proposal.
  • Duplication of existing studies and data already available from ADNI
  • Commitment to data sharing as specified by ADNI [Data Use Agreement]
  • Ability for investigator(s) to carry out the proposed work.
  • Impact on ADNI inventory of samples.

Applicant receives a decision

Within 2-3 weeks of the review, the NIA will notify the applicant of the review decision via email. The NIA may provide reviewer comments to the investigator, but will not provide a summary statement. Resubmissions will not be considered unless invited by the RARC or approved by the NIA. There is no appeal process. 

Complexity of ADNI Samples and RARCs
Biosample Policies

Full Application submission timing

All RARCs will use the calendar below for their review cycles.

Date
Submitted
Approximate
Date of
Review
7/1 -8/3110/1
9/1-10/3112/1
11/1-12/312/1
1/1-2/284/1
3/1-4/306/1
5/1- 6/308/1

Samples Released & Quarterly Updates

Samples distribution is discussed and samples shipped

The NIA will notify the ADNI Biomarker/Genetics/Neuropathology Core when a RARC Full Application is approved. The Core will work with approved investigators to finalize details about sample transfer. See Biosample Policies on RARC for MTA information. See NCRAD Pricing Schedule for costs of genetic sample distribution. While we do not charge for samples, there are associated costs for aliquoting, shipping, etc. which the investigator must cover. Samples will be shipped to the receiving investigator in a blinded fashion. The samples will be unblinded after the investigator submits study results back to the Core. Unblinded results are released to all ADNI data users on LONI, there is no embargo of results.

Biosample Policies on RARC
NCRAD Pricing Structure

Applicant must report a quarterly update on study progress

Each quarter that passes after an investigator has received samples, the requesting investigator must send a quarterly update on their study’s progress to catherine.conti@ucsf.edu.

In their Full Application, the investigator provides a timeline for expected results to come back to ADNI. If the originally proposed timeline is expected to be delayed more than a few weeks, the investigator must notify ADNI immediately. However, we strongly recommend that all investigators keep within their proposed timeline.

If an investigator’s ability to provide the data is substantially delayed, ADNI reserves the right to request that the samples be returned ASAP.

Applicant must report residual samples and additional studies

The investigator should notify NIA if there are residual samples left after completion of the RARC-approved study. Investigators are required to receive NIA approval (and RARC concurrence) before using residual samples in a new study. Investigators should not dispose of unused ADNI biofluid. Investigators may return residual samples to the Biomarker Core, where they will be pooled and used for assay standardization. Residual brain tissue is not to be used for additional unapproved studies. 

Submit Results to LONI

Applicant return results
After analysis is completed, investigator submits the following to the appropriate Core:

  • Methods Document
  • Data File (.csv)
  • Data Dictionary
  • IDA Data Submission Form
The approved investigator will be provided the Methods Document template and Data Submission Form. This will be reviewed by the Core and LONI for formatting and completeness and uploading onto the IDA.

Applicant cites ADNI in publications
Review and follow instructions for appropriate citation of ADNI in any publications resulting from ADNI sample and data use.

LONI provides code to unblind samples
Upon review of the returned data by the Core and LONI, LONI will provide a code that matches the unique ID of the specimens which can then be unblinded. The NIA is now allowing investigators with RARC approved ADNI biosample research applications to request a data embargo period of up to 2 months. This will give the investigator a 2-month period of access to the unblinded data before it is released to all ADNI users via LONI.

2024 Alzheimer’s Disease Neuroimaging Initiative
This website is funded by the Alzheimer’s Disease Neuroimaging Initiative