Dominantly Inherited Alzheimer Network (DIAN)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWashington University School of Medicine

About this trial

The purpose of this study is to identify potential biomarkers that may predict the development of Alzheimer's disease in people who carry an Alzheimer's mutation.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Written informed consent obtained from participant and collateral source prior to any study-related procedures.

Aged 18 (inclusive) or older and the child of an affected individual (clinically or by testing) in a pedigree with a known mutation for ADAD.

Cognitively normal to very mild or mild cognitive impairment (CDR score range 0-1.0). Primary enrollment will focus on the recruitment of asymptomatic adult children who are more than 15 years younger than the estimated age of symptom onset. Enrollment of new participants with moderate cognitive impairment is allowed with the prior approval of the DIAN Coordinating Center.

Has two persons who are not their full-blooded siblings who can serve as collateral sources for the study.

Disqualifiers

Under age 18

Medical or psychiatric illness that would interfere in completing initial and follow-up visits

Requires nursing home level care

Has no one who can serve as a study informant

Trial population

Mutation carriers and non-carriers from families with a mutation (which is different from the genetic risk factor Apo-E4) known to cause Alzheimer's disease.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

700 Participants
are grouped into 2 trial groups
Group A: 1
Group B: 2

Trial outcomes

Primary outcomes

1

Positive predictive power of a biomarker or group of biomarkers

Time frame
Variable follow-up assessment based on age in relation to age at onset of affected parent.
2

Biomarkers obtained by blood draw, lumbar puncture, MRI, FDG PET, PET amyloid imaging

Time frame
Variable follow-up assessment based on age in relation to age at onset of affected parent
3

Clinical markers also examined from clinical interview and cognitive testing

Time frame
Variable follow-up assessment based on age in relation to age at onset of affected parent

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Washington University School of Medicine

Lead sponsor

National Institute on Aging (NIA)

Collaborator