Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects

This multicenter study will enroll 300 members of familial Frontotemporal Dementia (FTD)
families across 8 experienced FTD research centers with a known mutation in MAPT, PGRN, or
C9ORF72 (100 mutation carriers with mild dementia or minimally symptomatic yet non-demented,
100 asymptomatic mutation carriers, and 100 clinically normal relatives who are non-mutation
carriers) to obtain annual assessments including T1-MRI, FLAIR, diffusion tensor imaging
(DTI), ASL perfusion (ASLp), intrinsic connectivity functional MRI (icfMRI), MR spectroscopy
(MRS), CSF, blood, and behavioral, neuropsychological and functional assessment, for a total
of three assessments per participant.

A primary goal of this study is to identify the most robust and reliable methods to track
disease progression in familial FTD so that disease-modifying therapeutic trials can be
designed appropriately.

Inclusion Criteria:

1. Must be a member of family with a known mutation in one of the three major FTLD
related genes: MAPT, PGRN, or C9ORF72.

2. At least 18 years of age.

3. The predominant phenotype in the kindred must be cognitive/behavioral (ie, kindreds in
whom parkinsonism or ALS is the predominant clinical phenotype among affected
relatives may be excluded)

4. Have a reliable informant who personally speaks with or sees that subject at least
weekly.

5. Subject is sufficiently fluent in English to complete all measures

6. Subject must be willing and able to consent to the protocol and undergo yearly
evaluations over 3 years.

7. Subject must be willing and able to undergo neuropsychological testing (at least at
baseline visit).

8. Subject must have no contraindication to MRI imaging.

Exclusion Criteria

1. Known presence of a structural brain lesion (e.g. tumor, cortical infarct).

2. Presence of another neurologic disorder which could impact findings (eg, multiple
sclerosis).

3. Subject is unwilling to return for follow-up yearly, undergo neuropsychological
testing and MR imaging.

4. Subject has no reliable informant.