Tau Imaging in Young Onset Dementia
Status: | Completed |
---|---|
Conditions: | Alzheimer Disease, Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 45 - 70 |
Updated: | 2/21/2019 |
Start Date: | November 2014 |
End Date: | January 31, 2019 |
[18F]-T807 PET/CT Imaging of Tau Pathology in Young Onset Focal Dementia
The central goal of this study is to determine and compare the similarities and differences
in regional brain uptake of [18F]T807 in patients with typical Alzheimer's Disease (AD),
Posterior Cortical Atrophy (PCA), and Logopenic Variant of Primary Progressive Aphasia
(lvPPA). The investigators will correlate patterns of [18F]T807 binding with magnetic
resonance imaging (MRI)-based regional volumetric and cortical thickness measures. If
cerebral spinal fluid (CSF) samples are not available, patients may be asked to get an
optional lumbar puncture (LP) for additional comparisons. The investigators will recruit 20
participants, 45-70 years old, with clinical evidence of young onset focal dementia.
in regional brain uptake of [18F]T807 in patients with typical Alzheimer's Disease (AD),
Posterior Cortical Atrophy (PCA), and Logopenic Variant of Primary Progressive Aphasia
(lvPPA). The investigators will correlate patterns of [18F]T807 binding with magnetic
resonance imaging (MRI)-based regional volumetric and cortical thickness measures. If
cerebral spinal fluid (CSF) samples are not available, patients may be asked to get an
optional lumbar puncture (LP) for additional comparisons. The investigators will recruit 20
participants, 45-70 years old, with clinical evidence of young onset focal dementia.
Inclusion Criteria:
1. Participants will be 45 - 70 years of age
2. MMSE > 10 at screening visit.
3. Participants must be informed of the investigational nature of this study and provide
written informed consent in accordance with institutional and federal guidelines prior
to study-specific procedures. If the patient is unable to provide informed consent,
the patient's legal representative may consent on behalf of the patient but the
patient will be asked to confirm assent.
4. Participants must be willing and able to comply with scheduled visits and imaging
procedures.
5. A brain MRI is required. If a brain MRI has been performed within 6 months of
enrollment to this study and of adequate quality that scan may be used for the study
analysis, subjects who do not have a brain MRI will undergo a brain MRI either as a
part of this study
6. Participants must identify a study partner who is willing to accompany the patient to
study visits
Exclusion Criteria:
1. Females who are pregnant or breast feeding at the time of screening scan will not be
eligible for this study, urine or serum pregnancy test will be performed in women of
child-bearing potential at the time of screening
2. Inability to tolerate or contraindication to imaging procedures (PET/CT or MRI) in the
opinion of an investigator or treating physician
3. QTc > 450 msec on screening ECG.
4. Any medical or psychological conditions that, in the opinion of the investigator,
would compromise the subject's safety or successful participation in the study (e.g.
moderate to large stroke or history of moderate or severe traumatic brain injury
(TBI)).
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