A Long Term Study Of Molecular And Structural Imaging In Atypical Alzheimer's Disease

Overview

About this study

The purpose of this study is to learn more about amyloid and tau burden in the brain of patients with Atypical Alzheimer's Disease and how that burden may change over a two-year period.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Over the age of 21

  • Must have an informant who will be able to provide independent evaluation of functioning

  • English is primary language

  • All subjects must have insidious onset, report progression of their symptoms, and meet current clinical diagnostic criteria for Logopenic variant Primary Progressive Aphasia or Posterior Cortical Atrophy

  • All subjects with LPA must present with early and dominant impairments in language

Exclusion Criteria:

  • A stroke or tumor that could explain symptoms

  • Subjects that present with early episodic memory impairment or meet clinical criteria for mild cognitive impairment

  • Meet specific criteria for another neurodegenerative disorder, including behavioral variant frontotemporal dementia, semantic dementia, primary progressive apraxia of speech, probable corticobasal syndrome, or progressive supranuclear palsy

  • Have poor vision (20/400)

  • Women that are pregnant or post-partum and breast-feeding

  • Are unable to undergo the tau-PET scan due to a prolonged QT interval on ECG

  • Have any of the following genetic conditions which can increase the chance of cancer: Cowden disease, Lynch syndrome, hypogammaglobulinemia, Wiskott-Aldrich syndrome, and Down's syndrome

  • MRI is contraindicated (metal in head, cardiac pace maker, etc.), have severe claustrophobia, or there are conditions that may confound brain imaging studies (e.g. structural abnormalities, including subdural hematoma or intracranial neoplasm)

  • Are medically unstable or are on medications that might affect brain structure or metabolism,(e.g. chemotherapy)

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jennifer Whitwell, Ph.D.

Open for enrollment

Contact information:

Sarah Boland

(507)284-3863

Boland.Sarah@mayo.edu

More information

Publications

Publications are currently not available
.
CLS-20200918

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