NIH-funded research P01 program project

Imaging TDP-43 changes in primary progressive aphasia and genetic frontotemporal dementia

Official title: Biological Bases for Neuroimaging Signatures of TDP-43 in Primary Progressive Aphasia and Genetic FTLD

Funded at University of Pennsylvania · NIH-11265593 · Data updated 2026-11-12

This project aims to find brain imaging markers of the TDP-43 protein in people with primary progressive aphasia and inherited frontotemporal dementia so doctors can better tell these cases apart from tau-related disease.

Quick facts

Grant typeP01 program project
Study typeNIH-funded research
Funding institutionUniversity of Pennsylvania
NIH-funded
Lab location1 site (Philadelphia, United States)
Project startSeptember 15, 2020
Project endDecember 31, 2030
Funding year2026
Award (this year)$329,904
NIH project number2P01AG066597-06A1
Project IDNIH-11265593 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are people diagnosed with primary progressive aphasia (especially semantic-variant or non-fluent/agrammatic variants) or individuals with known genetic frontotemporal lobar degeneration who can travel to the study center.

Less likely to help

People whose language problems come from other causes (such as Alzheimer’s disease or stroke) or those unable to undergo imaging visits are unlikely to benefit directly from this project.

What this research studies

You would be part of research comparing brain scans and language tests from people with different types of primary progressive aphasia and those with genetic frontotemporal lobar degeneration. Researchers will look at patterns of gray-matter and white-matter degeneration and brain network connectivity that match TDP-43 versus tau pathology. They will use clinical language measurements, neuroimaging, and comparisons to genetic and autopsy data to link imaging patterns to the underlying proteinopathy. The goal is to create imaging signatures that indicate whether TDP-43 is driving the disease in a living person.

Why it matters

Potential benefit: If successful, this could let clinicians identify TDP-43 pathology in living patients using MRI or related brain imaging, improving diagnosis and tracking of disease.

How similar studies have gone: This approach is relatively novel—while imaging markers exist for tau pathology, there are currently no established in-vivo imaging biomarkers specific for TDP-43, so the work is largely untested.

Where this research is happening

  • University of Pennsylvania
    Philadelphia, United States
    Active

Researchers

  • Principal investigator: Gee, James C — University of Pennsylvania
  • Study coordinator: Gee, James C

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.