NIH-funded research R01 grant

NGF Metabolic Dysfunction as a Marker of Cognitive Decline in Autosomal Dominant Alzheimer's Disease

Official title: Nerve Growth (NGF) Factor Metabolic Dysfunction as a Marker of Cognitive Decline in Autosomal Dominant Alzheimer's Disease

Funded at Boston University (Charles River Campus) · NIH-11591274 · Data updated 2026-11-12

This project looks at nerve growth factor pathways in people with a genetic form of Alzheimer's to see if blood and spinal fluid markers can identify early brain changes before symptoms appear.

More s Disease research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBoston University (Charles River Campus)
NIH-funded
Lab location1 site (Boston, United States)
Project startJuly 15, 2022
Project endJune 30, 2027
Funding year2026
Award (this year)$287,235
NIH project number7R01AG077627-03
Project IDNIH-11591274 on NIH RePORTER

Who could benefit from this research

Could help

Individuals who carry pathogenic PSEN1 mutations (autosomal dominant Alzheimer’s disease) and non-carrier family members.

Less likely to help

People without the genetic risk or with unrelated forms of dementia may not benefit from these biomarker findings.

What this research studies

Researchers will examine protein markers related to NGF metabolism in blood and CSF from people who carry pathogenic PSEN1 mutations (autosomal dominant AD) and from non-carriers, to see if these markers signal preclinical brain changes. The study focuses on a well-defined, early-disease population to reduce variability and better understand NGF-related biology in the progression to Alzheimer’s dementia. By comparing mutation carriers and non-carriers over time, the project aims to identify patterns that could support earlier detection and potential future interventions. The work uses biofluid samples from participants and analyzes them with biomarker assays to map NGF pathways across the disease course.

Why it matters

Potential benefit: If successful, the findings could enable earlier identification of people on the path to AD dementia and guide the timing of future therapies.

How similar studies have gone: Prior research has linked NGF metabolism changes to AD pathology, but this study focuses on a genetically defined population to clarify the biomarker signals.

Where this research is happening

  • Boston University (Charles River Campus)
    Boston, United States
    Active

Researchers

  • Principal investigator: Quiroz, Yakeel T. — Boston University (Charles River Campus)
  • Study coordinator: Quiroz, Yakeel T.

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.