NIH-funded research R01 grant

How elevated FGF-21 affects muscle loss due to mitochondrial problems

Official title: Autocrine Action of Elevated FGF-21 Contributing to Skeletal Muscle Atrophy in Response to Mitochondrial Dysfunction

Funded at University of Alabama at Birmingham · NIH-11175267 · Data updated 2026-11-12

This study is looking at how a protein called FGF-21 might play a role in muscle loss, especially for people dealing with issues like spinal cord injuries or being inactive for a long time, and it hopes to find new ways to help keep muscles healthy.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Alabama at Birmingham
NIH-funded
Lab location1 site (Birmingham, United States)
Project startAugust 15, 2021
Project endApril 30, 2026
Funding year2025
Award (this year)$438,441
NIH project number5R01AG069906-05
Project IDNIH-11175267 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include adults experiencing muscle atrophy due to conditions like spinal cord injuries or prolonged inactivity.

Less likely to help

Patients with muscle atrophy not related to mitochondrial dysfunction or those with unrelated chronic conditions may not benefit from this research.

What this research studies

This research investigates the role of elevated levels of FGF-21, a protein produced by muscles, in contributing to muscle atrophy, particularly in conditions of mitochondrial dysfunction. The study aims to understand the mechanisms behind muscle loss that can occur due to factors like spinal cord injuries or prolonged bed rest. By examining how mitochondrial health impacts muscle function and the signaling pathways involved, the research seeks to identify potential new therapeutic targets for preventing muscle wasting. Patients may be involved in understanding how these biological processes affect their muscle health and overall well-being.

Why it matters

Potential benefit: If successful, this research could lead to new treatments that prevent or reverse muscle atrophy, improving quality of life for affected patients.

How similar studies have gone: Previous research has shown promising results in understanding the role of mitochondrial dysfunction in muscle atrophy, suggesting that this approach could yield valuable insights.

Where this research is happening

  • University of Alabama at Birmingham
    Birmingham, United States
    Active

Researchers

  • Principal investigator: Rowe, Glenn Cameron — University of Alabama at Birmingham
  • Study coordinator: Rowe, Glenn Cameron

Related research

Other NIH-funded projects on the same topics.

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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.