New urine tests to assess kidney health in Fabry disease

Urine podocyte and podocyte GL3: novel screening tools for phenotype assessment and treatment efficacy in Fabry disease

NIH-funded research University of Washington · NIH-10644824

This study is working on a simple urine test to help people with Fabry disease check for kidney damage by looking at important kidney cells and a specific substance, so they can get better care and treatment sooner.

Quick facts

Grant typeR03 grant
Study typeNIH-funded research
Funding institutionUniversity of Washington NIH-funded
Lab location1 site (Seattle, United States)
Project IDNIH-10644824 on NIH RePORTER

What this research studies

This research focuses on developing non-invasive urine tests to detect kidney damage in patients with Fabry disease, a genetic disorder caused by a deficiency in the enzyme alpha-galactosidase A. The study aims to quantify podocytes, which are crucial for kidney function, and measure the accumulation of a specific substance called GL3 in these cells. By using advanced imaging techniques and a specially created cell line, researchers will establish protocols to improve diagnosis and treatment timing for affected individuals. The goal is to enhance patient care by providing better tools for monitoring kidney health.

Who could benefit from this research

Good fit: Ideal candidates for this research are individuals diagnosed with Fabry disease, particularly those experiencing kidney-related symptoms.

Not a fit: Patients without Fabry disease or those who do not have kidney complications may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to earlier and more accurate diagnosis and treatment of kidney complications in Fabry disease patients.

How similar studies have performed: Other research has shown promise in using similar non-invasive techniques for monitoring kidney health in various conditions, indicating potential success for this approach.

Where this research is happening

Seattle, United States

Researchers

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 below.
Conditions Anderson-Fabry DiseaseFabry Disease
Last reviewed 2026-06-13 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.