Investigating genetic factors that influence the risk of ALS

SARM1 functional polymorphisms and their contribution to ALS risk

NIH-funded research Washington University · NIH-10989918

This study is looking at how changes in a specific gene called SARM1 might affect the chances of developing ALS, helping us understand how it can either harm or protect nerve cells, which could lead to new ways to help people with this condition.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionWashington University NIH-funded
Lab location1 site (Saint Louis, United States)
Project IDNIH-10989918 on NIH RePORTER

What this research studies

This research explores how specific genetic variations in the SARM1 gene may contribute to the risk of developing amyotrophic lateral sclerosis (ALS). By examining the role of SARM1 in axon degeneration, the study aims to understand how certain mutations can either promote or protect against neurodegeneration. The researchers will analyze the mechanisms by which SARM1 influences axon survival and cell death, potentially identifying genetic markers that could inform patient risk profiles. This work may lead to new insights into ALS pathology and therapeutic targets.

Who could benefit from this research

Good fit: Ideal candidates for this research include individuals with a family history of ALS or those diagnosed with the condition who may have specific genetic variants.

Not a fit: Patients with ALS who do not have any genetic variations related to SARM1 may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to better understanding of ALS risk factors and the development of targeted therapies.

How similar studies have performed: Other research has shown promising results in understanding genetic contributions to neurodegenerative diseases, suggesting that this approach may yield valuable insights.

Where this research is happening

Saint Louis, 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 Amyotrophic Lateral Sclerosis Motor Neuron 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.