NIH-funded research NIH-funded research

Understanding how heparan sulfate affects alpha-synuclein in Lewy body dementia

Official title: Heparan sulfate-mediated mechanisms of alpha-synuclein pathology in dementia with Lewy bodies disease

Funded at University of Alabama at Birmingham · NIH-11606576 · Data updated 2026-11-12

A small study in people who have dementia with Lewy bodies looks at how a brain sugar (heparan sulfate) helps a harmful protein (alpha-synuclein) spread, with the hope of slowing disease progression.

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionUniversity of Alabama at Birmingham
NIH-funded
Lab location1 site (Birmingham, United States)
Project startSeptember 1, 2026
Project endAugust 31, 2027
Funding year2026
Award (this year)$499,648
NIH project number1R56NS144587-01A1
Project IDNIH-11606576 on NIH RePORTER

Who could benefit from this research

Could help

Adults with or at risk for dementia with Lewy bodies who could participate in related biomarker or translational studies.

Less likely to help

The study may not benefit patients if the mechanisms do not translate to humans or if therapies are not effective.

What this research studies

This grant explores how alpha-synuclein builds up in the brain and how heparan sulfate on brain cells helps this process. Researchers have found that disrupting the interaction between α-syn fibrils and heparan sulfate can slow pathology in animal models, and they are testing strategies that could interfere with that interaction. The work focuses on aging brains and aims to identify approaches that could one day reduce neurodegeneration and improve function in patients with Lewy body–related dementia. The project combines molecular studies with experiments in models to translate findings toward human relevance. If successful, the approach could point to new therapeutic targets for dementia with Lewy bodies.

Why it matters

Potential benefit: It could lead to new ways to slow or halt progression of Lewy body dementia by targeting heparan sulfate interactions with alpha-synuclein.

How similar studies have gone: Prior work in animal and cell models showed that disrupting HS–α-syn interactions reduces pathology, supporting potential translational value.

Where this research is happening

  • University of Alabama at Birmingham
    Birmingham, United States
    Active

Researchers

  • Principal investigator: Aguilar Calvo, Patricia — University of Alabama at Birmingham
  • Study coordinator: Aguilar Calvo, Patricia

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.