NIH-funded research NIH-funded research

Platelet and lung vessel cell metabolism in scleroderma-related pulmonary hypertension

Official title: A platelet-fibroblast axis connecting bioenergetics and metabolism in SSc-pulmonary arterial hypertension

Funded at University of Pittsburgh at Pittsburgh · NIH-11193267 · Data updated 2026-11-12

This project looks at whether energy changes in platelets signal lung vessel cells to change glutamine use and worsen pulmonary hypertension in people with systemic sclerosis.

More Hypertension research and trials

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionUniversity of Pittsburgh at Pittsburgh
NIH-funded
Lab location1 site (Pittsburgh, United States)
Project startSeptember 20, 2022
Project endAugust 31, 2027
Funding year2025
Award (this year)$234,488
NIH project number5P50AR080612-04
Project IDNIH-11193267 on NIH RePORTER

Who could benefit from this research

Could help

Adults with systemic sclerosis who also have pulmonary arterial hypertension and who can provide blood samples and attend clinical visits are the best candidates.

Less likely to help

People without systemic sclerosis or without pulmonary arterial hypertension, or those unable to provide blood samples or travel to the study site, are unlikely to benefit directly.

What this research studies

If you have systemic sclerosis and pulmonary arterial hypertension (SSc-PAH), this project studies blood platelets and lung vessel fibroblasts to understand how their energy use and glutamine metabolism might drive blood vessel stiffening. Researchers will compare platelet mitochondrial function from patients with different severities of vascular disease and test how patient platelets influence glutamine use and collagen production in pulmonary fibroblasts. They will also explore whether imaging or blood-based measures of fibroblast glutamine uptake can serve as new diagnostic tools. The team aims to connect lab findings with patient samples to guide future tests or treatments that target platelet–fibroblast communication in SSc-PAH.

Why it matters

Potential benefit: Could lead to blood tests or imaging methods that detect early metabolic changes and to new therapies that reduce vessel stiffness in SSc-PAH.

How similar studies have gone: Prior work linking YAP/TAZ and glutaminase to vascular stiffness provides supporting preclinical evidence, but applying this to platelet–fibroblast signaling and diagnostics in SSc-PAH is a novel direction.

Where this research is happening

  • University of Pittsburgh at Pittsburgh
    Pittsburgh, United States
    Active

Researchers

  • Principal investigator: Chan, Stephen Y — University of Pittsburgh at Pittsburgh
  • Study coordinator: Chan, Stephen Y

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.