NIH-funded research R01 grant

Understanding how genetics influence the risk of chronic lung diseases like COPD and pulmonary fibrosis.

Official title: Uncovering the genetically-driven differential susceptibility to chronic obstructive pulmonary disease and pulmonary fibrosis

Funded at Brigham and Women's Hospital · NIH-11001125 · Data updated 2026-11-12

This study is looking at how our genes might affect the risk of developing lung diseases like COPD and IPF, and it aims to find out how these genetic differences can help us create more personalized treatments for patients.

More Fibrosis research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBrigham and Women's Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startDecember 15, 2022
Project endNovember 30, 2027
Funding year2025
Award (this year)$697,156
NIH project number5R01HL162813-03
Project IDNIH-11001125 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include individuals diagnosed with chronic obstructive pulmonary disease or idiopathic pulmonary fibrosis, particularly those with a family history of these conditions.

Less likely to help

Patients with other unrelated respiratory conditions or those without a genetic predisposition to COPD or IPF may not benefit from this research.

What this research studies

This research investigates the genetic factors that contribute to the differing risks of chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), two serious lung conditions. By analyzing genetic variants identified in previous studies, the researchers aim to uncover how these variants function as 'molecular switches' that influence disease development. The study will utilize advanced techniques, including CRISPR technology, to explore the underlying mechanisms and identify the specific lung cell types affected by these genetic factors. Patients may benefit from insights that could lead to more personalized treatment approaches based on their genetic profiles.

Why it matters

Potential benefit: If successful, this research could lead to improved understanding and treatment options for patients with COPD and pulmonary fibrosis.

How similar studies have gone: Previous genome-wide association studies have successfully identified genetic loci associated with COPD, suggesting that this approach has potential for uncovering new insights into disease mechanisms.

Where this research is happening

  • Brigham and Women's Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Cho, Michael H. — Brigham and Women's Hospital
  • Study coordinator: Cho, Michael H.

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.