NIH-funded research R01 grant

Whole-genome sequencing to understand hidradenitis suppurativa in diverse groups

Official title: Whole genome sequencing analysis of hidradenitis suppurativa

Funded at Henry Ford Health + Michigan State University Health Sciences · NIH-11404883 · Data updated 2026-11-12

Researchers will study the genetic factors that contribute to hidradenitis suppurativa, especially in African American, Hispanic/Latino, and White patients, to better understand why some people are more affected.

More Hidradenitis Suppurativa research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionHenry Ford Health + Michigan State University Health Sciences
NIH-funded
Lab location1 site (East Lansing, United States)
Project startSeptember 18, 2024
Project endAugust 31, 2029
Funding year2026
Award (this year)$636,297
NIH project number5R01AR083553-03
Project IDNIH-11404883 on NIH RePORTER

Who could benefit from this research

Could help

People with hidradenitis suppurativa, especially from African American, Hispanic/Latino, and White populations, who consent to genomic research.

Less likely to help

Participants who decline genetic research or whose data do not reveal useful genetic associations may not receive direct benefit.

What this research studies

This project will analyze the entire genome of people with hidradenitis suppurativa to find genetic differences that might explain why the disease affects certain groups more than others. By combining newly generated data with existing genetic resources, the team aims to identify genetic risk factors that contribute to HS and its disparities. The work will involve sequencing DNA from diverse patient cohorts and comparing variants across groups to see which genetic differences associate with HS risk and severity. The goal is to build a clearer picture of HS biology that could guide future diagnostics and therapies. Participation would involve genetic analysis from consenting participants and access to existing data resources.

Why it matters

Potential benefit: If successful, the research could lead to better understanding of HS causes and ultimately more precise, personalized approaches to prevention and treatment.

How similar studies have gone: Past genetic studies of HS have been limited, with only one broad genetic association study published, making this work particularly novel and potentially impactful.

Where this research is happening

  • Henry Ford Health + Michigan State University Health Sciences
    East Lansing, United States
    Active

Researchers

  • Principal investigator: Mi, Qing-Sheng — Henry Ford Health + Michigan State University Health Sciences
  • Study coordinator: Mi, Qing-Sheng

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.