NIH-funded research R01 grant

Genetics of hidradenitis suppurativa in diverse populations

Official title: Whole genome sequencing analysis of hidradenitis suppurativa

Funded at Henry Ford Health + Michigan State University Health Sciences · NIH-11195106 · Data updated 2026-11-12

Researchers will use whole-genome sequencing to find genetic differences that might explain why hidradenitis suppurativa affects some people, especially African American and Hispanic/Latino patients, more severely.

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 year2025
Award (this year)$614,933
NIH project number5R01AR083553-02
Project IDNIH-11195106 on NIH RePORTER

Who could benefit from this research

Could help

People diagnosed with hidradenitis suppurativa who can provide a DNA sample or allow access to their genetic data, especially those of African American or Hispanic/Latino ancestry, are ideal candidates.

Less likely to help

People without HS or those seeking immediate changes to their medical care are unlikely to get direct clinical benefit from participating in this genetic research.

What this research studies

If you join this project, researchers will use whole-genome sequencing to scan all of your DNA for genetic changes linked to hidradenitis suppurativa (HS). They will compare genetic data from African American, Hispanic/Latino, and White patients and look for differences that might help explain racial and sex-related gaps in who gets HS and how severe it is. The team will combine new sequencing with existing resources such as the All of Us WGS data to increase the number of people studied and search for both rare and common variants. Results aim to point to biological pathways behind painful nodules, abscesses, and scarring and to guide future personalized approaches.

Why it matters

Potential benefit: If successful, this work could clarify genetic reasons for disparities in HS and eventually help guide more targeted prevention or treatment strategies.

How similar studies have gone: Only one prior genome-wide association study for HS has been published, so whole-genome sequencing in diverse groups is relatively novel though genetics has been implicated in HS risk.

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.