Hidradenitis - an Analysis of Genetic Traits and Linkages in Families

Sponsor
University of Chicago (Other)
Overall Status
Recruiting
CT.gov ID
NCT05710393
Collaborator
(none)
500
1
86.5
5.8

Study Details

Study Description

Brief Summary

The aim of this study is to find a genetic link or family trait connecting persons with Hidradenitis Suppurativa (HS) to each other. As a result, discover the cause and perhaps treatment for Hidradenitis Suppurativa (HS).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Hidradenitis suppurativa (HS) is a chronic, debilitating skin disease characterized by multiple abscesses located predominantly in areas such as armpit, genital, pelvic, and perineum. It is considered an orphan disease of unknown origin and no existing treatment with a population prevalence estimated between 1-4%. It develops in otherwise healthy patients after puberty and affects patients life-long. HS often requires multiple surgical procedures to drain large abscesses, or hospitalization to treat infected wounds, can lead to feelings of personal embarrassment and social stigmatization.

    Anecdotal evidence from affected families shows that HS often "runs in families" and may be inherited in a Mendelian fashion; however, no adequately powered study has been undertaken to investigate this hypothesis. This project aims to characterize the inheritance pattern of HS in families, and identify the genetic cause of this disease in those families with evidence for monogenic inheritance.

    Data collection includes blood sample analysis (DNA), medical history, and information pertaining to any known family history of HS, from which a familial pedigree can be generated. This 'family-based' genetic study design will include both affected and unaffected family members, ideally spanning several generations. Therefore, study patients will be asked to refer their immediate and extended (affected and unaffected) family members to this research study.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Family-Based
    Time Perspective:
    Cross-Sectional
    Official Title:
    Hidradenitis Suppurativa - a Mendelian Trait? Genetic Pedigree and Linkage Analysis
    Actual Study Start Date :
    Sep 17, 2019
    Anticipated Primary Completion Date :
    Dec 1, 2025
    Anticipated Study Completion Date :
    Dec 1, 2026

    Arms and Interventions

    Arm Intervention/Treatment
    Affected

    (Affected) persons with a medical history of symptoms related to Hidradenitis Suppurativa.

    Unaffected-control

    (Unaffected) family of participants, having no history of symptoms related to Hidradenitis Suppurativa.

    Outcome Measures

    Primary Outcome Measures

    1. Hidradenitis Suppurativa Genetic linkage [1-Day Study Participation]

      Determine the genetic linkage of Hidradenitis Suppurativa (HS). Measurements are based on Gene panel assays of DNA specimen (blood or saliva) to find rare variant(s) linked to HS. Specimen samples include those provided by affected participants, and when possible they're biological family. A Gene panel diagnostic determines the number of variants (or mutation) in multiple genes, potentially identifying a genetic linkage of mendelian inheritance.

    Secondary Outcome Measures

    1. Demographics of Participant Population [1-Day Study Participation]

      Compare demographic variables of the affected population to analyze HS symptom history. Statistical Analysis of data collected via participant interview: Gender (at birth) Race (ethnicity) Age (at symptom start) Health history (related to HS) Family history (related to HS)

    2. Pattern of Affected Family [1-Day Study Participation]

      Measure inheritance proximity pattern of biologically related family, affected by HS symptoms. A 'Pedigree' will be generated using family history data collected during the study interview: Immediate family - parental, sibling, children Extended family (paternal vs maternal) - uncle, aunt, cousin Outcomes could span multiple generations.

    3. Number of Variants Shared [1-Day Study Participation]

      Determine the number of shared rare variants (or mutations) in genes associated with HS, between affected participants and their family. Measured by Gene panel assay of DNA specimen (blood or saliva) A Gene panel diagnostic determines the number of variants (or mutation) in multiple genes, potentially identifying a genetic linkage of mendelian inheritance.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    7 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Participants (affected) with Hidradenitis Suppurativa and related symptoms

    • Family (unaffected) of participants with Hidradenitis Suppurativa

    Exclusion Criteria:
    • Children under 7-years of age

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Chicago Medicine Chicago Illinois United States 60637

    Sponsors and Collaborators

    • University of Chicago

    Investigators

    • Principal Investigator: Peter Nagele, MD, MSc, University of Chicago Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Chicago
    ClinicalTrials.gov Identifier:
    NCT05710393
    Other Study ID Numbers:
    • IRB18-1861
    First Posted:
    Feb 2, 2023
    Last Update Posted:
    Feb 2, 2023
    Last Verified:
    Jan 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Chicago
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 2, 2023