This study aims to examine both the genetic profile and the biomarkers implicated in keloid scar formation. Hypothesis: 1. Differences in the genetic profiles of lesional and non-lesional skin contribute a given population's propensity to develop keloids 2. Differences in biomolecules expressed in subjects with and without keloids can help predict keloid occurrence and severity 3. Biomarker analysis will provide useful insights for future targeted therapies for keloid scars
Objectives: 1. Determine gene expression profiles of keloid scar tissue using samples collected longitudinally 2. Define and compare the molecular biomarkers of keloid scars in keloid (lesional) and non-lesional skin biopsies and serum samples from adult subjects
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
48
Subjects will have their blood drawn during the first study visit. Subsequently, a punch biopsy and/or triamcinolone injection will be given based on group timeline.
Complete excision of an earlobe keloid will be taken.
Northwestern University Feinberg School of Medicine Department of Dermatology
Chicago, Illinois, United States
Keloid progression
Assess effectiveness of triamcinolone injection (keloid size measured in millimeters)
Time frame: One year
Gene Expression
Blood will be drawn during first study visit for analysis
Time frame: One year
Keloid recurrence
Assess keloid recurrence at biopsy site (measured by number of keloids)
Time frame: One year
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