Defining the Skin and Blood Biomarkers of Ichthyosis

Netherton Syndrome Clinical Trial

Official title:

Defining the Skin and Blood Biomarkers of Ichthyosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03417856
• Other study ID #: 2014-15801
• Status: Recruiting
• Start date: January 31, 2018
• Est. completion date: December 31, 2025

Study information

• Verified date: March 2024
• Source: Northwestern University
• Contact: Dermatology CTU
• Phone: 312-503-5944
• Email: NUderm-research[@]northwestern.edu
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Ichthyosis is a group of genetic skin disorders that present with dry, thickened, scaly, or flaky skin. As of today, there is no cure or treatment. Doctors can only treat the dry skin with different types of emollients to soften the scale. A deeper understanding of this disease is required to develop better treatments. There are different types of cells and cell-produced signals (biomarkers) that are being studied in order to help find these new treatments. Looking at biomarkers has been successful in helping us to understand other skin disorders better. The purpose of this study is to determine which blood and skin biomarkers characterize ichthyosis. Hypothesis: We predict that the biomarkers correlating with disease activity in Netherton syndrome will be different than the biomarkers found to correlate with the lamellar and other ichthyosis phenotype.

Description:

Objectives: 1. To define a panel of skin and blood biomarkers associated with disease activity and pruritus in Netherton syndrome, lamellar ichthyosis, and other ichthyosis subtypes. 2. To determine if blood samples can serve as surrogates for skin immune activation and will correlate with disease severity. 3. To determine FLG, SPINK5, TGM1, or other mutation via buccal/saliva samples in ichthyosis subjects 4. To determine differences in alterations of epidermal lipids and proteins in the outer stratum corneum of epidermis collected from tape strips in patients with ichthyosis compared to the general population. There will also be a difference detected in epidermal lipids from blood samples.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: December 31, 2025
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Year to 60 Years

Eligibility

Inclusion Criteria:

• Control and ichthyosis subjects may be of either sex and must be between 1-60 years of age at the time of enrollment
• Ichthyosis subjects include individuals with a diagnosis Netherton syndrome, lamellar ichthyosis, or other ichthyosis subtypes
• Ichthyosis subjects should not have administered systemic immunosuppressant therapy in the month before the study
• Ichthyosis subjects should not use topical immunosuppressants in the week before the study
• Ichthyosis subjects should not have applied emollients to the planned biopsy sites within 12 hours before biopsy, but can be applied elsewhere
• Controls may have no inflammatory disease, atopy, or obvious xerosis (urticaria, food allergy, allergic rhinitis or conjunctivitis, asthma)
• Controls for skin sampling may have no observable abnormality in the sampled skin and, to further assure the normality of the "normal" skin edges, must not have evidence of inflammation or epidermal change in the lesion to be surgically removed
• Subjects and guardians of minors must sign the approved IRB consent form(s) prior to initiation of the study protocol

Exclusion Criteria:

• Subjects who are unable to give informed consent or assent
• Subjects who administered anti-inflammatory systemic and topical therapy or emollients that do not comply with inclusion criteria prior to blood and biopsy sampling
• Subjects whose main diagnosis is deemed unsafe by the study investigator for study participation

Related Conditions & MeSH terms

• Ichthyosis
• Ichthyosis, Lamellar
• Netherton Syndrome

Locations

Country	Name	City	State
United States	Ann & Robert H. Lurie Children's Hospital of Chicago	Chicago	Illinois
United States	Northbrook Lurie Children's Outpatient Clinic	Chicago	Illinois
United States	Northwestern University	Chicago	Illinois
United States	Icahn School of Medicine at Mount Sinai	New York	New York

Sponsors (3)

Lead Sponsor	Collaborator
Northwestern University	Galderma R&D, Icahn School of Medicine at Mount Sinai

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cellular infiltrates	We will examine your skin and blood samples for various immune cells known to be involved in ichthyosis.	One year
Primary	Gene expression	We will examine your skin and blood samples for various genes known to contribute to ichthyosis by analyzing RNA and cytokines.	One year
Secondary	Correlation of biomarkers to quality of life	We will analyze the blood and tissue biomarkers to determine whether they are comparable to quality of life and itch (pruritus) measures.	One year