Characterization of Lipoprotein Composition and Function in Pediatric Psoriasis Before and After Treatment



Status:Recruiting
Conditions:Psoriasis
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:6 - 17
Updated:1/3/2019
Start Date:December 1, 2018
End Date:December 2020
Contact:DermatologyCTU
Email:NUderm-research@northwestern.edu
Phone:312-503-5944

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This study will assess differences in inflammatory proteins, lipoprotein composition,
cholesterol efflux and HDL-proteome in moderate-to-severe pediatric psoriasis who at baseline
begin systemically administered therapy vs: a) healthy controls; and b) patients with milder
psoriasis.


Inclusion Criteria:

- Children ages 6-17 years of all races/ethnicities with plaque and/or extensive guttate
psoriasis for at least 6 months and on topical or systemic therapy

- Patients in the systemic group can be starting a medication for the first time OR
transitioning from another systemic if unresponsive and on that previous treatment for
≤ 3 months.

- Patients may concurrently have psoriatic arthritis if initiation of a systemic
medication is warranted by skin severity.

- Children ages 6-17 years of all races/ethnicities with acne being treated with
isotretinoin

- Children ages 6-17 years of all races/ethnicities without plaque or guttate psoriasis
and history of severe acne or treatment with isotretinoin as controls.

Exclusion Criteria:

- Patients less than 6 years of age or 18 years and older

- Patients with congenital heart disease, prior cardiac catheterizations/surgeries, or
on cardiac medications in the past two years other than for hypertension (eg, calcium
channel-blockers, beta-blockers and vasotropic medications).

- Patients who have other systemic inflammatory diseases (including atopic dermatitis,
severe acne, inflammatory bowel disease, juvenile idiopathic arthritis, connective
tissue diseases and/or other autoimmune diseases).

- Patients who have active infection or malignancy or have suffered from infection
requiring oral or parenteral antibiotic in past 2 weeks.

- Patients and parents/caregivers unable to give written informed consent.
We found this trial at
1
site
225 E Chicago Ave
Chicago, Illinois 60611
(312) 227-4000
Principal Investigator: Amy Paller, MD
Phone: 312-503-5944
Ann & Robert H. Lurie Children's Hospital of Chicago Ann & Robert H. Lurie Children
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mi
from
Chicago, IL
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