Defining the Skin and Blood Biomarkers of Pediatric Atopic Dermatitis SUB-STUDY: Defining the Predictive Non-Invasive Biomarkers for Pediatric Atopic Dermatitis (Funded by Regeneron Pharmaceuticals, Inc.)
概览
- 阶段
- 不适用
- 干预措施
- Control
- 疾病 / 适应症
- Atopic Dermatitis
- 发起方
- Northwestern University
- 入组人数
- 505
- 试验地点
- 8
- 主要终点
- Gene expression
- 状态
- 进行中（未招募）
- 最后更新
- 5天前
概览
简要总结
Atopic dermatitis (AD), also known as eczema, is the most common inflammatory skin disorder of children, affecting 10-20% of children and 1-2% of adults.
This skin disorder can be associated with unbearable itchiness and an increased susceptibility to skin infections. The cause of AD is currently poorly understood; therefore, there are no targeted treatment options at present. There have been recent studies in adults with AD that explain the cause and give us new routes to investigate treatment options, however no major studies in this arena have been done in children. We hope to evaluate the skin and blood biomarkers that are found in pediatric AD and compare them to adult AD.
Hypothesis: The immune system worsens the skin barrier issues that are common in atopic dermatitis. We believe there are similar immune and skin abnormalities in adult versus pediatric atopic dermatitis. Finally, blood levels of the activated molecules in atopic dermatitis can serve as surrogates for skin immune activation and will correlate with disease severity.
详细描述
Objectives: 1. To define the cellular and molecular biomarkers of atopic dermatitis in skin biopsies and blood samples from a pre-adolescent pediatric population and correlate it with disease severity. 2. To measure the skin barrier in atopic dermatitis. 3. To determine quality of life in atopic dermatitis through various questionnaires. Objectives for the non-invasive biomarkers sub-study: 1. Develop a panel of non-invasive biomarkers in tape strips and serum. 2. Correlate mRNA expression from tape-striped skin with individual markers of severity (EASI, SCORAD, pruritus and TEWL). 3. Correlate mRNA markers in blood with severity scores. 4. Correlate serum protein markers with severity scores. 5. Compare biomarkers based on patient age. 6. Correlate the biomarker candidates from tape strips and blood with the "gold standard" set of biomarkers derived from age-matched skin biopsy samples
研究者
Amy Paller
Professor and Chair of Dermatology, Professor of Pediatrics
Northwestern University
入排标准
入选标准
- •Subjects may be of either sex and must be between the ages of 0 months and 17 years at the time of enrollment (Healthy controls, atopic controls, and AD patients)
- •The skin sample and blood sample for healthy controls can have no systemic inflammatory disease or personal or familial history of atopy (hives, food allergy, allergic rhinitis or conjunctivitis, asthma)
- •The atopic blood sample controls may have an atopic condition (allergic rhinitis or asthma) but no history of atopic dermatitis
- •All 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
- •AD subjects must have mild to severe atopic dermatitis with either new onset disease within the last 6 months or with acute exacerbation of AD
- •Subjects 17 years of age and older and parents/guardians of minors must sign the approved IRB assent and consent form(s) respectively prior to initiation of the study protocol
排除标准
- •Subjects unable to give assent or parents unable to give consent due to cognitive delay or inability to understand the assent form either in writing or presented verbally (Healthy controls, atopic controls, and AD patients)
- •All subjects whose main diagnosis is deemed unsafe by the study investigator for study participation. Examples include known hemophilia or other blood disorders, or skin infection at the site of blood draw or biopsy (Healthy controls, atopic controls, and AD patients)
- •Control subjects with obvious xerosis (Healthy controls and atopic controls)
研究组 & 干预措施
Control
Healthy subjects with no history of atopy (atopic dermatitis, asthma, or allergic rhinitis) from 0 months to 17 years of age that are age and sex matched to our atopic dermatitis subjects.
Atopic Dermatitis
Children with atopic dermatitis from 0 months to 17 years of age.
Control with Atopy history
Healthy subjects from 0 months to 17 years of age with history of asthma, food allergies, or allergic rhinitis, but no atopic dermatitis or with positive family history of atopy
结局指标
主要结局
Gene expression
时间窗: One Year
We will examine skin and blood samples for various genes known to contribute to atopic dermatitis by analyzing RNA and cytokines.
Cellular infiltrates
时间窗: One year
We will examine skin and blood samples for various immune cells known to be involved in atopic dermatitis.
次要结局
- Correlation of biomarkers to quality of life(One year)