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Disease Trajectories and Anti-cytokine Response Signatures in Atopic Dermatitis and Psoriasis

Recruiting
Conditions
Atopic Dermatitis
Healthy
Psoriasis
Interventions
Other: Biosampling for molecular analysis
Registration Number
NCT03361215
Lead Sponsor
University Hospital Schleswig-Holstein
Brief Summary

The clinical study investigates the long-term course of disease in patients with chronic inflammatory skin diseases (atopic eczema and psoriasis) and the impact of tarheted therapies on the clinical and molecular level. For this purpose, patients are asked to take part in regular examinations and data collections, and to donate biomaterials (blood, skin biopsies, skin swabs, tape strips, stool samples). Blood samples are used to analyze inflammation messengers. Punch biopsies from lesional and non-lesional skin areas are used to analyze gene expression. Tape strips are pieces of transparent adhesive tapes to strip off most of the horny layer that will be used to examine mRNA and protein expression. The skin smears are superficial smears of three areas of skin with cotton swabs, which are used to examine bacteria on the skin. Overall, the study will help to monitor the disease course clinically and on the molecular level in participating patients for at least ten years and to collect information about the impact of various external factors including treatments. The study has no effect on the therapies of the disease, it serves only the accompanying data collection

Detailed Description

Atopic dermatitis and psoriasis are the most common chronic inflammatory skin diseases in dermatology. Due to genetic predispositions, inflammatory changes of the skin occur. The specific mechanisms are only partly understood for both diseases and targeted therapies are established in psoriasis therapy and are becoming available for atopic dermatitis. In order to better understand the course of the disease and to characterize the changes in the inflammatory mechanisms during the course of the disease and under the influence of external factors such as therapies, longitudinal prospective studies are needed to evaluate clinical data and biological samples. This study investigates long-term clinical and epidemiological data from affected patients, as well as biological samples, including blood samples, skin biopsies, non-invasive skin swabs for microbiome detection, and tape strips for the molecular characterization of the disease. Data collection and biosampling will be done during routine visits, typically at week 0, 2, 12 and 52.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1000
Inclusion Criteria
  • Patients with a clinical diagnosis of atopic dermatitis, psoriasis or autoimmune skin disease
  • Written informed consent obtained from the subject
Exclusion Criteria
  • Patients who decline participation

In patients<18 years of age no biopsies will be taken

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
ControlsBiosampling for molecular analysisHealthy volunteers with no history of atopic, autoimmune or chronic inflammatory disease.
Atopic dermatitisBiosampling for molecular analysisPatients with dermatologist-diagnosed atopic dermatitis, psoriasis or autoimmune skin disease.
Primary Outcome Measures
NameTimeMethod
Disease progression10 years

Epidemiological and phenotypical data of patients

Molecular signature changes10 years

Molecular signatures will be measured using OMICS and sequencing technologies

Secondary Outcome Measures
NameTimeMethod
Development of comorbidities10 years

Assessment of newly developed comorbid diseases over time

Trial Locations

Locations (1)

Department of Dermatology, University Hospital Schleswig Holstein, Campus Kiel

🇩🇪

Kiel, Germany

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