Clinical Importance of Filaggrin Gene Mutation for Treatment Outcome in Atopic Dermatitis
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Purpose
Atopic dermatitis is a common disease which affects about one million people in Finland at some stage of their life. In atopic dermatitis we see a superficial inflammation of the skin and a defect in skin barrier function. The filaggrin protein plays a central role in the skin barrier function and studies indicate that about 30% of patients with atopic dermatitis have a mutation in the filaggrin gene. The aim of the study is to investigate whether a mutation in the filaggrin gene affects the clinical treatment outcome in patients with atopic dermatitis. If a mutation predisposes to a worse response to treatment, this could be examined and those patients with the mutation could be given extra treatment support for their atopic dermatitis. The prevalence of filaggrin mutation in the Finnish non-atopic population is studied in the control group.
| Condition |
|---|
|
Atopic Dermatitis |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Do Mutations in the Filaggrin Gene Have Clinical Importance for the Treatment Outcome in Atopic Dermatitis? |
- Filaggrin mutation [ Designated as safety issue: No ]
- Response to treatment [ Time Frame: 12 months ] [ Designated as safety issue: No ]
- Serum IgE [ Time Frame: 12 months ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
Serum samples are collected to investigate if the patient has a mutation in the filaggrin gene.
| Estimated Enrollment: | 800 |
| Study Start Date: | June 2011 |
| Groups/Cohorts |
|---|
| Patients with atopic dermatitis |
| Non-atopic controls |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients with atopic dermatitis who are followed-up at the Skin and Allergy Hospital in Helsinki for at least one year can be included in the study.
The control population consists of non-atopic persons without any other skin disease (samples for the control population are applied for from a sample collection of the National institute for health and welfare).
Inclusion Criteria (patients with atopic dermatitis):
- Age at least 18 years
- Clinical diagnosis of atopic dermatitis
- Need for follow-up at the Skin and Allergy Hospital
- Patient gives signed informed consent to participate in this study
- Patients parents and grandparents are of Finnish origin
Inclusion Criteria (Controls):
- No history of atopy or skin disease
- Age at least 18 years
Contacts and Locations| Contact: Anita Remitz, MD, PhD | +358-9-4711 | anita.remitz@hus.fi |
| Finland | |
| Skin and Allergy Hospital, Departments of Dermatology and Clinical Genetics | Recruiting |
| Helsinki, Finland, PB 160 | |
| Contact: Anita Remitz, MD, PhD anita.remitz@hus.fi | |
| Principal Investigator: Anita Remitz, MD, PhD | |
| Sub-Investigator: Sakari Reitamo, MD, PhD | |
| Sub-Investigator: Johanna M Mandelin, MD, PhD | |
| Sub-Investigator: Ville Kiiski, MD | |
| Sub-Investigator: Minna Pöyhönen, MD, PhD | |
| Sub-Investigator: Eveliina Salminen, MD, PhD | |
| Sub-Investigator: Sirpa Kivirikko, MD, PhD | |
| Principal Investigator: | Anita Remitz, MD, PhD | Skin and Allergy Hospital, Helsinki University Central Hospital |
More Information
No publications provided
| Responsible Party: | Anita Remitz, MD, PhD, Specialist in Dermatology, Helsinki University Central Hospital |
| ClinicalTrials.gov Identifier: | NCT01689805 History of Changes |
| Other Study ID Numbers: | FLG-255-AR |
| Study First Received: | June 23, 2011 |
| Last Updated: | September 18, 2012 |
| Health Authority: | Finland: Ministry of Social Affairs and Health |
Keywords provided by Helsinki University Central Hospital:
|
Atopic dermatitis Filaggrin |
Additional relevant MeSH terms:
|
Dermatitis Dermatitis, Atopic Skin Diseases Skin Diseases, Genetic Genetic Diseases, Inborn |
Skin Diseases, Eczematous Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 22, 2013