Identifying Genetic Determinants of Eczema Herpeticum and Other Viral Infections in Individuals With Atopic Dermatitis (Genetics)

National Institute of Allergy and Infectious Diseases (NIAID)

Status

Completed

Conditions

Atopic Dermatitis

Study type

Observational

Funder types

NIH

Identifiers

NCT00515047

DAIT ADVN GENE 04

HHSN266200400033

Details and patient eligibility

About

People with atopic dermatitis (AD), or eczema, are susceptible to skin infections and inflammations. Some individuals with AD develop a condition known as eczema herpeticum (EH) following exposure to the herpes simplex virus (HSV). The purpose of this study is to identify the genetic determinants that lead people with AD to develop EH and similar conditions caused by other viruses.

Full description

AD is a chronic inflammatory skin disorder characterized by recurrent viral skin infections. However, people with AD do not all develop the same infections. For example, some people with AD who receive the smallpox vaccine develop a life-threatening condition known as eczema vaccinatum (EV). This study focuses on individuals with AD who also have a history of eczema herpeticum (ADEH+), a condition similar to EV. It is unlikely that the differences in the development of skin infections are due to differences in viral exposure, and instead due to differences in each individual's response to viruses. The purpose of this study is to determine the genetic pathways which are responsible for the development of viral skin infections in people with AD.

Participants in this study will also be enrolled in the ADVN Biomarker Registry Study. There will be only one clinical visit for this study at which blood and/or skin samples may be collected. The samples will then have high-throughput genotyping to define genetic markers in individuals susceptible to viral infections.

Enrollment

900 patients

Sex

All

Ages

8 months to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Enrollment in ADVN Biomarker Registry Study
Non-Hispanic and only African American or only Caucasian race
Parent or guardian willing to provide informed consent, if necessary

Exclusion criteria

History of any systemic illness, excluding AD
Participation of a first degree relative already enrolled in the genotyping study unless the subject in question fulfills the diagnostic criteria for ADEH+. More information on this criterion can be found in the protocol.