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Investigation of Filaggrin Gene Mutations Among Latinx Patients With Atopic Dermatitis

Atopic Dermatitis Clinical Trial

Official title:
Investigation of Filaggrin Gene Mutations Among Latinx Patients With Atopic Dermatitis

Clinical Trial Summary

The study, Investigation of Filaggrin Gene Mutations among Latinx patients with Atopic Dermatitis, will examine the association between pathogenic FLG LOF variants and AD in a new population of Latinx patients for which clinical and disease characteristics will be well-described.

Clinical Trial Description

Filaggrin deficiency is considered a major target for therapy in Atopic Dermatitis (AD).43 The current status quo with regards to FLG LOF mutations as the strongest known genetic risk factor in AD stems from incomplete data as the majority of studies that have previously examined this association have been carried out in only a limited group of populations (i.e., European ancestry).30 Such partial data impedes our full understanding of genetic risk in AD and consequently has implications for disease prognosis and management. The proposed research represents an attempt to examine long-held paradigms in AD as they relate to genetic risk factors and disease. The development of an independent cohort of Latinx subjects with physician-confirmed diagnosis of AD that is also well phenotyped and grouped by ancestry, while also capturing measures of disease severity, will provide the opportunity to examine a population that has been largely absent from prior studies and further advance our understanding of the pathogenomic role FLG LOF variants in AD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06464133
Study type Observational
Source University of Pennsylvania
Contact Jennifer Mason, MPH
Phone 215-662-7546
Email jennifer.mason1@pennmedicine.upenn.edu
Status Not yet recruiting
Phase
Start date July 15, 2024
Completion date December 31, 2027
View Details
See also
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