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GWAS Study

The genetic basis of dermatophytosis skin infection susceptibility.

Haapaniemi H, Eghtedarian R, Tervi A et al.

41792138 PubMed ID
GWAS Study Type
1629323 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HH
Haapaniemi H
ER
Eghtedarian R
TA
Tervi A
VJ
Valliere J
AE
Abner E
OH
Ollila HM
Chapter II

Abstract

Summary of the research findings

Dermatophytosis is a fungal infection affecting keratinized tissues such as skin, nails, and hair, presenting as red and itchy patches, nail thickening, or hair loss. It affects around 20% of the global population but the genetic architecture remains poorly understood. We performed a genome-wide association meta-analysis of over 250,000 cases and 1.37 million controls from FinnGen, Estonian Biobank, UK Biobank, and the Million Veteran Program and identified 30 genome-wide significant loci, including seven missense variants and two loci in high linkage disequilibrium with missense variants. Top associations were near ZNF646, HLA-DQB1, FLG, FTO, SLURP2, and KRT77. Additionally, dermatophytosis subtype analyses revealed 44 signals. Our results highlight the role of disrupted keratin biology, skin barrier defects, immune dysfunction, and obesity in dermatophytosis risk. We also observed genetic overlap with other skin conditions and obesity-related traits, providing insights into disease mechanisms and potential targets for prevention and treatment.

256,822 European, African, Hispanic or Latin American and Asian ancestry cases, 1,372,501 European, African, Hispanic or Latin American and Asian ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1629323
Total Participants
GWAS
Study Type
No
Replicated
European, African unspecified, Hispanic or Latin American, Asian unspecified
Ancestry
U.S., Finland, U.K., Estonia
Recruitment Country
Chapter IV

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