Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups

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作者
Tewodros Gebresilase
Chris Finan
Daniel Suveges
Tesfaye Sisay Tessema
Abraham Aseffa
Gail Davey
Konstantinos Hatzikotoulas
Eleftheria Zeggini
Melanie J. Newport
Fasil Tekola-Ayele
机构
[1] Armauer Hansen Research Institute (AHRI),Unit of Health Biotechnology, Institute of Biotechnology, College of Natural and Computational Sciences
[2] Addis Ababa University,Institute of Cardiovascular Science, Faculty of Population Health
[3] University College London,Brighton and Sussex Centre for Global Health Research
[4] Wellcome Trust Sanger Institute,Epidemiology Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development
[5] Brighton and Sussex Medical School,Institute of Translational Genomics
[6] National Institutes of Health,TUM School of Medicine
[7] European Bioinformatics Institute,undefined
[8] Helmholtz Zentrum München – German Research Center for Environmental Health,undefined
[9] Technical University of Munich and Klinikum Rechts Der Isar,undefined
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Podoconiosis, a debilitating lymphoedema of the leg, results from barefoot exposure to volcanic clay soil in genetically susceptible individuals. A previous genome-wide association study (GWAS) conducted in the Wolaita ethnic group from Ethiopia showed association between single nucleotide polymorphisms (SNPs) in the HLA class II region and podoconiosis. We aimed to conduct a second GWAS in a new sample (N = 1892) collected from the Wolaita and two other Ethiopian populations, the Amhara and the Oromo, also affected by podoconiosis. Fourteen SNPs in the HLA class II region showed significant genome-wide association (P < 5.0 × 10−8) with podoconiosis. The lead SNP was rs9270911 (P = 5.51 × 10−10; OR 1.53; 95% CI 1.34–1.74), located near HLA-DRB1. Inclusion of data from the first GWAS (combined N = 2289) identified 47 SNPs in the class II HLA region that were significantly associated with podoconiosis (lead SNP also rs9270911 (P = 2.25 × 10−12). No new loci outside of the HLA class II region were identified in this more highly-powered second GWAS. Our findings confirm the HLA class II association with podoconiosis suggesting HLA-mediated abnormal induction and regulation of immune responses may have a direct role in its pathogenesis.
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