4.8 Article

HLA Class II Locus and Susceptibility to Podoconiosis

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 366, Issue 13, Pages 1200-1208

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1108448

Keywords

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Funding

  1. Wellcome Trust [079791]
  2. Association of Physicians of Great Britain and Ireland
  3. Center for Research on Genomics and Global Health (CRGGH)
  4. National Human Genome Research Institute
  5. National Institute of Diabetes and Digestive and Kidney Diseases
  6. Center for Information Technology
  7. Office of the Director at the National Institutes of Health [Z01HG200362]

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BACKGROUND Podoconiosis is a tropical lymphedema resulting from long-term barefoot exposure to red-clay soil derived from volcanic rock. The World Health Organization recently designated it as a neglected tropical disease. Podoconiosis develops in only a subgroup of exposed people, and studies have shown familial clustering with high heritability (63%). METHODS We conducted a genomewide association study of 194 case patients and 203 controls from southern Ethiopia. Findings were validated by means of family-based association testing in 202 family trios and HLA typing in 94 case patients and 94 controls. RESULTS We found a genomewide significant association of podoconiosis with the single-nucleotide polymorphism (SNP) rs17612858, located 5.8 kb from the HLA-DQA1 locus (in the allelic model: odds ratio, 2.44; 95% confidence interval [CI], 1.82 to 3.26; P = 1.42x10(-9); and in the additive model: odds ratio, 2.19; 95% CI, 1.66 to 2.90; P = 3.44x10(-8)), and suggestive associations (P<1.0x10(-5)) with seven other SNPs in or near HLA-DQB1, HLA-DQA1, and HLA-DRB1. We confirmed these associations using family-based association testing. HLA typing showed the alleles HLA-DRB1*0701 (odds ratio, 2.00), DQA1*0201 (odds ratio, 1.91), and DQB1*0202 (odds ratio, 1.79) and the HLA-DRB1*0701-DQB1*0202 haplotype (odds ratio, 1.92) were risk variants for podoconiosis. CONCLUSIONS Association between variants in HLA class II loci with podoconiosis (a noncommunicable disease) suggests that the condition may be a T-cell-mediated inflammatory disease and is a model for gene-environment interactions that may be relevant to other complex genetic disorders. (Funded by the Wellcome Trust and others.)

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