Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
Jenefer Blackwell, Peter Donnelly and colleagues report a genome-wide association study for visceral leishmaniasis using studies from India and Brazil, with replication in an additional Indian study. They identify common variants at the HLA-DRB1 – HLA-DQA1 HLA class II region associated with suscept...
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Veröffentlicht in: | Nature genetics 2013-02, Vol.45 (2), p.208-213 |
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Zusammenfassung: | Jenefer Blackwell, Peter Donnelly and colleagues report a genome-wide association study for visceral leishmaniasis using studies from India and Brazil, with replication in an additional Indian study. They identify common variants at the
HLA-DRB1
–
HLA-DQA1
HLA class II region associated with susceptibility to visceral leishmaniasis.
To identify susceptibility loci for visceral leishmaniasis, we undertook genome-wide association studies in two populations: 989 cases and 1,089 controls from India and 357 cases in 308 Brazilian families (1,970 individuals). The
HLA-DRB1
–
HLA-DQA1
locus was the only region to show strong evidence of association in both populations. Replication at this region was undertaken in a second Indian population comprising 941 cases and 990 controls, and combined analysis across the three cohorts for rs9271858 at this locus showed
P
combined
= 2.76 × 10
−17
and odds ratio (OR) = 1.41, 95% confidence interval (CI) = 1.30–1.52. A conditional analysis provided evidence for multiple associations within the
HLA-DRB1
–
HLA-DQA1
region, and a model in which risk differed between three groups of haplotypes better explained the signal and was significant in the Indian discovery and replication cohorts. In conclusion, the
HLA-DRB1
–
HLA-DQA1
HLA class II region contributes to visceral leishmaniasis susceptibility in India and Brazil, suggesting shared genetic risk factors for visceral leishmaniasis that cross the epidemiological divides of geography and parasite species. |
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ISSN: | 1061-4036 1546-1718 |
DOI: | 10.1038/ng.2518 |