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Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.

Authors :
Fakiola M
Strange A
Cordell HJ
Miller EN
Pirinen M
Su Z
Mishra A
Mehrotra S
Monteiro GR
Band G
Bellenguez C
Dronov S
Edkins S
Freeman C
Giannoulatou E
Gray E
Hunt SE
Lacerda HG
Langford C
Pearson R
Pontes NN
Rai M
Singh SP
Smith L
Sousa O
Vukcevic D
Bramon E
Brown MA
Casas JP
Corvin A
Duncanson A
Jankowski J
Markus HS
Mathew CG
Palmer CN
Plomin R
Rautanen A
Sawcer SJ
Trembath RC
Viswanathan AC
Wood NW
Wilson ME
Deloukas P
Peltonen L
Christiansen F
Witt C
Jeronimo SM
Sundar S
Spencer CC
Blackwell JM
Donnelly P
Source :
Nature genetics [Nat Genet] 2013 Feb; Vol. 45 (2), pp. 208-13. Date of Electronic Publication: 2013 Jan 06.
Publication Year :
2013

Abstract

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.

Details

Language :
English
ISSN :
1546-1718
Volume :
45
Issue :
2
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
23291585
Full Text :
https://doi.org/10.1038/ng.2518