Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/102753
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Type: Journal article
Title: HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Author: Heap, G.
Weedon, M.
Bewshea, C.
Singh, A.
Chen, M.
Satchwell, J.
Vivian, J.
So, K.
Dubois, P.
Andrews, J.
Annese, V.
Bampton, P.
Barnardo, M.
Bell, S.
Cole, A.
Connor, S.
Creed, T.
Cummings, F.
D'Amato, M.
Daneshmend, T.
et al.
Citation: Nature Genetics, 2014; 46(10):1131-1134
Publisher: Nature Publishing Group
Issue Date: 2014
ISSN: 1061-4036
1546-1718
Statement of
Responsibility: 
Graham A. Heap ... Jane M. Andrews ... et al.
Abstract: Pancreatitis occurs in approximately 4% of patients treated with the thiopurines azathioprine or mercaptopurine. Its development is unpredictable and almost always leads to drug withdrawal. We identified patients with inflammatory bowel disease (IBD) who had developed pancreatitis within 3 months of starting these drugs from 168 sites around the world. After detailed case adjudication, we performed a genome-wide association study on 172 cases and 2,035 controls with IBD. We identified strong evidence of association within the class II HLA region, with the most significant association identified at rs2647087 (odds ratio 2.59, 95% confidence interval 2.07-3.26, P = 2 × 10⁻¹⁶). We replicated these findings in an independent set of 78 cases and 472 controls with IBD matched for drug exposure. Fine mapping of the HLA region identified association with the HLA-DQA1*02:01-HLA-DRB1*07:01 haplotype. Patients heterozygous at rs2647087 have a 9% risk of developing pancreatitis after administration of a thiopurine, whereas homozygotes have a 17% risk.
Keywords: Pancreatitis; thiopurine immunosuppressants
Rights: © 2014 Nature America, Inc. All rights reserved.P
RMID: 0030027981
DOI: 10.1038/ng.3093
Appears in Collections:Medicine publications

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