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HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants.

Authors :
Heap GA
Weedon MN
Bewshea CM
Singh A
Chen M
Satchwell JB
Vivian JP
So K
Dubois PC
Andrews JM
Annese V
Bampton P
Barnardo M
Bell S
Cole A
Connor SJ
Creed T
Cummings FR
D'Amato M
Daneshmend TK
Fedorak RN
Florin TH
Gaya DR
Greig E
Halfvarson J
Hart A
Irving PM
Jones G
Karban A
Lawrance IC
Lee JC
Lees C
Lev-Tzion R
Lindsay JO
Mansfield J
Mawdsley J
Mazhar Z
Parkes M
Parnell K
Orchard TR
Radford-Smith G
Russell RK
Reffitt D
Satsangi J
Silverberg MS
Sturniolo GC
Tremelling M
Tsianos EV
van Heel DA
Walsh A
Watermeyer G
Weersma RK
Zeissig S
Rossjohn J
Holden AL
Ahmad T
Source :
Nature genetics [Nat Genet] 2014 Oct; Vol. 46 (10), pp. 1131-4. Date of Electronic Publication: 2014 Sep 14.
Publication Year :
2014

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.

Details

Language :
English
ISSN :
1546-1718
Volume :
46
Issue :
10
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
25217962
Full Text :
https://doi.org/10.1038/ng.3093