Heap Graham A, Weedon Michael N, Bewshea Claire M, Singh Abhey, Chen Mian, Satchwell Jack B, Vivian Julian P, So Kenji, Dubois Patrick C, Andrews Jane M, Annese Vito, Bampton Peter, Barnardo Martin, Bell Sally, Cole Andy, Connor Susan J, Creed Tom, Cummings Fraser R, D'Amato Mauro, Daneshmend Tawfique K, Fedorak Richard N, Florin Timothy H, Gaya Daniel R, Greig Emma, Halfvarson Jonas, Hart Alisa, Irving Peter M, Jones Gareth, Karban Amir, Lawrance Ian C, Lee James C, Lees Charlie, Lev-Tzion Raffi, Lindsay James O, Mansfield John, Mawdsley Joel, Mazhar Zia, Parkes Miles, Parnell Kirstie, Orchard Timothy R, Radford-Smith Graham, Russell Richard K, Reffitt David, Satsangi Jack, Silverberg Mark S, Sturniolo Giacomo C, Tremelling Mark, Tsianos Epameinondas V, van Heel David A, Walsh Alissa, Watermeyer Gill, Weersma Rinse K, Zeissig Sebastian, Rossjohn Jamie, Holden Arthur L, Ahmad Tariq
1] IBD Pharmacogenetics, Royal Devon and Exeter Hospital, Exeter, UK. [2] Precision Medicine Exeter, University of Exeter, Exeter, UK. [3].
1] Precision Medicine Exeter, University of Exeter, Exeter, UK. [2].
Nat Genet. 2014 Oct;46(10):1131-4. doi: 10.1038/ng.3093. Epub 2014 Sep 14.
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-DQA102:01-HLA-DRB107:01 haplotype. Patients heterozygous at rs2647087 have a 9% risk of developing pancreatitis after administration of a thiopurine, whereas homozygotes have a 17% risk.
接受硫唑嘌呤或巯嘌呤治疗的患者中,约4%会发生胰腺炎。其发病不可预测,几乎总会导致停药。我们从全球168个地点确定了在开始使用这些药物后3个月内发生胰腺炎的炎症性肠病(IBD)患者。经过详细的病例判定后,我们对172例IBD病例和2035例IBD对照进行了全基因组关联研究。我们在II类HLA区域发现了强烈的关联证据,在rs2647087处发现了最显著的关联(比值比2.59,95%置信区间2.07 - 3.26,P = 2×10⁻¹⁶)。我们在一组独立的78例IBD病例和472例与药物暴露匹配的IBD对照中重复了这些发现。对HLA区域的精细定位确定了与HLA - DQA102:01 - HLA - DRB107:01单倍型的关联。rs2647087位点杂合的患者在服用硫唑嘌呤后发生胰腺炎的风险为9%,而纯合子的风险为17%。