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HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease
The immunosuppressant drug azathioprine is associated with a 4% risk of acute pancreatitis in patients with inflammatory bowel disease (IBD). Studies have demonstrated an increased risk in carriers of HLA‐DQA1*02:01 and HLA‐DRB1*07:01. We investigated whether these human leukocyte antigen (HLA) type...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099136/ https://www.ncbi.nlm.nih.gov/pubmed/35120281 http://dx.doi.org/10.1111/cts.13244 |
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author | Ås, Joel Bertulyte, Ilma Eriksson, Niclas Magnusson, Patrik K.E. Wadelius, Mia Hallberg, Pär |
author_facet | Ås, Joel Bertulyte, Ilma Eriksson, Niclas Magnusson, Patrik K.E. Wadelius, Mia Hallberg, Pär |
author_sort | Ås, Joel |
collection | PubMed |
description | The immunosuppressant drug azathioprine is associated with a 4% risk of acute pancreatitis in patients with inflammatory bowel disease (IBD). Studies have demonstrated an increased risk in carriers of HLA‐DQA1*02:01 and HLA‐DRB1*07:01. We investigated whether these human leukocyte antigen (HLA) types were associated with azathioprine‐induced pancreatitis also in Swedish patients with IBD, and whether the type of disease affected the association. Nineteen individuals with IBD who developed acute pancreatitis after initiation of azathioprine were genotyped and compared with a population control cohort (n = 4891) and a control group matched for disease (n = 81). HLA‐DQA1*02:01 and HLA‐DRB1*07:01 were in full linkage disequilibrium, and were significantly associated with acute pancreatitis both when cases were compared with population controls (OR 3.97 [95% CI 1.57–9.97], p = 0.0035) and matched controls (OR 3.55 [95% CI 1.23–10.98], p = 0.0275). In a disease‐specific analysis, the correlation was positive in patients with Crohn's disease versus matched controls (OR 9.27 [95% CI 1.86–46.19], p = 0.0066), but not in those with ulcerative colitis versus matched controls (OR 0.69 [95% CI 0.07–6.74], p = 0.749). In patients with Crohn's disease, we estimated the conditional risk of carriers of HLA‐DQA1*02:01‐HLA‐DRB1*07:01 to 7.3%, and the conditional risk of a non‐carrier to 2.2%. We conclude that HLA‐DQA1*02:01‐HLA‐DRB1*07:01 is a marker for increased risk of acute pancreatitis in individuals of Swedish genetic origin, treated with azathioprine for Crohn's disease. |
format | Online Article Text |
id | pubmed-9099136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90991362022-05-18 HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease Ås, Joel Bertulyte, Ilma Eriksson, Niclas Magnusson, Patrik K.E. Wadelius, Mia Hallberg, Pär Clin Transl Sci Research The immunosuppressant drug azathioprine is associated with a 4% risk of acute pancreatitis in patients with inflammatory bowel disease (IBD). Studies have demonstrated an increased risk in carriers of HLA‐DQA1*02:01 and HLA‐DRB1*07:01. We investigated whether these human leukocyte antigen (HLA) types were associated with azathioprine‐induced pancreatitis also in Swedish patients with IBD, and whether the type of disease affected the association. Nineteen individuals with IBD who developed acute pancreatitis after initiation of azathioprine were genotyped and compared with a population control cohort (n = 4891) and a control group matched for disease (n = 81). HLA‐DQA1*02:01 and HLA‐DRB1*07:01 were in full linkage disequilibrium, and were significantly associated with acute pancreatitis both when cases were compared with population controls (OR 3.97 [95% CI 1.57–9.97], p = 0.0035) and matched controls (OR 3.55 [95% CI 1.23–10.98], p = 0.0275). In a disease‐specific analysis, the correlation was positive in patients with Crohn's disease versus matched controls (OR 9.27 [95% CI 1.86–46.19], p = 0.0066), but not in those with ulcerative colitis versus matched controls (OR 0.69 [95% CI 0.07–6.74], p = 0.749). In patients with Crohn's disease, we estimated the conditional risk of carriers of HLA‐DQA1*02:01‐HLA‐DRB1*07:01 to 7.3%, and the conditional risk of a non‐carrier to 2.2%. We conclude that HLA‐DQA1*02:01‐HLA‐DRB1*07:01 is a marker for increased risk of acute pancreatitis in individuals of Swedish genetic origin, treated with azathioprine for Crohn's disease. John Wiley and Sons Inc. 2022-02-20 2022-05 /pmc/articles/PMC9099136/ /pubmed/35120281 http://dx.doi.org/10.1111/cts.13244 Text en © 2022 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Ås, Joel Bertulyte, Ilma Eriksson, Niclas Magnusson, Patrik K.E. Wadelius, Mia Hallberg, Pär HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title | HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title_full | HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title_fullStr | HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title_full_unstemmed | HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title_short | HLA variants associated with azathioprine‐induced pancreatitis in patients with Crohn’s disease |
title_sort | hla variants associated with azathioprine‐induced pancreatitis in patients with crohn’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099136/ https://www.ncbi.nlm.nih.gov/pubmed/35120281 http://dx.doi.org/10.1111/cts.13244 |
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