Abstract
UDP-glucuronosyltransferase 1A6 (UGT1A6) is involved in metabolizing non-steroidal anti-inflammatory drugs (NSAIDs). Genotype variation in UGT1A6 may influence the metabolism of NSAIDs and we studied whether this might modulate the gastrointestinal toxicity of NSAIDs. UGT1A6 genotypes of 114 patients with peptic ulcer haemorrhage were compared with those of two subsets of controls: 158 cardiology patients using similar amounts of NSAIDs and 140 healthy controls, hardly using NSAIDs. Risk factors for peptic ulcer bleeding were male gender (Odds ratio (OR) 2.66, 95% confidence interval (CI) 1.7-4.2), age above 60 years (OR 2.15, 95% CI 1.4-3.4) and use of NSAIDs/aspirin (OR 4.50, 95% CI 2.8-7.3). UGT1A6 genotype frequencies did not differ between patients with peptic ulcer and the two control groups (p=0.76). We conclude that polymorphic UGT1A6 is not implicated in the pathogenesis of NSAIDs-related peptic ulcer disease.
Keywords: UDP-glucuronosyltransferase 1A6, upper gastrointestinal symptoms, upper gastrointestinal bleeding, non-steroidal anti-inflammatory drugs, aspirin, genetic polymorphism
Drug Metabolism Letters
Title: Genetic Polymorphisms in UDP-Glucuronosyltransferase 1A6 Are Not Associated with NSAIDs-Related Peptic Ulcer Haemorrhage
Volume: 3 Issue: 3
Author(s): Martijn G.H. van Oijen, Marjolein I.A. Koetsier, Robert J.F. Laheij, Hennie M.J. Roelofs, Rene H.M. te Morsche, Wilbert H.M. Peters, Freek W.A. Verheugt, Jan B.M.J. Jansen and Joost P.H. Drenth
Affiliation:
Keywords: UDP-glucuronosyltransferase 1A6, upper gastrointestinal symptoms, upper gastrointestinal bleeding, non-steroidal anti-inflammatory drugs, aspirin, genetic polymorphism
Abstract: UDP-glucuronosyltransferase 1A6 (UGT1A6) is involved in metabolizing non-steroidal anti-inflammatory drugs (NSAIDs). Genotype variation in UGT1A6 may influence the metabolism of NSAIDs and we studied whether this might modulate the gastrointestinal toxicity of NSAIDs. UGT1A6 genotypes of 114 patients with peptic ulcer haemorrhage were compared with those of two subsets of controls: 158 cardiology patients using similar amounts of NSAIDs and 140 healthy controls, hardly using NSAIDs. Risk factors for peptic ulcer bleeding were male gender (Odds ratio (OR) 2.66, 95% confidence interval (CI) 1.7-4.2), age above 60 years (OR 2.15, 95% CI 1.4-3.4) and use of NSAIDs/aspirin (OR 4.50, 95% CI 2.8-7.3). UGT1A6 genotype frequencies did not differ between patients with peptic ulcer and the two control groups (p=0.76). We conclude that polymorphic UGT1A6 is not implicated in the pathogenesis of NSAIDs-related peptic ulcer disease.
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Cite this article as:
van Oijen G.H. Martijn, Koetsier I.A. Marjolein, Laheij J.F. Robert, Roelofs M.J. Hennie, te Morsche H.M. Rene, Peters H.M. Wilbert, Verheugt W.A. Freek, Jansen B.M.J. Jan and Drenth P.H. Joost, Genetic Polymorphisms in UDP-Glucuronosyltransferase 1A6 Are Not Associated with NSAIDs-Related Peptic Ulcer Haemorrhage, Drug Metabolism Letters 2009; 3(3) . https://dx.doi.org/10.2174/187231209789352111
DOI https://dx.doi.org/10.2174/187231209789352111 |
Print ISSN 1872-3128 |
Publisher Name Bentham Science Publisher |
Online ISSN 1874-0758 |

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