硫嘌呤甲基转移酶
医学
硫唑嘌呤
基因型
内科学
不利影响
基因分型
药物遗传学
作者
Mohammed Mhanna,Munir Garaiba Gharaibeh,Mohammed Rashid,Ahmad Sharab,Mohammad Shehab,Malek Zihlif
标识
DOI:10.2174/1389200220666191021100953
摘要
Background: Inflammatory Bowel Disease (IBD) is a common disease affecting many patients. This disease is treated by azathioprine and TPMT genetic polymorphism affecting the patient’s tolerance. The aim of this study is to investigate the importance of TMPT genotyping in reducing the incidence of adverse effects of azathioprine. Methods: One hundred and forty-one IBD patients were followed for azathioprine Adverse Drug Reaction (ADR). Patients were genotyped for TPMT*2, TPMT*3A, TPMT*3B, TPMT*3C. Results: The frequency of Azathioprine adverse effect was about 35.5%. An association between TPMT genotypes 1/3A and 3B/3B and azathioprine related bone marrow suppression was found (P value ≤ 0.05). Conclusion: The findings suggest that there was a significant association between TPMT genotypes 1/3A and 3B/3B and azathioprine related bone marrow suppression.
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