Optimizing Thiopurine Therapy in Inflammatory Bowel Disease

被引:30
|
作者
Chevaux, Jean-Baptiste [2 ,3 ]
Peyrin-Biroulet, Laurent [2 ,3 ]
Sparrow, Miles P. [1 ]
机构
[1] Alfred Hosp, Dept Gastroenterol, Melbourne, Vic, Australia
[2] Univ Hosp Nancy, Dept Hepatogastroenterol, Vandoeuvre Les Nancy, France
[3] Univ Hosp Nancy, INSERM, U954, Vandoeuvre Les Nancy, France
关键词
thiopurines; optimization; inflammatory bowel disease; ADVERSE DRUG-REACTIONS; CROHNS-DISEASE; AZATHIOPRINE THERAPY; XANTHINE-OXIDASE; METHYLTRANSFERASE ACTIVITY; S-METHYLTRANSFERASE; COMBINATION THERAPY; ULCERATIVE-COLITIS; 6-MERCAPTOPURINE; ALLOPURINOL;
D O I
10.1002/ibd.21494
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite recent advances, the therapeutic armamentarium for inflammatory bowel disease (IBD) is still limited. In addition, a step-up approach is recommended for most IBD patients. Thus, optimizing each medical therapy before switching to another drug class is the rule in clinical practice. Conventional therapies for IBD have not received the same amount of attention as biologic therapies over the last decade. However, due to their efficacy, safety, and low cost the thiopurine drugs azathioprine and 6-mercaptopurine remain the backbone of therapy for IBD. Pharmacogenomic advances and increased knowledge of their metabolism are allowing dosage optimization. Herein, after describing the pharmacogenetics and pharmacokinetics of thiopurines, we will discuss how to optimize thiopurine therapy. We will then underscore the need to take into account safety issues when optimizing thiopurine treatment.
引用
收藏
页码:1428 / 1435
页数:8
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