Methotrexate pharmacogenetics in the treatment of rheumatoid arthritis

被引:35
|
作者
Jekic, Biljana [1 ]
Maksimovic, Nela [1 ]
Damnjanovic, Tatjana [1 ]
机构
[1] Univ Belgrade, Fac Med, Inst Human Genet, Belgrade 11000, Serbia
关键词
gene polymorphism; methotrexate; pharmacogenetics; rheumatoid arthritis; GAMMA-GLUTAMYL HYDROLASE; INTESTINAL FOLATE TRANSPORTER; ABCB1 C3435T POLYMORPHISM; MATRIX METALLOPROTEINASES; TISSUE INHIBITOR; MOLECULAR-CLONING; POOR RESPONSE; DOUBLE-BLIND; T-CELLS; GENE;
D O I
10.2217/pgs-2019-0121
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
For many decades, methotrexate (MXT) has remained the drug of choice in the treatment of rheumatoid arthritis (RA). Unfortunately, a considerable number of patients do not achieve an appropriate therapeutic response. Pharmacogenetics studies do not give usable results regarding differences in MTX response among RA patients. The mechanism of MTX action in RA is not completely understood. We present and discuss data regarding the molecular basis of folate and adenosine pathways, the most obvious MTX targets, to explain possible causes of therapy failure. The molecular basis of the disease could also have an impact on therapy outcomes and in this review we explore this. Finally, we make a short review of available pharmacogenetics study results.
引用
收藏
页码:1235 / 1245
页数:11
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