Pharmacogenetic biomarkers of response in Crohn's disease

被引:13
作者
Linares-Pineda, T. M. [1 ]
Canadas-Garre, M. [1 ,2 ]
Sanchez-Pozo, A. [3 ]
Calleja-Hernandez, M. A. [1 ]
机构
[1] Complejo Hosp Univ Granada, UGC Prov Farm Granada, Pharmacogenet Unit, Inst Invest Biosanitaria Granada, Granada, Spain
[2] Queens Univ Belfast, Inst Clin Sci, Sch Med Dent & Biomed Sci, Royal Victoria Hosp,Ctr Publ Hlth, Block B,Grosvenor Rd, Belfast BT12 6BJ, Antrim, North Ireland
[3] Univ Granada, Fac Pharm, Dept Biochem, Campus Univ Cartuja, Granada, Spain
关键词
INFLAMMATORY-BOWEL-DISEASE; TUMOR-NECROSIS-FACTOR; FC-GAMMA-RIIIA; TNF-ALPHA; CHROMOSOMAL LOCATION; ULCERATIVE-COLITIS; GENE POLYMORPHISMS; INFLIXIMAB TREATMENT; SUSCEPTIBILITY LOCI; SERUM CONCENTRATION;
D O I
10.1038/tpj.2017.27
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Crohn's disease (CD) is a chronic condition, which affects the immune system. It can also affect any part of the digestive tract and be associated with external manifestations. The causes of the disease remain unknown, although it seems to be the result of a combination of factors, such as genetic predisposition, environment, lifestyle and the composition of the microbiota, among others. The treatment protocol begins with a change in eating and smoking habits, and is continued with different lines of treatment, including corticosteroids, immunomodulators and biologic therapy (infliximab and adalimumab), which have shown differences in response among patients, especially with biologic treatment. Several studies have considered the possibility that these differences in response are caused by the genetic variability of patients. Many genes have been investigated as potential predictors of response to biological drugs, such as ADAM17, ATG16L1, EMSY, CASP9, CCNY, CNTN5, FASLG, FCGR, NOD2, PTGER4, IL13, IL1B, IL27, IL11, IL17F, TNF and TNFR genes. In this review, we will gather the information on influence of gene polymorphisms investigated to date on response to biological drugs in CD patients.
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页码:1 / 13
页数:13
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