ABCB1 Single-Nucleotide Polymorphisms Determine Tacrolimus Response in Patients With Ulcerative Colitis

被引:38
作者
Herrlinger, K. R. [1 ]
Koc, H. [1 ]
Winter, S. [2 ,3 ]
Teml, A. [2 ,3 ]
Stange, E. F. [1 ]
Fellermann, K. [1 ,4 ]
Fritz, P. [2 ,5 ]
Schwab, M. [2 ,6 ]
Schaeffeler, E. [2 ,3 ]
机构
[1] Robert Bosch Krankenhaus, Dept Gastroenterol Hepatol & Endocrinol, Stuttgart, Germany
[2] Dr Margarete Fischer Bosch Inst Clin Pharmacol, D-7000 Stuttgart, Germany
[3] Univ Tubingen, Tubingen, Germany
[4] Univ Hosp Schleswig Holstein, Med Clin 1, Lubeck, Germany
[5] Robert Bosch Krankenhaus, Dept Clin Pathol, Stuttgart, Germany
[6] Univ Hosp, Inst Expt & Clin Pharmacol & Toxicol, Dept Clin Pharmacol, Tubingen, Germany
关键词
RENAL-TRANSPLANT RECIPIENTS; INFLAMMATORY-BOWEL-DISEASE; P-GLYCOPROTEIN EXPRESSION; ACTIVITY IN-VIVO; MDR1; GENE; CYCLOSPORINE-A; THERAPY; FK506; PHARMACOKINETICS; DRUG;
D O I
10.1038/clpt.2010.348
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tacrolimus (Tac) is effective in the treatment of steroid-refractory ulcerative colitis (UC); however, nonresponse and unpredictable side effects are major limitations. Because Tac response in patients who have undergone solid-organ transplantation has been associated with the presence of variants in CYP3A and ABCB1, we elucidated the contributions of CYP3A4*1B and CYP3A5*3 and of ABCB1 1236C>T, 2677G>T, A, and 3435C>T polymorphisms to Tac response in 89 patients with UC. Short-term remission and response were achieved in 61 and 14% of the patients, respectively, and were associated with colectomy-free survival. In a linear logistic regression model, patients with homozygous variants for one of the three ABCB1 alleles showed significantly higher short-term remission rates as compared with those of other genotypes. The effects held true after multivariate analysis including multiple comparisons and were more pronounced after correction for dose-adjusted Tac blood trough levels. We suggest that ABCB1, but not CYP3A5, may predict short-term remission of Tac in steroid-refractory UC.
引用
收藏
页码:422 / 428
页数:7
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