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多药耐药基因MDR1C1236T多态性与炎症性肠病患者的活性代谢物6-TGNs的相关性

冯静 陈瑜君 王雪丁 黄民 高翔 胡品津 李嘉丽 陈旻湖 陈白莉 何瑶 张羽 龙顺华

中国临床药理学杂志2012,Vol.28Issue(5):333-337,5.
中国临床药理学杂志2012,Vol.28Issue(5):333-337,5.

多药耐药基因MDR1C1236T多态性与炎症性肠病患者的活性代谢物6-TGNs的相关性

Relationship between MDR1C1236T polymorphism and active metabolite of 6-thioguanine nucleotide in patients with the inflammatory bowel disease

冯静 1陈瑜君 2王雪丁 1黄民 1高翔 2胡品津 2李嘉丽 1陈旻湖 2陈白莉 2何瑶 2张羽 1龙顺华2

作者信息

  • 1. 中山大学药学院临床药理研究所,广州510080
  • 2. 中山大学附属第一医院消化科,广州510080
  • 折叠

摘要

Abstract

Objective To investigate the relationship between multidrug resistance gene (MDR1) C1236T and 6 - thioguanine nucleotide concentrations (6 -TGNs) and thiopurine - induced adverse effects in patients with inflammatory bowel disease (IBD). Methods Blood samples and clinical data were collected from a cohort of 105 unrelated Chinese IBD patients who were receiving azathioprine ( AZA)/6 - mereaptopurine (6 -MP) therapy. MDR1C1236T genotype was detected by polymerase chain reaction and restriction fragment length polymorphism ( PCR -RFLP) , and erythrocyte 6 - TGNs were determined by HPLC. The associations between MDR1 C1236T genotype and 6 - TGNs level/adverse effects were evaluated using chi - square test Results 6 - TGNs concentration was found higher in 1236 TT/CT carriers than that in 1236CC carriers treated with the same dose of AZA/6 - MP(P =0. 048). Meanwhile, a positive correlation between 1236CT/TT and adverse effects was found in IBD patients ( P - 0. 045 ). Conclusion MDR1 1236 C > T mutants play important role in higher 6 - TGNs concentration and higher incidence of adverse reactions.

关键词

多药耐药蛋白/基因多态性/炎症性肠病/6-硫鸟苷酸

Key words

multidrug resistance protein/ gene polymorphism/ inflammatory bowel disease/ 6 - thioguanine nucleotide

分类

医药卫生

引用本文复制引用

冯静,陈瑜君,王雪丁,黄民,高翔,胡品津,李嘉丽,陈旻湖,陈白莉,何瑶,张羽,龙顺华..多药耐药基因MDR1C1236T多态性与炎症性肠病患者的活性代谢物6-TGNs的相关性[J].中国临床药理学杂志,2012,28(5):333-337,5.

基金项目

国家自然科学基金资助项目(81072708 ()

81173131 ()

81102515) ()

中国临床药理学杂志

OA北大核心CSCDCSTPCD

1001-6821

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