奥美拉唑与他克莫司在1例CYP3A5非表达者膜性肾病患者中的药理学相互作用研究

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yanli Li, Yi Liu, Zengxian Sun
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引用次数: 1

摘要

他克莫司近年来被广泛应用于膜性肾病。他克莫司与奥美拉唑合用治疗CYP3A5非表达性膜性肾病的药物相互作用尚未得到证实。在这里,我们报告了一位特发性膜性肾病患者,其CYP2C19*2/*2, CYP3A5*3/*3(非表达者)和ABCB1 (3435 TT, 1236 ct, 2677 TT)基因型需要他克莫司和奥美拉唑治疗,发现他克莫司代谢波动。本研究表明,他克莫司和奥美拉唑在CYP3A5非表达者中存在药理学药物相互作用,这意味着与他克莫司代谢相关的CYP3A和ABCB1基因突变可能会改变血液中他克莫司的水平。停止奥美拉唑治疗后,他克莫司的浓度下降。这表明,除了基因型外,临床协变量,如奥美拉唑,在更好地理解和预测他克莫司剂量时也很重要。当患者与奥美拉唑合用时,监测他克莫司血药浓度并调整剂量是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of pharmacologic interactions between omeprazole and tacrolimus in a membranous nephropathy patient with CYP3A5 nonexpresser: a case report.

Tacrolimus has been widely used in membranous nephropathy in recent years. The drug interactions of the coadministration of tacrolimus with omeprazole in CYP3A5 nonexpresser membranous nephropathy patients have not been demonstrated. Here, we report an idiopathic membranous nephropathy patient who was with CYP2C19*2/*2, CYP3A5*3/*3 (nonexpresser) and ABCB1 (3435 TT, 1236 computed tomography, 2677 TT) genotype requiring treatment with tacrolimus and omeprazole and found to have fluctuating metabolism of tacrolimus. This study shows that tacrolimus and omeprazole have pharmacologic drug interactions in CYP3A5 nonexpressers, implying that the CYP3A and ABCB1 gene mutations linked to tacrolimus metabolism may alter tacrolimus levels in the blood. The observed concentrations of tacrolimus were decreased after the discontinuation of omeprazole therapy. It demonstrates that, in addition to genotype, clinical covariates, such as omeprazole are important when it comes to better understanding and prediction of tacrolimus dosage. It is deemed necessary to monitor tacrolimus blood concentrations and make dose adjustments when patients were coadministered with omeprazole.

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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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