Takane Hiroshi, Shikata Eriko, Otsubo Kenji, Higuchi Shun, Ieiri Ichiro
Department of Pharmacy, Tottori University Hospital, Yonago, Japan.
Pharmacogenomics. 2008 Apr;9(4):415-22. doi: 10.2217/14622416.9.4.415.
Considerable interindividual variabilities in clinical efficacy and adverse events are sometimes recognized in the treatment of Type 2 diabetes mellitus with oral antihyperglycemic drugs. Metformin is the most commonly used biguanide in clinical practice, and also improves insulin resistance and reduces cardiovascular risk. However, certain patients taking metformin do not respond sufficiently. The molecular reasons for the variability in response to metformin are not clear. However, it has been recently suggested that genetic factors may be responsible for the variability. Metformin is not metabolized but is transported by at least two organic cation transporters (OCT), OCT1 and OCT2. Recently, genetic polymorphisms in OCT 1 and OCT2 have been found to be associated with changes in pharmacokinetic/pharmacodynamic responses to substrate drugs. This review focuses on the impact of the genetic polymorphism of organic cation transporters on transport activity, and the implications for the clinical efficacy of metformin.
在使用口服降糖药治疗2型糖尿病时,有时会发现临床疗效和不良事件存在相当大的个体差异。二甲双胍是临床实践中最常用的双胍类药物,还能改善胰岛素抵抗并降低心血管风险。然而,某些服用二甲双胍的患者反应并不充分。二甲双胍反应变异性的分子原因尚不清楚。然而,最近有人提出遗传因素可能是导致这种变异性的原因。二甲双胍不被代谢,但至少由两种有机阳离子转运体(OCT),即OCT1和OCT2转运。最近发现,OCT1和OCT2中的基因多态性与底物药物的药代动力学/药效学反应变化有关。本综述重点关注有机阳离子转运体基因多态性对转运活性的影响以及对二甲双胍临床疗效的影响。