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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2011, Vol. 16 ›› Issue (11): 1315-1320.

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Progress of the pharmacokinetics of metformin in type 2 diabetes mellitus

DONG Min, LIU Zhao-qian   

  1. Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University Xiangya School of Medicine, Changsha 410078, Hunan, China
  • Received:2011-08-05 Revised:2011-10-03 Online:2011-11-26 Published:2011-11-29

Abstract: Pharmacogenetics indicates that genetic polymorphisms of drug metabolizing enzymes, receptors, and transporter are the major causes for individual difference in drug response. Metformin is regarded as insulin sensitizing drugs and the first-line agent for type 2 diabetes mellitus (T2DM) patients with overweight or obesity. Metformin is also used for treatment polycystic ovary syndrome (PCOS). Considerable individual differences in metformin efficacy are reported. Organic cation transporters (OCTS) play the important roles in the individual difference of metformin response rather than drug metabolizing enzymes and drug receptors. Thus we reviews the effects of the polymorphisms of OCTS on metformin response and the progress of the pharmacokinetics of metformin in T2DM.

Key words: Metformin, Pharmacogenetics, OCTS, Metformin response, Genetic polymorphisms

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