Authors: Graham, Garry G.¹; Punt, Jeroen¹; Arora, Manit¹; Day, Richard O.¹; Doogue, Matthew P.²; Duong, Janna K.¹; Furlong, Timothy J.³; Greenfield, Jerry R.⁴; Greenup, Louise C.¹; Kirkpatrick, Carl M.⁵; Ray, John E.¹; Timmins, Peter⁶; Williams, Kenneth M.¹

Source: Clinical Pharmacokinetics, Volume 50, Number 2, 1 February 2011 , pp. 81-98(18)

Publisher: Adis International

Abstract:

Metformin is widely used for the treatment of type 2 diabetes mellitus. It is a biguanide developed from galegine, a guanidine derivative found in Galega officinalis (French lilac). Chemically, it is a hydrophilic base which exists at physiological pH as the cationic species (>99.9%). Consequently, its passive diffusion through cell membranes should be very limited. The mean ± SD fractional oral bioavailability (F) of metformin is 55 ± 16%. It is absorbed predominately from the small intestine.

Metformin is excreted unchanged in urine. The elimination half-life (t_½) of metformin during multiple dosages in patients with good renal function is approximately 5 hours. From published data on the pharmacokinetics of metformin, the population mean of its clearances were calculated. The population mean renal clearance (CL_R) and apparent total clearance after oral administration (CL/F) of metformin were estimated to be 510 ± 130 mL/min and 1140 ± 330 mL/min, respectively, in healthy subjects and diabetic patients with good renal function. Over a range of renal function, the population mean values of CL_R and CL/F of metformin are 4.3 ± 1.5 and 10.7 ± 3.5 times as great, respectively, as the clearance of creatinine (CL_CR). As the CL_R and CL/F decrease approximately in proportion to CL_CR, the dosage of metformin should be reduced in patients with renal impairment in proportion to the reduced CL_CR.

The oral absorption, hepatic uptake and renal excretion of metformin are mediated very largely by organic cation transporters (OCTs). An intron variant of OCT1 (single nucleotide polymorphism [SNP] rs622342) has been associated with a decreased effect on blood glucose in heterozygotes and a lack of effect of metformin on plasma glucose in homozygotes. An intron variant of multidrug and toxin extrusion transporter [MATE1] (G>A, SNP rs2289669) has also been associated with a small increase in antihyperglycaemic effect of metformin. Overall, the effect of structural variants of OCTs and other cation transporters on the pharmacokinetics of metformin appears small and the subsequent effects on clinical response are also limited. However, intersubject differences in the levels of expression of OCT1 and OCT3 in the liver are very large and may contribute more to the variations in the hepatic uptake and clinical effect of metformin.

Lactic acidosis is the feared adverse effect of the biguanide drugs but its incidence is very low in patients treated with metformin. We suggest that the mean plasma concentrations of metformin over a dosage interval be maintained below 2.5 mg/L in order to minimize the development of this adverse effect.

Keywords: Antihyperglycaemic, pharmacokinetics; Biguanides, pharmacokinetics; Metformin, pharmacokinetics; Pharmacogenetics

Document Type: Research article

Affiliations: 1: 1 Departments of Pharmacology & Toxicology and Medicine, St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia 2: 2 Department of Clinical Pharmacology, Flinders Medical Centre, Adelaide, South Australia, Australia 3: 3 Department of Nephrology, St Vincent's Hospital, Sydney, New South Wales, Australia 4: 4 Department of Endocrinology and Diabetes Centre, St Vincent's Hospital and Diabetes and Obesity Research Program, Garvan Institute of Medical Research, Sydney, New South Wales, Australia 5: 5 School of Pharmacy, The University of Queensland, Brisbane, Queensland, Australia 6: 6 Biopharmaceutics Research and Development, Bristol-Myers Squibb Company, Moreton, UK

Publication date: 2011-02-01

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• By this author: Graham, Garry G. ;  Punt, Jeroen ;  Arora, Manit ;  Day, Richard O. ;  Doogue, Matthew P. ;  Duong, Janna K. ;  Furlong, Timothy J. ;  Greenfield, Jerry R. ;  Greenup, Louise C. ;  Kirkpatrick, Carl M. ;  Ray, John E. ;  Timmins, Peter ;  Williams, Kenneth M.

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