4.7 Article

Identification of Transporter Polymorphisms Influencing Metformin Pharmacokinetics in Healthy Volunteers

Journal

JOURNAL OF PERSONALIZED MEDICINE
Volume 13, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/jpm13030489

Keywords

metformin; pharmacogenetics; transporters; SLC; ABC; sex; ethnicity

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For patients with type 2 diabetes, the drug metformin is commonly prescribed, but the response to this drug varies greatly among individuals. In order to study the impact of transporter variations on metformin pharmacokinetics, a study was conducted on healthy participants without confounding factors. This study is the first of its kind to consider demographic characteristics and all transporters involved in metformin distribution. The pharmacokinetic parameters of metformin were found to be influenced by age, sex, ethnicity, and several transporter polymorphisms.
For patients with type 2 diabetes, metformin is the most often recommended drug. However, there are substantial individual differences in the pharmacological response to metformin. To investigate the effect of transporter polymorphisms on metformin pharmacokinetics in an environment free of confounding variables, we conducted our study on healthy participants. This is the first investigation to consider demographic characteristics alongside all transporters involved in metformin distribution. Pharmacokinetic parameters of metformin were found to be affected by age, sex, ethnicity, and several polymorphisms. Age and SLC22A4 and SLC47A2 polymorphisms affected the area under the concentration-time curve (AUC). However, after adjusting for dose-to-weight ratio (dW), sex, age, and ethnicity, along with SLC22A3 and SLC22A4, influenced AUC. The maximum concentration was affected by age and SLC22A1, but after adjusting for dW, it was affected by sex, age, ethnicity, ABCG2, and SLC22A4. The time to reach the maximum concentration was influenced by sex, like half-life, which was also affected by SLC22A3. The volume of distribution and clearance was affected by sex, age, ethnicity and SLC22A3. Alternatively, the pharmacokinetics of metformin was unaffected by polymorphisms in ABCB1, SLC2A2, SLC22A2, or SLC47A1. Therefore, our study demonstrates that a multifactorial approach to all patient characteristics is necessary for better individualization.

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