Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
- Resource Type
- Authors
- Mousavi, Saeedeh; Kohan, Leila; Yavarian, Majid; Habib, Asadollah
- Source
- Molecular Biology Research Communications
- Subject
- endocrine system diseases
Pharmacogenetics
SLC47A1
Short Communication
Diabetes
nutritional and metabolic diseases
Polymorphism
- Language
- English
- ISSN
- 2345-2005
2322-181X
Type 2 diabetes mellitus is a worldwide epidemic disorder with considerable health and economic consequences. Metformin is one of the most commonly prescribed oral antidiabetic drugs. Pharmacogenetic studies showed that variants in genes related to the pharmacokinetics of metformin were associated with glucose-lowering effect of metformin. The aim of this study was to evaluate pharmacogenetic variation in SLC47A1 (rs2289669) and metformin response in type 2 diabetes patients. Seventy one patients with type 2 diabetes were included in the study. The genotypes were determined by Tetra–ARMS–PCR method. There was a significant association between the study polymorphism and the response to metformin treatment with the highest HbA1C reduction in AG genotype. In the dominant model for A allele (AA+AG vs GG), patients with A allele had highest HbA1C reduction in response to metformin.