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Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients

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 w...

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Autores principales: Mousavi, Saeedeh, Kohan, Leila, Yavarian, Majid, Habib, Asadollah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534524/
https://www.ncbi.nlm.nih.gov/pubmed/28775995
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author Mousavi, Saeedeh
Kohan, Leila
Yavarian, Majid
Habib, Asadollah
author_facet Mousavi, Saeedeh
Kohan, Leila
Yavarian, Majid
Habib, Asadollah
author_sort Mousavi, Saeedeh
collection PubMed
description 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.
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spelling pubmed-55345242017-08-03 Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients Mousavi, Saeedeh Kohan, Leila Yavarian, Majid Habib, Asadollah Mol Biol Res Commun Short Communication 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. Shiraz University 2017-06 /pmc/articles/PMC5534524/ /pubmed/28775995 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Mousavi, Saeedeh
Kohan, Leila
Yavarian, Majid
Habib, Asadollah
Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title_full Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title_fullStr Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title_full_unstemmed Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title_short Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
title_sort pharmacogenetic variation of slc47a1 gene and metformin response in type2 diabetes patients
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534524/
https://www.ncbi.nlm.nih.gov/pubmed/28775995
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