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Association of genetic polymorphisms in SLC22A1 and SLC22A2 with intolerance to metformin in type 2 diabetes |
FU Ting1,2,SHI Jiandang3,KUANG Xia2,and WANG Suli1,2 |
1.Department of Internal Medicine,Hebei Medical University,Shijiazhuang 050000,China; 2.Department of Endocrinology,The Affiliated Hospital of Logistics University of Chinese People’s Armed Police Force,Tianjin 300162,China; 3.College of Life Sciences,Nankai University, Tianjin 300017, China |
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Abstract Objective To study the relationship between gene polymorphisms of 1222A>G in SLC22A1 and 808G>T in SLC22A2 with the gastrointestinal side-effects in metformin-treated type 2 diabetes patients.Methods One hundred and thirty type 2 diabetes patients treated with metformin at the first time were recruited.Genomic DNA samples were extracted from the patients’ leukocytes in the peripheral blood.The genotypes were determined by the allele-specific polymerase chain reaction(AS-PCR)and gel electrophoresismethod.Results Three genotypes of AA, AG, GG were found in SLC22A11222A>G site and the mutation frequency was 64.62%.An allele of 1222A>G was associated with the incidence of gastrointestinal side-effects of metformin(P<0.05).Three genotypes of GG, GT, TT were found in SLC22A2 808G>T site and the mutation frequency was 11.15%.The incidence of gastrointestinal side effects in metformin-treated type 2 diabetes patients with different genotypes had no significant differences(P=0.559).The patients in metformin intolerance group were older than the patients in metformin tolerance group. The patients in metformin intolerance group had higher systolic blood pressure than the patients in metformin tolerance group.Conclusions SLC22A11222A>G gene polymorphis was associated with the incidence of gastrointestinal side effects in metformin-treated type 2 diabetes patients, however SLC22A2 808G>T is not.Older age and high systolic blood pressure may be the risk factors for metformin intolerance.
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Received: 11 November 2015
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