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衡阳地区溶质载体家族30成员8基因单核苷酸多态性与2型糖尿病的相关性研究

王建平 李晶 邓珊珊

中国全科医学2011,Vol.14Issue(12):1296-1299,4.
中国全科医学2011,Vol.14Issue(12):1296-1299,4.

衡阳地区溶质载体家族30成员8基因单核苷酸多态性与2型糖尿病的相关性研究

The Relationship between Polymorphisms of Solute Carrier Family30,Member8 Gene and Type 2 Diabetes

王建平 1李晶 2邓珊珊1

作者信息

  • 1. 421001湖南省衡阳市,南华大学附属第二医院内分泌科
  • 2. 南华大学附属南华医院内分泌科
  • 折叠

摘要

Abstract

Objective To explore the relationship between the polymorphism of rs13266634C/T of SLC30A8 gene and T2DM and IGR in Hengyang region. Methods SLC30A8 gene rs13266634 polymorphisms of 236 T2DM patients, 120 IGR patients and 218 NGT were tested by PCR - RFLP. HOMA - β and HOMA - lR were used to evaluate β - cell function and insulin resistance. Results In T2DM and IGR group , the frequencies of C allele and CC genotype of rs13266634C/T were significantly higher than those in NGT group ( P < 0. 01 ). The C allele of rs13266634C/T significantly increased T2DM and IGR risk with an allelic odd ratio ( OR ) of 1. 89 and 1. 57. than those who had T allele. HOMA - β level of the patients with CC gentype was significantly lower than those with CT and TT genotype in IGR group ( P < 0. 01 ). Conclusion ( 1 ) SLC30A8 rs13266634C/T genetic polymorphism is associated with T2DM and IGR. C allele is probahly the risk gene of T2DM. ( 2 ) SLC30A8 gene may increase the liability of T2DM by affecting the function of islet beta cell.

关键词

SLC30A8基因/多态性,单核苷酸/糖尿病,2型/糖调节受损

分类

医药卫生

引用本文复制引用

王建平,李晶,邓珊珊..衡阳地区溶质载体家族30成员8基因单核苷酸多态性与2型糖尿病的相关性研究[J].中国全科医学,2011,14(12):1296-1299,4.

基金项目

湖南省教育厅项目(09C844) (09C844)

中国全科医学

OA北大核心CSTPCD

1007-9572

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