Effect of AMP-activated protein kinase subunit alpha 2 (PRKAA2) genetic polymorphisms on susceptibility to type 2 diabetes mellitus and diabetic nephropathy in a Chinese population

被引:14
作者
Li, Qingchu [1 ,4 ,5 ]
Li, Cuilin [1 ,2 ,3 ]
Li, Haoyun [4 ,5 ]
Zeng, Liu [1 ,2 ,3 ]
Kang, Zhiqiang [4 ,5 ]
Mao, Yu [4 ,5 ]
Tang, Xinyue [1 ,2 ,3 ]
Zheng, Panpan [4 ,5 ]
He, Li [4 ,5 ]
Luo, Fang [4 ,5 ]
Li, Zhi [1 ,2 ,3 ]
机构
[1] Cent S Univ, Xiangya Hosp, Dept Clin Pharmacol, Xiangya Rd 110, Changsha 410078, Hunan, Peoples R China
[2] Cent S Univ, Inst Clin Pharmacol, Changsha, Hunan, Peoples R China
[3] Hunan Key Lab Pharmacogenet, Changsha, Hunan, Peoples R China
[4] Zhengzhou Univ, Dept Key Lab Endocrinol, Zhengzhou Cent Hosp, Zhengzhou, Henan, Peoples R China
[5] Zhengzhou Univ, Dept Med Ctr Transformat, Zhengzhou Cent Hosp, Zhengzhou, Peoples R China
关键词
AMP-activated protein kinase subunit alpha 2 (PRKAA2); diabetic nephropathy; polymorphism; type 2 diabetes mellitus; METABOLIC SYNDROME; HAN POPULATION; ASSOCIATION; DISEASE; METFORMIN; HEALTH;
D O I
10.1111/1753-0407.12553
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It is well known that AMP-activated protein kinase (AMPK) is a key factor affecting the development of type 2 diabetes mellitus (T2DM). The single nucleotide polymorphism (SNP) rs2746342 in the AMPK alpha 2 subunit gene (PRKAA2) has been found to be associated with susceptibility to T2DM in the Chinese Han population. The present study further investigates the association of PRKAA2 genotypes with susceptibility to T2DM and its complication, diabetic nephropathy. Methods: The PRKAA2 genotypes of 406 T2DM patients and 214 controls from the Chinese Han population were determined with regard to SNPs rs10789038, rs2796498 and rs2746342. The association between these SNPs and susceptibility to T2DM and diabetic nephropathy was evaluated. The clinical characteristics differed significantly between T2DM patients and controls. Results: After adjustment for age, sex and body mass index, there was an obvious relationship between T2DM and both rs10789038 (odds ratio [OR] 1.634; P = 0.015) and rs2796498 (OR 0.656; P = 0.030), but not rs2746342. There was haplotype association of PRKAA2 rs10789038-rs2796498-rs2746342 with T2DM susceptibility. In addition, rs2796498 was found to be related to the susceptibility to diabetic nephropathy. Conclusions: Polymorphisms in rs10789038 and rs2796498 are associated with the susceptibility to T2DM, and rs2796498 may be related to diabetic nephropathy.
引用
收藏
页码:43 / 49
页数:7
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