Genetic variation in the visfatin (PBEF1/NAMPT) gene and type 2 diabetes in the Greek population

被引:13
|
作者
Paschou, Peristera [1 ]
Kukuvitis, Asterios [2 ]
Yavropoulou, Maria P. [3 ]
Dritsoula, Athina [1 ]
Giapoutzidis, Vasilios [3 ]
Anastasiou, Olympia [3 ]
Kazakos, Kyriakos [3 ]
Yovos, John G. [3 ]
机构
[1] Democritus Univ Thrace, Dept Mol Biol & Genet, Alexandroupolis 68100, Greece
[2] Democritus Univ Thrace, Dept Endocrinol, Alexandroupolis 68100, Greece
[3] Aristotle Univ Thessaloniki, Div Endocrinol, AHEPA Univ Hosp, GR-54006 Thessaloniki, Greece
关键词
PBEF1; NAMPT; Visfatin; Type; 2; diabetes; Genetic association; COLONY-ENHANCING FACTOR; VISCERAL FAT; OBESITY; MELLITUS; PROMOTER; GLUCOSE; HUMANS; INFLAMMATION; METABOLISM; EXPRESSION;
D O I
10.1016/j.cyto.2010.04.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Visfatin (NAMPT formerly known as PBEF1) is an adipokine that is strongly expressed in visceral fat and has caused much debate among researchers, regarding its involvement in glucose homeostasis and insulin resistance. It was initially isolated from bone marrow cells, and its involvement in inflammatory procedures such as sepsis and acute lung inflammation is now evident. Several studies have also reported an association of plasma visfatin levels with obesity. We undertook an evaluation of the involvement of the NAMPT gene in the development of type 2 diabetes (T2DM) in the Greek population. We studied 178 patients with T2DM and 177 controls that were matched for sex, age and body mass index. We genotyped three tagging SNPs selected from the HapMap II CEPH European population as reference for the Greek population. These three SNPs tag another 12 SNPs over the entire NAMPT gene with a mean r(2) of 0.92. No indications of association with disease status were found with any of the tested variants or the inferred haplotypes. Results were also negative when the quantitative traits of weight and BMI were tested. Although our study covers common variants across the NAMPT gene, the possible involvement of rare variants in T2DM etiology cannot be ruled out and will require the investigation of very large numbers of cases and controls. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 27
页数:3
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