Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China; The Affiliated Hospital, School of Medicine, Ningbo University, Ningbo, Zhejiang 315000, China; Diabetes Center, School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China.
Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China.
Gene. 2014 Sep 1;547(2):329-33. doi: 10.1016/j.gene.2014.06.062. Epub 2014 Jun 30.
The GCK gene encodes hexokinase 4, which catalyzes the first step in most glucose metabolism pathways. The purpose of our study is to assess the contribution of GCK methylation to type 2 diabetes (T2D).
GCK methylation was evaluated in 48 T2D cases and 48 age- and gender-matched controls using the bisulphite pyrosequencing technology. Among the four CpG sites in the methylation assay, CpG4 and the other three CpGs (CpG1-3) were not in high correlation (r<0.5). Significantly elevated methylation levels of GCK CpG4 methylation were observed in T2D patients than in the healthy controls (P=0.004). A breakdown analysis by gender indicated that the association between CpG4 methylation and T2D was specific to males (P=0.002). It is intriguing that another significant male-specific association was also found between GCK CpG4 methylation and total cholesterol (TC) concentration (r=0.304, P=0.036).
Our results showed that elevated GCK CpG4 methylation might suggest a risk of T2D in Chinese males. Gender disparity in GCK CpG4 methylation might provide a clue to elaborate the pathogenesis of T2D.
GCK 基因编码己糖激酶 4,该酶催化大多数葡萄糖代谢途径的第一步。我们研究的目的是评估 GCK 甲基化对 2 型糖尿病(T2D)的贡献。
采用亚硫酸氢盐焦磷酸测序技术评估了 48 例 T2D 病例和 48 例年龄和性别匹配的对照者的 GCK 甲基化情况。在甲基化测定的四个 CpG 位点中,CpG4 与其他三个 CpG(CpG1-3)相关性不强(r<0.5)。与健康对照组相比,T2D 患者的 GCK CpG4 甲基化水平显著升高(P=0.004)。按性别进行细分分析表明,CpG4 甲基化与 T2D 之间的关联仅存在于男性(P=0.002)。有趣的是,还发现 GCK CpG4 甲基化与总胆固醇(TC)浓度之间存在另一个显著的男性特异性关联(r=0.304,P=0.036)。
我们的结果表明,升高的 GCK CpG4 甲基化可能提示中国男性患 T2D 的风险增加。GCK CpG4 甲基化的性别差异可能为阐述 T2D 的发病机制提供线索。