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空腹血糖受损和葡萄糖耐量受损与正常糖耐量和糖尿病患者的脂肪细胞因子模式比较。

Adipokine pattern in subjects with impaired fasting glucose and impaired glucose tolerance in comparison to normal glucose tolerance and diabetes.

机构信息

Department of Medicine, University of Leipzig, Leipzig, Germany.

出版信息

PLoS One. 2010 Nov 9;5(11):e13911. doi: 10.1371/journal.pone.0013911.

Abstract

AIM

Altered adipokine serum concentrations early reflect impaired adipose tissue function in obese patients with type 2 diabetes (T2D). It is not entirely clear whether these adipokine alterations are already present in prediabetic states and so far there is no comprehensive adipokine panel available. Therefore, the aim of this study was to assess distinct adipokine profiles in patients with normal glucose tolerance (NGT), impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or T2D.

METHODS

Based on 75 g oral glucose tolerance tests, 124 individuals were divided into groups of IFG (n = 35), IGT (n = 45), or NGT (n = 43). Furthermore, 56 subjects with T2D were included. Serum concentrations of adiponectin, chemerin, fetuin-A, leptin, interleukin (IL)-6, retinol-binding protein 4 (RBP4), monocyte chemoattractant protein (MCP)-1, vaspin, progranulin, and soluble leptin receptor (sOBR) were measured by ELISAs.

RESULTS

Chemerin, progranulin, fetuin-A, and RBP4, IL-6, adiponectin and leptin serum concentrations were differentially regulated among the four investigated groups but only circulating chemerin was significantly different in patients with IGT compared to those with IFG. Compared to T2D the IFG subjects had higher serum chemerin, progranulin, fetuin-A and RBP4 levels which was not detectable in the comparison of the T2D and IGT group.

CONCLUSION

Alterations in adipokine serum concentrations are already detectable in prediabetic states, mainly for chemerin, and may reflect adipose tissue dysfunction as an early pathogenetic event in T2D development. In addition, distinct adipokine serum patterns in individuals with IFG and IGT suggest a specific role of adipose tissue in the pathogenesis of these prediabetic states.

摘要

目的

改变的脂肪因子血清浓度早期反映肥胖 2 型糖尿病(T2D)患者脂肪组织功能受损。目前尚不完全清楚这些脂肪因子的改变是否在糖尿病前期就已经存在,而且到目前为止还没有全面的脂肪因子检测面板。因此,本研究旨在评估糖耐量正常(NGT)、空腹血糖受损(IFG)、葡萄糖耐量受损(IGT)或 T2D 患者的不同脂肪因子谱。

方法

基于 75g 口服葡萄糖耐量试验,将 124 名个体分为 IFG(n=35)、IGT(n=45)或 NGT(n=43)组。此外,还纳入了 56 例 T2D 患者。采用 ELISA 法检测血清脂联素、趋化素、胎球蛋白 A、瘦素、白细胞介素(IL)-6、视黄醇结合蛋白 4(RBP4)、单核细胞趋化蛋白 1(MCP-1)、内脏脂肪素、颗粒蛋白前体和可溶性瘦素受体(sOBR)的浓度。

结果

在四个研究组中,趋化素、颗粒蛋白前体、胎球蛋白 A 和 RBP4、IL-6、脂联素和瘦素的血清浓度存在差异调节,但只有 IGT 患者的循环趋化素与 IFG 患者相比有显著差异。与 T2D 相比,IFG 患者的血清趋化素、颗粒蛋白前体、胎球蛋白 A 和 RBP4 水平较高,而在 T2D 和 IGT 组之间则无法检测到这些水平。

结论

在糖尿病前期,脂肪因子血清浓度的改变已经可以检测到,主要是趋化素,这可能反映了脂肪组织功能障碍作为 T2D 发病的早期发病事件。此外,IFG 和 IGT 个体的不同脂肪因子血清模式表明,脂肪组织在这些糖尿病前期状态的发病机制中具有特定作用。

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