Circulating retinol-binding protein 4 and metabolic syndrome in the elderly

Circulating retinol-binding protein 4 and metabolic syndrome in the elderly
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DOI:
10.1007/s10354-011-0885-7
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发表时间:
2011-11-01
影响因子:
0.9
通讯作者:
Fischer, Peter
Fischer, Peter
中科院分区:
其他
文献类型:
--
作者:
Mostafaie, Nazanin;Sebesta, Christian;Fischer, Peter

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背景资料:视黄醇结合蛋白(RBP)4是一种与视黄醇特异性结合的脂肪因子,在肥胖和胰岛素抵抗之间有一定的联系,其血浆浓度可能受年龄和肥胖的影响,但只有少数研究在老年人中探讨了这种联系。因此,我们在一项老年人的大型人群队列研究(VITA)中测试了RBP 4浓度与2型糖尿病/代谢综合征(MetS)组分之间的相关性[1,2]。使用单个出生队列,本研究可以排除年龄的影响。研究方法:我们评估了RBP 4与2型糖尿病和MetS组分的相关性,包括体重指数(BMI),血压,血脂参数,空腹血糖胰岛素,稳态模型评估胰岛素抵抗(HOMA-IR),以及75-76岁参与者(N = 232)的吸烟。在本研究中,RBP 4浓度与2型糖尿病和代谢综合征(MetS)组分相关。在与RBP 4浓度相关的代谢综合征的所有个体成分中,RBP 4与血清甘油三酯的相关性和与HDL的负相关性是我们研究队列中观察到的最强的相关性(p < 0.0001)。
Background: Retinol-binding protein (RBP) 4, a human adipokine that specifically binds to retinol, has been reported to provide a link between obesity and insulin resistance.Plasma RBP4 concentration may be under the influence of age and obesity, but only a few studies has investigated this link in elderly individuals. Consequently, we tested the correlation between RBP4 concentrations and type 2 diabetes/metabolic syndrome (MetS) components in a large population based cohort study (VITA) of elderly [1, 2]. Using a single birth cohort, this investigation could exclude the influence of age. Methods: We evaluated the correlation of RBP4 with type 2 diabetes and MetS components including Body Mass Index (BMI), blood pressure, lipid parameters, fasting glucose insulin, homeostasis model assessment insulin resistance (HOMA-IR), and smoking in exclusively 75-76 year old participants (N = 232).Results: In the present study, RBP4 concentrations were associated with type 2 diabetes and metabolic syndrome (MetS) components. Of all the individual components of metabolic syndrome that were associated with RBP4 concentrations, the correlations of RBP4 with serum triglycerides and a negative correlation with HDL were the strongest ones observed in our study cohort (p < 0.0001).Conclusions: RBP4 plays a role in biological mechanisms that are responsible for insulin resistance and development of type 2 diabetes.