循环视黄醇结合蛋白4浓度可能反映胰岛素抵抗相关的铁过载。

Circulating retinol-binding protein-4 concentration might reflect insulin resistance-associated iron overload.

作者信息

Fernández-Real José Manuel, Moreno José María, Ricart Wifredo

机构信息

Diabetes, Endocrinology, and Nutrition Unit, Dr. Josep Trueta Hospital, Girona Institute for Biomedical Research, Girona, Spain.

出版信息

Diabetes. 2008 Jul;57(7):1918-25. doi: 10.2337/db08-0041. Epub 2008 Apr 21.

Abstract

OBJECTIVES

The mechanisms behind the association between retinol-binding protein-4 (RBP4) and insulin resistance are not well understood. An interaction between iron and vitamin A status, of which RBP4 is a surrogate, has long been recognized. We hypothesized that iron-associated insulin resistance could be behind the impaired insulin action caused by RBP4.

RESEARCH DESIGN AND METHODS

Serum ferritin and RBP4 concentration and insulin resistance were evaluated in a sample of middle-aged men (n = 132) and in a replication independent study. Serum RBP4 was also studied before and after iron depletion in patients with type 2 diabetes. Finally, the effect of iron on RBP4 release was evaluated in vitro in adipose tissue.

RESULTS

A positive correlation between circulating RBP4 and log serum ferritin (r = 0.35 and r = 0.61, respectively; P < 0.0001) was observed in both independent studies. Serum RBP4 concentration was higher in men than women in parallel to increased ferritin levels. On multiple regression analyses to predict serum RBP4, log serum ferritin contributed significantly to RBP4 variance after controlling for BMI, age, and homeostasis model assessment value. Serum RBP4 concentration decreased after iron depletion in type 2 diabetic patients (percent mean difference -13.7 [95% CI -25.4 to -2.04]; P = 0.024). The iron donor lactoferrin led to increased dose-dependent adipose tissue release of RBP4 (2.4-fold, P = 0.005) and increased RBP4 expression, while apotransferrin and deferoxamine led to decreased RBP4 release.

CONCLUSIONS

The relationship between circulating RBP4 and iron stores, both cross-sectional and after iron depletion, and in vitro findings suggest that iron could play a role in the RBP4-insulin resistance relationship.

摘要

目的

视黄醇结合蛋白4(RBP4)与胰岛素抵抗之间关联的机制尚未完全明确。铁与维生素A状态(RBP4是其替代指标)之间的相互作用早已为人所知。我们推测,铁相关的胰岛素抵抗可能是RBP4导致胰岛素作用受损的原因。

研究设计与方法

在一组中年男性样本(n = 132)中评估血清铁蛋白、RBP4浓度和胰岛素抵抗,并进行一项独立的重复研究。还对2型糖尿病患者铁耗竭前后的血清RBP4进行了研究。最后,在体外评估铁对脂肪组织中RBP4释放的影响。

结果

在两项独立研究中均观察到循环RBP4与对数血清铁蛋白之间呈正相关(分别为r = 0.35和r = 0.61;P < 0.0001)。男性血清RBP4浓度高于女性,同时铁蛋白水平也升高。在预测血清RBP4的多元回归分析中,在控制体重指数、年龄和稳态模型评估值后,对数血清铁蛋白对RBP4变异有显著贡献。2型糖尿病患者铁耗竭后血清RBP4浓度降低(平均差异百分比 -13.7 [95%可信区间 -25.4至 -2.04];P = 0.024)。铁供体乳铁蛋白导致脂肪组织中RBP4的剂量依赖性释放增加(2.4倍,P = 0.005),且RBP4表达增加,而脱铁转铁蛋白和去铁胺导致RBP4释放减少。

结论

循环RBP4与铁储存之间的关系,无论是横断面研究还是铁耗竭后的研究,以及体外研究结果均表明,铁可能在RBP4 - 胰岛素抵抗关系中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55eb/2453621/413f5971daba/zdb0070853390001.jpg

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