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

Summary 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...

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Veröffentlicht in:Wiener medizinische Wochenschrift 2011-11, Vol.161 (21-22), p.505-510
Hauptverfasser: Mostafaie, Nazanin, Sebesta, Christian, Zehetmayer, Sonja, Jungwirth, Susanne, Huber, Klaus R., Hinterberger, Margareta, Leitha, Thomas, Hofman, Jörg, Hejtman, Milos, Schrattbauer, Karl, Krugluger, Walter, Tragl, Karl-Heinz, Fischer, Peter
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Sprache:eng
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Zusammenfassung:Summary 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
ISSN:0043-5341
1563-258X
DOI:10.1007/s10354-011-0885-7