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Serum levels of the adipokine RBP-4 in relation to renal function

  1. Michaela Ziegelmeier, MS1,
  2. Anette Bachmann, MD1,
  3. Jeannette Seeger, MS1,
  4. Ulrike Lossner, BS1,
  5. Jürgen Kratzsch, PhD2,
  6. Matthias Blüher, MD1,,3,
  7. Michael Stumvoll, MD1,,3 and
  8. Mathias Fasshauer, MD (mathias.fasshauer{at}medizin.uni-leipzig.de)1,,3
  1. 1 University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
  2. 2 University of Leipzig, Institute of Laboratory Medicine, 04103 Leipzig, Germany
  3. 3 Interdisciplinary Center for Clinical Research (IZKF) Leipzig, 04103 Leipzig, Germany

    Abstract

    Objective: RBP-4 was recently identified as an adipokine inducing insulin resistance. In the current study, we investigated RBP-4 serum levels in diabetic and non-diabetic patients on chronic hemodialysis (CD) as compared to controls with a glomerular filtration rate above 50 ml/min. The majority of the diabetic subjects used oral hypoglycemic agents or insulin.

    Research Design and Methods: RBP-4 was determined by ELISA in control (n=59) and CD (n=58) patients and correlated to clinical and biochemical measures of renal function, glucose and lipid metabolism, as well as inflammation, in both groups.

    Results: Mean serum RBP-4 levels were almost 4-fold higher in CD patients (102 ± 30 mg/l) as compared to controls (28 ± 8 mg/l). Furthermore, serum creatinine independently predicted RBP-4 concentrations in multiple regression analyses in both, control subjects and CD patients. In addition, CRP and systolic blood pressure independently and negatively correlated with RBP-4 serum concentrations in CD patients but not controls. In contrast, markers of glucose and lipid metabolism were not independently related to serum RBP-4 in control subjects or CD patients.

    Conclusions: We show that markers of renal function are independently related to serum RBP-4 levels.

    Footnotes

      • Received February 9, 2007.
      • Accepted July 9, 2007.

    This Article

    1. Diabetes Care July 13, 2007
    1. All Versions of this Article:
      1. dc07-0275v1
      2. 30/10/2588 most recent
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