Effect of weight loss on LDL and HDL kinetics in the metabolic syndrome: Associations with changes in plasma retinol-binding protein-4 and adiponectin levels

  1. Theodore W.K. Ng, BSc (gerald.watts{at}uwa.edu.au)1,
  2. Gerald F. Watts, MD, DSc (gerald.watts{at}uwa.edu.au)1,
  3. P Hugh R. Barrett, PhD1,
  4. Kerry-Anne Rye, PhD2,,3 and
  5. Dick C. Chan, PhD1
  1. 1School of Medicine and Pharmacology, Metabolic Research Centre, University of Western Australia
  2. 2Lipid Research Group, The Heart Research Institute, and
  3. 3Department of Medicine, University of Sydney, Sydney, NSW, Australia

    Abstract

    Objectives: To examine the effect of weight loss on LDL and HDL kinetics and plasma retinol-binding protein-4 (RBP-4) and adiponectin levels in men with the metabolic syndrome (MetS).

    Research design and Methods: LDL-apoB-100 and HDL-apoA-I kinetics were studied in 35 obese men with the MetS at the start and end of a 16-week intervention trial of a hypocaloric, low-fat diet (n=20) versus a weight maintenance diet (n=15), using a stable isotope technique and multi-compartmental modelling.

    Results: The low-fat diet achieved significant reduction (P<0.01) in BMI, abdominal fat compartments and HOMA score compared with weight maintenance. This was associated with a significant increase in adiponectin and a fall in plasma RBP-4, triglycerides, LDL-cholesterol, and LDL-apoB concentration (P<0.05). Weight loss significantly increased the catabolism of LDL-apoB (+27%, P<0.05), but did not affect production; it also decreased both the catabolic (-13%) and production (-13%) rates of HDL-apoA-I (P<0.05), thereby not altering plasma HDL-apoA-I or HDL-cholesterol concentrations. VLDL-apoB production fell significantly with weight loss (P<0.05). The increase in LDL catabolism was inversely correlated with the fall in RBP-4 (r=-0.54, P<0.05), and the decrease in HDL catabolism with the rise in adiponectin (r= -0.56, P<0.01).

    Conclusion: In obese men with MetS, weight loss with a low-fat diet decreases plasma LDL-apoB concentration by increasing the catabolism of LDL-apoB; weight loss also delays the catabolism of HDL-apoA-I with a concomitant reduction in the secretion of HDL-apoA-I. These effects of weight loss could partly involve changes in RBP-4 and adiponectin levels.

    Footnotes

      • Received April 20, 2007.
      • Accepted July 25, 2007.