Review
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World J Diabetes. Sep 15, 2010; 1(4): 116-128
Published online Sep 15, 2010. doi: 10.4239/wjd.v1.i4.116
Pharmacological effects of lipid-lowering drugs on circulating adipokines
Desiree Wanders, Eric P Plaisance, Robert L Judd
Desiree Wanders, Robert L Judd, Department of Anatomy, Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, Auburn, AL 36849, United States
Eric P Plaisance, Laboratory of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, LA 70808, United States
Author contributions: Wanders D, Plaisance EP and Judd RL contributed equally to this paper.
Supported by Boshell Diabetes and Metabolic Diseases Research Program
Correspondence to: Robert L Judd, PhD, Department of Anatomy, Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, 219 Greene Hall, Auburn, AL 36849, United States. juddrob@auburn.edu
Telephone: +1-334-844-5416 Fax: +1-334-844-5388
Received: May 4, 2010
Revised: June 29, 2010
Accepted: July 6, 2010
Published online: September 15, 2010
Abstract

The cardioprotective effects of lipid-lowering drugs have been primarily attributed to their effects on blood lipid metabolism. However, emerging evidence indicates that lipid-lowering drugs also modulate the synthesis and secretion of adipose tissue-secreted proteins referred to as adipokines. Adipokines influence energy homeostasis and metabolism and have also been shown to modulate the vascular inflammatory cascade. The purpose of this review will be to examine the reported effects of commonly used lipid-lowering drugs (statins, fibrates, niacin and omega-3-fatty acids) on the circulating concentrations of leptin, adiponectin, tumor necrosis-factor-α (TNF-α), Retinol binding protein 4 (RBP4) and resistin. Overall, the lipid-lowering drugs reviewed have minimal effects on leptin and resistin concentrations.Conversely, circulating adiponectin concentrations are consistently increased by each lipid-lowering drug reviewed with the greatest effects produced by niacin. Studies that have examined the effects of statins, niacin and omega-3-fatty acids on TNF-α demonstrate that these agents have little effect on circulating TNF-α concentrations. Niacin and fibrates appear to lower RBP4 but not resistin concentrations. The results of the available studies suggest that a strong relationship exists between pharmacological reductions in blood lipids and adiponectin that is not obvious for other adipokines reviewed.

Keywords: Statins, Fibrates, Niacin, Omega-3 fatty acids, Adipokines, Leptin, Adiponectin, Cardiovascular disease, Hyperlipidemia