Effects of the PPAR-δ agonist MBX-8025 on atherogenic dyslipidemia

Abstract 

Objective

Determine the effects of treatment with a selective PPAR-δ agonist±statin on plasma lipoprotein subfractions in dyslipidemic individuals.

Methods

Ion mobility analysis was used to measure plasma concentrations of subfractions of the full spectrum of lipoprotein particles in 166 overweight or obese dyslipidemic individuals treated with the PPAR-δ agonist MBX-8025 (50 and 100mg/d)±atorvastatin (20mg/d) in an 8-week randomized parallel arm double blind placebo controlled trial.

Results

MBX-8025 at both doses resulted in reductions of small plus very small LDL particles and increased levels of large LDL, with a concomitant reduction in large VLDL, and an increase in LDL peak diameter. This translated to reversal of the small dense LDL phenotype (LDL pattern B) in ∼90% of the participants. Modest increases in HDL particles were confined to the smaller HDL fractions. Atorvastatin monotherapy resulted in reductions in particles across the VLDL–IDL–LDL spectrum, with a significantly smaller reduction in small and very small LDL vs. MBX-8025 100mg/d (−24.5±5.3% vs. −47.8±4.9%), and, in combination with MBX-8025, a reversal of the increase in large LDL.

Conclusion

PPAR-δ and statin therapies have complementary effects in improving lipoprotein subfractions associated with atherogenic dyslipidemia.

Keywords: Peroxisome proliferator activated receptor delta, Lipoprotein subfractions, VLDL, LDL, HDL, Triglyceride, Small dense LDL