Key result
MBX-8025 alone and combined with atorvastatin significantly reduced apolipoprotein B-100 by 20-38%, LDL by 18-43%, and triglycerides by 26-30% compared to placebo (P<0.05).
Why the study?
Does MBX-8025 alone or in combination with atorvastatin improve lipid and metabolic parameters in overweight patients with mixed dyslipidemia?
RCT (n=181)
double-blind
randomized
Yes
Does MBX-8025 alone or in combination with atorvastatin improve lipid and metabolic parameters in overweight patients with mixed dyslipidemia?
p-value: p=<0.05
The novel PPAR-δ agonist MBX-8025 significantly improved multiple proatherogenic lipid and metabolic parameters in overweight patients with mixed dyslipidemia, both alone and when added to atorvastatin.
MBX-8025 may add a novel mechanism for mixed dyslipidemia; extends PPAR-δ agonism as adjunctive lipid-lowering therapy.
CONTEXT: Preclinical and clinical studies suggest that peroxisome proliferator-activated receptor (PPAR)-δ agonists favorably affect multiple metabolic parameters that are otherwise proatherogenic, many that are not optimally managed with statins alone. OBJECTIVE: The aim of this study was to evaluate the effects of MBX-8025 (a novel PPAR-δ agonist) on lipid and other metabolic parameters associated with increased atherosclerotic risk, administered alone and in combination with atorvastatin. DESIGN AND SETTING: This was a randomized, double-blind, placebo-controlled, parallel group proof-of-concept study conducted at 30 U.S. research sites. PARTICIPANTS: This study evaluated 181 overweight men and women with mixed dyslipidemia. INTERVENTION(S): Subjects were administered once daily placebo, atorvastatin 20 mg, or MBX-8025 at 50 or 100 mg alone or combined with atorvastatin for 8 wk. MAIN OUTCOME MEASURES: The main efficacy measures included change from baseline in apolipoprotein B-100, lipid levels, high-sensitivity C-reactive protein, and additional metabolic parameters, as well as the effect on the metabolic syndrome and LDL particle size. RESULTS: Compared to placebo, MBX-8025 alone and in combination with atorvastatin significantly (P < 0.05) reduced apolipoprotein B-100 20-38%, LDL 18-43%, triglycerides 26-30%, non-high-density lipoprotein cholesterol 18-41%, free fatty acids 16-28%, and high-sensitivity C-reactive protein 43-72%; it raised high-density lipoprotein cholesterol 1-12% and also reduced the number of patients with the metabolic syndrome and a preponderance of small LDL particles. MBX-8025 was safe and generally well-tolerated. MBX-8025 also reduced liver enzyme levels. CONCLUSION: MBX-8025, a novel PPAR-δ agonist, favorably affected multiple metabolic parameters with and without atorvastatin. A more complete understanding of MBX-8025 requires a larger future study.
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Bays et al. (2011) conducted an RCT in mixed dyslipidemia (n=181). MBX-8025 vs. placebo was evaluated on change from baseline in apolipoprotein B-100, lipid levels, high-sensitivity C-reactive protein, and additional metabolic parameters (p=<0.05). MBX-8025 alone and combined with atorvastatin significantly reduced apolipoprotein B-100 by 20-38%, LDL by 18-43%, and triglycerides by 26-30% compared to placebo (P<0.05).
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