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Reduction of remnant lipoprotein cholesterol concentrations by cilostazol in patients with intermittent claudication

Tao Wang1, Marshall B Elam, William P Forbes

  • 1Otsuka America Pharmaceutical Inc., Rockville, MD, USA.

Atherosclerosis
|December 4, 2003
PubMed

Insights

Elevated remnant lipoproteins are common in intermittent claudication. Cilostazol treatment significantly reduces these atherogenic particles, potentially benefiting patients with peripheral arterial disease.

Area of Science:

  • Cardiovascular Medicine
  • Lipid Metabolism
  • Pharmacology

Background:

  • Intermittent claudication (IC) is linked to high triglyceride-rich lipoproteins and low high-density lipoproteins (HDL).
  • Remnant lipoproteins, a subset of triglyceride-rich lipoproteins, are implicated in atherosclerosis but their role in IC and response to cilostazol is unknown.

Purpose of the Study:

  • To investigate the association between remnant lipoproteins and peripheral arterial disease (PAD).
  • To evaluate the effect of cilostazol on remnant lipoprotein levels in patients with IC.

Main Methods:

  • Quantified plasma remnant lipoprotein-cholesterol (RLP-C) using a specific assay.
  • Compared RLP-C levels in IC patients (n=415) versus controls (n=874).
  • Assessed the impact of 6-month cilostazol treatment (100 mg b.i.d.) on RLP-C, triglycerides, and HDL cholesterol in IC patients (n=56) versus placebo (n=67).

Main Results:

  • IC patients exhibited significantly higher RLP-C (0.31 vs 0.24 mmol/l) and triglycerides, with lower HDL cholesterol compared to controls.
  • Cilostazol treatment reduced RLP-C by 20% (P < 0.05) and triglycerides (P < 0.01), while increasing HDL cholesterol (P < 0.001).
  • Placebo and pentoxifylline groups showed no significant changes in these lipid parameters.

Conclusions:

  • Remnant lipoprotein concentrations are significantly elevated in patients with intermittent claudication.
  • Cilostazol effectively reduces remnant lipoprotein levels in IC patients, suggesting a potential therapeutic benefit for symptomatic PAD.
Abstract

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