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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Management of dyslipidemia after coronary artery bypass grafting
1Oklahoma Medical Research Foundation, Oklahoma City 73104, USA. alaupovicp@omrf.ouhsc.edu
Insights
Abnormalities in plasma lipoproteins significantly accelerate atherosclerosis in vein grafts after bypass surgery. Early, aggressive pharmacological treatment of dyslipoproteinemias is crucial for graft survival.
Area of Science:
- Cardiovascular Science
- Lipid Metabolism
- Vascular Biology
Background:
- Saphenous vein grafts are susceptible to atherosclerotic attrition after coronary artery bypass grafting.
- Plasma lipoprotein system abnormalities are a major risk factor for this graft degeneration.
Purpose of the Study:
- To analyze the role of different lipoprotein particles in the progression of atherosclerosis in vein grafts.
- To evaluate the impact of dyslipoproteinemia treatment on graft outcomes.
Main Methods:
- Review of serial angiographic studies in post-coronary artery bypass grafting patients.
- Analysis of data from intervention trials targeting lipoprotein abnormalities.
Main Results:
- Cholesterol-rich low-density lipoprotein (LDL) and lipoprotein B particles contribute to atherosclerotic lesion progression.
- Triglyceride-rich very low-density lipoprotein and intermediate-density lipoprotein particles also exhibit atherogenic capacity.
- High-density lipoprotein 3 particles may offer a protective effect against atherosclerosis.
Conclusions:
- Dyslipoproteinemias are a critical risk factor for saphenous vein graft atherosclerosis.
- Early and aggressive pharmacological treatment of dyslipoproteinemias is essential for preserving vein graft function.
- Targeting specific lipoprotein abnormalities can delay or prevent graft attrition.
Abstract:
The results of serial angiographic studies and intervention trials in patients after coronary artery bypass artery grafting have provided ample evidence that abnormalities of the plasma lipoprotein system are one of the most significant risk factors for a rapid atherosclerotic attrition of saphenous vein grafts. In addition to confirming the well recognized role and contribution of cholesterol-rich LDL or lipoprotein B particles to the progression of atherosclerotic lesions, intervention trials have also provided strong evidence for the atherogenic capacity of some intact and partly delipidized triglyceride-rich very low density lipoprotein and intermediate density lipoprotein (lipoprotein B complex) particles, and the protective effect of some (high density lipoprotein 3) but not all high density lipoprotein particles. Most importantly, those studies have emphasized the need for an early, aggressive treatment of dyslipoproteinemias with pharmacological agents as the most efficient therapeutic approach to delaying, if not preventing, the detrimental effect of atherosclerosis on saphenous vein grafts.
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