Apolipoprotein B-containing lipoproteins and atherosclerotic cardiovascular disease

Michael D Shapiro1, Sergio Fazio1

  • 1Center for Preventive Cardiology, Knight Cardiovascular Institute, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR, 97239, USA.

F1000Research
|March 17, 2017
PubMed

Insights

Apolipoprotein B (apoB)-containing lipoproteins are key drivers of atherosclerotic cardiovascular disease. This review covers their role in atherosclerosis, alongside other factors and foam cell biology.

Area of Science:

  • Cardiovascular Science
  • Lipid Metabolism
  • Atherosclerosis Research

Background:

  • Apolipoprotein B (apoB)-containing lipoproteins are established as major causal agents in atherosclerotic cardiovascular disease.
  • Converging evidence highlights low-density lipoprotein (LDL) and related particles as central to atherosclerosis development.

Purpose of the Study:

  • To review the critical role of atherogenic apoB-containing lipoproteins in cardiovascular disease.
  • To discuss other contributing humoral and parietal factors in arterial degeneration.
  • To briefly review foam cell biology and high-density lipoprotein (HDL) interactions, including cholesterol efflux.

Main Methods:

  • Literature review of fundamental research on lipoprotein metabolism and atherosclerosis.
  • Synthesis of evidence from multiple orthogonal lines of research.
  • Review of cellular and molecular mechanisms involved in atherogenesis.

Main Results:

  • Atherogenic apoB-lipoproteins are principal etiological agents in atherosclerosis.
  • Arterial degeneration requires the interplay of lipoproteins with other humoral and parietal factors.
  • Foam cell formation and HDL-mediated cholesterol efflux are integral to the disease process.

Conclusions:

  • Atherogenic apoB-lipoproteins are indispensable in the pathogenesis of cardiovascular disease.
  • Understanding these lipoproteins and associated factors is crucial for developing effective therapies.
  • Further research into foam cell dynamics and HDL function can offer new therapeutic targets.

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