Peripheral artery disease risk factors: A focus on lipoprotein(a)

Michele Dalla Vestra1, Elisabetta Grolla2, Giuliana Autiero1

  • 1Department of Internal Medicine, Ospedale dell'Angelo, 30174 Mestre-Venezia, Italy.

PubMed

Insights

High lipoprotein(a) levels are linked to coronary heart disease. This review examines its role in peripheral artery disease and carotid atherosclerosis, highlighting the need for future therapies.

Area of Science:

  • Cardiovascular Medicine
  • Atherosclerosis Research
  • Lipidology

Background:

  • A strong association exists between elevated lipoprotein(a) [Lp(a)] levels and coronary heart disease.
  • The role of Lp(a) in peripheral artery disease (PAD) and carotid atherosclerosis is less understood.
  • Current therapeutic options to lower Lp(a) are unavailable.

Purpose of the Study:

  • To review and synthesize the current evidence on the relationship between Lp(a), PAD, and carotid atherosclerosis.
  • To evaluate the significance of Lp(a) in the development, progression, and complications of atherosclerotic plaques in these vascular beds.
  • To establish Lp(a) as a potential target for managing residual vascular risk in PAD and carotid atherosclerosis patients.

Main Methods:

  • Systematic literature review of studies investigating Lp(a) in relation to PAD and carotid atherosclerosis.
  • Analysis of epidemiological, genetic, and clinical data.
  • Synthesis of findings to assess the impact of Lp(a) on atherosclerotic disease outcomes.

Main Results:

  • Evidence suggests a potential link between high Lp(a) and PAD/carotid atherosclerosis, though less conclusive than for coronary heart disease.
  • Lp(a) may contribute to plaque development, progression, and instability in peripheral and carotid arteries.
  • Understanding Lp(a)'s role is crucial for future risk stratification and therapeutic strategies.

Conclusions:

  • Lipoprotein(a) is an emerging, significant vascular risk factor for peripheral artery disease and carotid atherosclerosis.
  • Further research is needed to elucidate Lp(a)'s precise mechanisms in these conditions.
  • The development of Lp(a)-lowering therapies holds promise for reducing residual vascular risk in affected patients.

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