The Controversies of Coronary Artery Disease in End-Stage Kidney Disease Patients: A Narrative Review

Daniel Hirsch1,2, Brandon Lau2, Virag Kushwaha2,3

  • 1Department of Nephrology, Prince of Wales Hospital, Randwick, NSW 2031, Australia.

Insights

Cardiovascular disease (CVD) is a major cause of death in end-stage kidney disease (ESKD) patients, often involving complex atherosclerosis. Understanding unique pathophysiology and exploring novel treatments like inflammation modulation are crucial for improving outcomes.

Area of Science:

  • Nephrology and Cardiovascular Medicine
  • Renal disease and Atherosclerosis research
  • Chronic kidney disease and Cardiac complications

Background:

  • Cardiovascular disease (CVD) causes over 50% of deaths in end-stage kidney disease (ESKD) patients.
  • ESKD patients exhibit unique coronary artery disease (CAD) pathophysiology, including diffuse multi-vessel involvement and extensive arterial calcification.
  • Traditional risk factors are compounded by non-traditional factors like chronic inflammation and dialysis itself.

Purpose of the Study:

  • To review the distinct pathophysiology of CAD in ESKD patients.
  • To discuss risk modification strategies, treatment challenges, and screening dilemmas for CAD in ESKD.
  • To explore future directions and potential therapeutic targets, such as inflammation modulation.

Main Methods:

  • Review of existing literature on cardiovascular disease in end-stage kidney disease.
  • Analysis of pathophysiology, risk factors, and treatment outcomes specific to ESKD patients.
  • Discussion of inconclusive evidence from observational studies and the need for randomized trials.

Main Results:

  • CAD in ESKD differs significantly from the general population, with increased calcification and diffuse disease.
  • Standard CAD treatments, like statins, show attenuated effects, and revascularization outcomes are often worse in ESKD.
  • Inflammation modulation is a potential therapeutic avenue, while screening strategies and dialysis modality comparisons remain debated.

Conclusions:

  • The unique pathophysiology of CAD in ESKD necessitates tailored approaches to risk management and treatment.
  • Further research is needed to clarify the optimal screening strategies and the role of different dialysis modalities.
  • Targeting inflammation presents a promising, yet unproven, therapeutic strategy for reducing CVD burden in ESKD.

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