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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.
Abstract:
Cardiovascular disease (CVD) accounts for more than 50% of deaths among patients with end-stage kidney disease (ESKD). Approximately 40-50% of ESKD patients have clinically significant coronary artery disease (CAD) due to atherosclerosis which accounts for a significant proportion of CVD risk. However, other CVD pathologies including myocardial fibrosis, vascular calcification and arterial stiffening play important contributory roles. The pathophysiology of CAD in ESKD is distinct from the general population. ESKD patients is typically have diffuse multi-vessel involvement with increased calcification that involves both intimal and medial layers of the arterial wall. There is a complex interplay between an increased burden of traditional Framingham risk factors and exposure to non-traditional risk factors including chronic inflammation and dialysis per se. Established treatments for CAD risk factors including cholesterol lowering with statin therapy have attenuated effects and ESKD patients also have worse outcomes after revascularisation. Recent trials such as the Canakinumab Anti-Inflammatory Thrombosis Outcomes Study (CANTOS) have established that direct modulation of inflammation improves CVD outcomes in the general population, which may prove to be a potential attractive therapeutic target in ESKD patients. Multiple retrospective observational studies comparing mortality outcomes between haemodialysis (HD) and peritoneal dialysis (PD) patients have been inconclusive. Randomised trials on this issue of clinical equipoise are clearly warranted but are unlikely to be feasible. Screening for stable CAD in asymptomatic ESKD patients remains a clinical dilemma which is unique to chronic dialysis patients being assessed for kidney transplantation. This has become particularly relevant in light of the recent ISCHEMIA-CKD trial which demonstrated no difference between optimal medical therapy and revascularisation upon CVD outcomes or mortality. The optimal strategy for screening is currently being investigated in the ongoing large international multi-centre CARSK trial. Here we discuss the pathophysiology, risk modification, treatment, screening and future directions of CAD in ESKD.
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