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.