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Updated: Jul 5, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Recent clinical trials of pharmacologic cardiovascular interventions in patients with chronic kidney disease
M O Kaisar1, N M Isbel, D W Johnson
1Center for Kidney Disease Research, University of Queensland at Princess Alexandra Hospital, Brisbane, QLD, Australia.
Insights
Cardiovascular disease risk is high in end-stage kidney disease (ESKD). Reviewing trials shows interventions may not improve cardiac outcomes in CKD patients, questioning current guidelines.
Area of Science:
- Nephrology
- Cardiology
- Clinical Trials
Background:
- End-stage kidney disease (ESKD) significantly elevates cardiovascular mortality risk (10-20 fold).
- Most cardiovascular intervention trials exclude patients with chronic kidney disease (CKD).
Purpose of the Study:
- Critically review clinical trial evidence on cardiovascular risk factor interventions in CKD patients.
- Assess if cardiac outcomes in CKD are modified by interventions.
Main Methods:
- Review of published clinical trials on interventions including ESAs, statins, fibrates, folic acid, antioxidants, sevelamer, cinacalcet, ACE inhibitors, telmisartan, aspirin, and multidisciplinary clinics.
- Analysis of trial outcomes for cardiovascular events in CKD populations.
Main Results:
- No reviewed trials were conclusive regarding improved cardiac outcomes in CKD patients.
- Negative trial results challenge reliance on general population data for CKD cardiovascular guidelines.
Conclusions:
- Cardiovascular disease in CKD may be less responsive to interventions due to disease stage or different pathogenesis.
- Urgent need for large, well-designed, multi-center randomized controlled trials in this population.
Abstract:
End stage kidney disease (ESKD) is associated with a 10- to 20-fold increased risk of cardiovascular mortality compared with age- and sex-matched controls without CKD. In spite of this marked increase in risk, the vast majority of cardiovascular intervention clinical trials to date have specifically excluded subjects with CKD. The aim of this paper is to critically review the recently published clinical trial evidence that cardiac outcomes in CKD patients are modified by cardiovascular risk factor interventions, including erythropoiesis stimulating agent therapy (US Normal Hematocrit, CHOIR and CREATE trials), statins (PPP, 4D and ALERT), fibrates (VA-HIT), folic acid (ASFAST, US folic acid trial, HOST), anti-oxidative stress therapy (SPACE, HOPE and ATIC), N-acetylcysteine, sevelamer (D-COR), cinacalcet (Cunningham meta-analysis), carvedilol, angiotensin converting enzyme inhibitor (FOSIDIAL), telmisartan, aspirin (HOT study re-analysis) and multidisciplinary multiple cardiovascular risk factor intervention clinics (LANDMARK). Although none of these studies could be considered conclusive, the negative trials to date should raise significant concerns about the heavy reliance of current clinical practice guidelines on extrapolation of findings from cardiovascular intervention trials in the general population. It may be that cardiovascular disease in dialysis populations is less amenable to intervention, either because of the advanced stage of CKD or because the pathogenesis of cardiovascular disease in CKD patients is different to that in the general population. Further large, well-conducted, multi-centre randomised controlled trials in this area are urgently required.
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