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Updated: Jul 11, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cardiovascular disease in patients with chronic kidney disease. A clinical review
M Kaisar1, N Isbel, D W Johnson
1Centre for Kidney Disease Research, University of Queensland at Princess, Alexandra Hospital, Brisbane, QLD Australia.
Insights
Cardiovascular disease (CVD) is a major cause of death in chronic kidney disease (CKD) patients, with limited interventional trials. More research is needed to understand and treat CVD in this vulnerable population.
Area of Science:
- Nephrology
- Cardiology
- Clinical Trials
Background:
- Cardiovascular disease (CVD) is the leading cause of premature death in patients with chronic kidney disease (CKD).
- CKD patients face a 10-20 times higher risk of cardiac death compared to the general population.
- Both traditional and renal-specific factors contribute to the elevated CVD burden in CKD.
Purpose of the Study:
- To review the current state of interventional cardiovascular randomized controlled trials (RCTs) in the CKD population.
- To highlight the lack of robust clinical evidence for CVD management in CKD.
- To emphasize the need for further large-scale, well-designed trials.
Main Methods:
- Review of existing literature on cardiovascular risk factors and interventions in CKD.
- Analysis of findings from recent RCTs addressing dyslipidemia, cardiomyopathy, anemia, hyperhomocysteinemia, bone mineral metabolism, and oxidative stress.
- Assessment of the limitations and exclusions of CKD patients from mainstream cardiovascular trials.
Main Results:
- Despite numerous trials on various risk factors, level 1 clinical evidence for CVD interventions in CKD remains significantly lacking.
- Many trials yielded negative findings, suggesting that interventions effective in non-CKD populations may not translate.
- CKD patients are often excluded from major cardiovascular trials, limiting generalizability.
Conclusions:
- There is an urgent need for large, well-designed cardiovascular RCTs specifically in the CKD population.
- Extrapolating findings from non-CKD patients to those with kidney disease may be dangerous.
- Further research is critical to establish effective CVD prevention and treatment strategies for individuals with CKD.
Abstract:
Cardiovascular disease (CVD) remains the most common cause of premature death in the chronic kidney disease (CKD) population. Individuals with CKD are at 10-20 times greater risk of cardiac death than controls without CKD, despite stratification for age, race, sex and diabetes. Heightened CVD mortality begins with mild kidney disease and rises further with more advanced kidney disease. Traditional risk factors account for up to 50% of cardiovascular disease in CKD, whilst renal specific markers, including anemia, disordered bone mineral metabolism and oxidative stress, also likely contribute to the total cardiovascular burden in CKD. Despite the increased mortality, there has been a dearth of interventional cardiovascular randomized controlled trials (RCTs) in the CKD population. Furthermore, many patients with kidney disease have been excluded from the majority of mainstream cardiovascular interventional trials. While recently published RCTs on traditional and non-traditional risk factors including dyslipidemia (PPP, 4D and ALERT, VA-HIT), cardiomyopathy (FOSIDIAL, telmisartan, carvedilol), anemia (US Normal Hematocrit, CHOIR and CREATE trials), hyperhomocystenemia (ASFAST, US folic acid trial, HOST), disordered bone mineral metabolism (Cunningham meta-analysis, DCOR), oxidative stress therapy (SPACE, HOPE and ATIC, N-acetylcysteine) and multidisciplinary multiple cardiovascular risk factor intervention clinics (LANDMARK) have added to the available pool of clinical data, level 1 clinical evidence remains significantly lacking. The negative findings in many of these trials highlight the potential dangers of extrapolating findings from non kidney disease patients to those with CKD. Further large, well-designed trials are urgently required to address this issue.
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