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Updated: Apr 21, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cardiovascular disease and its relationship with chronic kidney disease
1Graduate School, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China. mwlj521@163.com.
Insights
Cardiovascular disease (CVD) and chronic kidney disease (CKD) are linked, with CKD increasing CVD mortality. Understanding nontraditional risk factors and novel therapies is crucial for managing these interconnected conditions.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Cardiovascular disease (CVD) is the leading cause of death, often linked to cardiometabolic risk and chronic kidney disease (CKD).
- CKD significantly elevates mortality risk from CVD, particularly in end-stage renal disease (ESRD) patients.
- Traditional CVD risk factors and treatments are less effective in CKD patients, highlighting the need for understanding nontraditional factors.
Purpose of the Study:
- To review the complex biological, pathological, and clinical interrelationships between CVD and CKD.
- To explore nontraditional risk factors contributing to the high CVD burden in CKD patients.
- To discuss current and emerging therapeutic strategies for managing comorbid CVD and CKD.
Main Methods:
- Literature review of studies examining the links between CKD and CVD.
- Analysis of traditional and nontraditional risk factors for CVD in CKD populations.
- Synthesis of information on therapeutic interventions for combined CVD and CKD management.
Main Results:
- Disturbed mineral and vitamin D metabolism, including Fibroblast Growth Factor 23 (FGF23), contribute to vascular calcification and CVD risk in CKD.
- Uremic toxins like indoxyl sulfate and p-cresyl sulfate exacerbate renal dysfunction.
- Acute Kidney Injury (AKI) is strongly associated with CVD progression.
Conclusions:
- Effective CVD prevention in CKD requires addressing blood pressure, dyslipidemia, diabetes, proteinuria, anemia, mineral metabolism, and lifestyle factors.
- Emerging therapies targeting colonic microbiota offer new avenues for early CKD intervention.
- Comprehensive management strategies integrating CVD and CKD care are essential for improving patient outcomes.
Abstract:
Cardiovascular disease (CVD), the leading cause of death, is mostly precipitated by cardiometabolic risk and chronic kidney disease (CKD). CVD and kidney disease are closely interrelated and disease of one organ cause dysfunction of the other, ultimately leading to the failure of both organs. Patients with end-stage renal disease (ESRD) are at much higher risk of mortality due to CVD. Traditional CVD risk factors viz., hypertension, hyperlipidemia, and diabetes do not account for the high cardiovascular risk in CKD patients and also standard clinical interventions for managing CVD that are successful in the general population, are ineffective to lower the death rate in CKD patients. Nontraditional factors, related to disturbed mineral and vitamin D metabolism were able to provide some explanation in terms of vascular calcification, for the increased risk of CVD in CKD. Fibroblast Growth Factor 23, a bone-derived hormone that regulates vitamin D synthesis in renal proximal tubules and renal phosphate reabsorption, has been suggested to be the missing link between CKD and CVD. Acute Kidney Injury (AKI) is strongly related to the progress of CVD and its early diagnosis and treatment has significant positive effect on the outcomes of CVD in the affected patients. Besides this, non-dialysable protein-bound uraemic toxins such as indoxyl sulfate and p-cresyl sulfate, produced by colonic microbes from dietary amino acids, appear to cause renal dysfunction. Thus, therapeutic approaches targeting colonic microbiota, have led to new prospects in early intervention for CKD patients. Intervention targets for preventing CVD events in CKD patients ideally should include control of blood pressure and dyslipidemia, diabetes mellitus, lowering proteinuria, correction of anemia, management of mineral metabolism abnormalities and life style changes including smoking cessation, decreased consumption of salt, and achievement of normal body mass index. Use of β-blockers, renin-angiotensin blockers, diuretics, statins, and aspirin are helpful in the early stages of CKD. In this review, we will address the biological, pathological and clinical relationship between CVD and CKD and their therapeutic management.
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