Related Experiment Video
Updated: Aug 8, 2026

Hydra, a Computer-Based Platform for Aiding Clinicians in Cardiovascular Analysis and Diagnosis
Published on: September 26, 2018
Hyperphosphataemia as a cardiovascular risk factor -- how to manage the problem
Jorge B Cannata-Andía1, Minerva Rodríguez-García
1Bone and Mineral Research Unit, Instituto Reina Sofía de Investigación, Hospital Central de Asturias, Universidad de Oviedo, Oviedo, Spain. metoseo@hca.es
Insights
Managing high phosphate levels (hyperphosphatemia) in chronic kidney disease (CKD) is crucial for cardiovascular health. Controlling serum phosphate and calcium reduces vascular calcification and mortality risk in CKD patients.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Biochemistry
Background:
- Hyperphosphatemia is a significant cardiovascular risk factor in chronic kidney disease (CKD).
- Elevated phosphate levels contribute to vascular calcification through secondary hyperparathyroidism and direct calcium phosphate deposition.
- High phosphate levels are linked to increased mortality in CKD patients.
Purpose of the Study:
- To outline strategies for managing hyperphosphatemia in CKD patients.
- To emphasize the importance of controlling serum phosphate and calcium levels to mitigate cardiovascular risks.
- To discuss the role of diet, phosphate binders, and dialysis in phosphate management.
Main Methods:
- A multi-faceted approach including dietary modification, appropriate use of phosphate binders, and optimized dialysis.
- Maintaining serum phosphate <5 mg/dL and serum calcium <10 mg/dL to keep the calcium x phosphate product ≤50 mg²/dL².
- Utilizing non-calcium, non-aluminum phosphate binders like sevelamer hydrochloride.
Main Results:
- Effective phosphate control reduces the risk of vascular, valvular, and extraskeletal calcification.
- Sevelamer hydrochloride demonstrates efficacy and potential benefits on lipid profiles.
- Continuous ambulatory peritoneal dialysis may offer better phosphate control compared to hemodialysis.
Conclusions:
- A comprehensive management strategy is essential for controlling hyperphosphatemia in CKD.
- Optimizing dialysis parameters (duration and frequency) is crucial for phosphate removal.
- Careful selection and dosing of phosphate binders, particularly non-calcium-based ones, are vital.
Abstract:
Hyperphosphataemia is a frequent and important cardiovascular risk factor in patients with chronic kidney disease (CKD). High phosphate levels may influence vascular calcifications by two separate mechanisms: by worsening secondary hyperparathyroidism, which in turn facilitates calcification, and by promoting calcium phosphate deposition in pre-formed endothelial plaques and in the arterial wall. Recent studies have shown that hyperphosphataemia induces the proliferation and differentiation of endothelial vascular cells into osteoblast-like cells, promoting vascular calcification. High phosphate levels also increase the risk of mortality in patients with CKD. To reduce the negative impact of high phosphate, serum phosphate levels should be <5 mg/dl and serum calcium <10 mg/dl. This allows the calcium x phosphate product to be maintained at < or =50 mg(2)/dl(2), reducing the risk of vascular, valvular, and extraskeletal calcification. A multiple-factor approach can be used to reduce serum phosphate: (i). decrease bone resorption by maintaining adequate serum parathyroid hormone levels; (ii). reduce phosphorous intake in the diet, (iii). use phosphate binders efficiently; and (iv). avoid under-dialysis. The patient's diet should be high in nutrition but with the lowest possible phosphorous content. Doses of phosphate binders should be tailored to individual dietary habits and must be taken during meals in a dose proportional to the phosphorous content of the meal. Because of the risk of increased extraskeletal calcification, calcium-containing phosphate-binder intake should not exceed 2-3 g/day. Sevelamer hydrochloride, a non-calcium and non-aluminium phosphate binder with a potency similar to that of calcium salts has shown beneficial effects on lipid profiles. Better control of serum phosphate is achieved in patients on continuous ambulatory peritoneal dialysis than in those on haemodialysis. Removal of phosphate is directly correlated with duration and frequency of dialysis sessions. Thus, it is advisable not to reduce the duration of dialysis sessions to <4 h three times per week.
More Related Videos
Related Concept Videos
Hypertension and Regulation of Blood Pressure
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Coronary Artery Disease IV: Preventive Measures
Atherosclerosis III: Management
Peripheral Artery Disease III: Interprofessional Care
Chronic Kidney Disease II: Clinical Manifestations

