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These studies suggest sevelamer is used to manage hyperphosphatemia in chronic kidney disease patients, reduce cardiovascular calcification, and improve inflammation and lipid profiles, with potential survival benefits and fewer risks of hypercalcemia compared to calcium-based binders.
20 papers analyzed
Sevelamer is a non-absorbed polymer used primarily to manage hyperphosphatemia in patients with chronic kidney disease (CKD), particularly those on dialysis. It functions by binding dietary phosphate in the gastrointestinal tract, thereby reducing serum phosphate levels without increasing calcium levels.
Sevelamer is effective in controlling serum phosphate levels in CKD patients. Studies have shown that while calcium-based phosphate binders (CBBs) may slightly outperform sevelamer in lowering serum phosphate, sevelamer still provides significant phosphate reduction without the risk of hypercalcemia . This makes it a safer alternative for patients at risk of elevated calcium levels.
One of the key advantages of sevelamer over CBBs is its ability to manage hyperphosphatemia without causing hypercalcemia. Multiple studies have demonstrated that sevelamer is associated with significantly lower serum calcium levels and a reduced risk of hypercalcemia compared to CBBs . This is particularly beneficial for patients who are prone to calcium-related complications.
Sevelamer has been shown to attenuate the progression of vascular calcification, a common and severe complication in CKD patients. Research indicates that sevelamer significantly reduces coronary artery and aortic calcification compared to calcium-based binders . This effect is crucial in reducing cardiovascular morbidity and mortality in this patient population.
Sevelamer also exhibits anti-inflammatory and anti-atherogenic properties. It has been found to lower levels of inflammatory markers such as C-reactive protein (CRP) and improve lipid profiles by reducing total cholesterol and low-density lipoprotein (LDL) cholesterol. These changes contribute to its potential in reducing cardiovascular risk in hemodialysis patients.
Short-term treatment with sevelamer has been associated with improvements in endothelial function, as evidenced by increased serum fetuin-A concentrations and enhanced flow-mediated dilation (FMD) in CKD patients. These improvements suggest a beneficial effect on vascular health beyond phosphate binding.
Several meta-analyses and systematic reviews have compared sevelamer with calcium-based binders. These studies consistently show that sevelamer is associated with lower all-cause mortality and a reduced risk of hypercalcemia, although it may not significantly differ in terms of overall phosphate reduction . Additionally, sevelamer's ability to slow the progression of vascular calcification and improve lipid profiles further supports its use in managing hyperphosphatemia in CKD patients.
While sevelamer is generally well-tolerated, it may be associated with gastrointestinal adverse effects. However, these effects are not significantly different from those observed with calcium-based binders . The overall safety profile of sevelamer makes it a viable option for long-term management of hyperphosphatemia in CKD patients.
Sevelamer is a valuable therapeutic option for managing hyperphosphatemia in CKD patients, particularly those on dialysis. Its ability to control serum phosphate without causing hypercalcemia, along with its cardiovascular benefits, makes it a preferred choice over calcium-based phosphate binders. The reduction in vascular calcification, improvement in lipid profiles, and anti-inflammatory effects further enhance its clinical utility in this patient population.
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