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Published on: May 31, 2016
Progression of cardiac valve calcification and decline of renal function in CKD patients
Luca Di Lullo1, Fulvio Floccari, Alberto Santoboni
1Department of Nephrology and Dialysis, L Parodi Delfino Hospital, Colleferro, Italy.
Insights
Sevelamer, a phosphate binder, significantly reduced cardiac valve calcification and slowed kidney function decline in chronic kidney disease patients. It also lowered FGF-23, CRP, and phosphorus excretion.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Limited data exists on non-calcium-containing phosphate binders' effects on cardiac valve calcification and kidney function in chronic kidney disease (CKD) patients.
- This study investigated sevelamer's efficacy in patients with stage 3-4 CKD and valve calcification.
Purpose of the Study:
- To evaluate the impact of sevelamer hydrochloride on cardiac valve calcification progression.
- To assess the effect of sevelamer on renal function decline in CKD patients.
- To analyze changes in parathyroid hormone, FGF-23, CRP, and urinary phosphorus excretion.
Main Methods:
- A prospective observational study involving 170 outpatients with stage 3-4 CKD and mitral or aortic valve calcification.
- Patients received sevelamer hydrochloride (1,600 mg/day) for one year.
- Cardiac valve calcification assessed by echocardiography; renal function by estimated glomerular filtration rate (eGFR); serum and urinary markers were assayed.
Main Results:
- Sevelamer treatment led to a 79.3% decrease in mitral valve calcification and improved aortic valve calcification scores.
- Significant slowing of renal function decline (p<0.001) was observed.
- Reduced serum concentrations of FGF-23 and CRP (p<0.0001) and urinary phosphorus excretion (p<0.0001) were noted.
Conclusions:
- One-year sevelamer treatment may impede cardiac valve calcification progression in CKD patients.
- Non-calcium-containing phosphate binders like sevelamer can slow renal function decline.
- Sevelamer effectively reduces FGF-23, CRP, and urinary phosphorus excretion, indicating broader benefits in CKD management.
Background:
No study has evaluated the efficacy of non-calcium-containing phosphate binders in slowing progression of cardiac valve calcification or deterioration of kidney function in patients with chronic kidney disease not on dialysis. This study addressed these issues.
Methods:
Outpatients (n = 170) with stage 3-4 chronic kidney disease and either mitral or aortic valve calcification were evaluated in this single-center, single-arm, prospective observational study. Patients received sevelamer hydrochloride (1,600 mg/day) for 1 year. Cardiac valve calcification progression was assessed by echocardiography, and decline of renal function by estimated glomerular filtration rate. Parathyroid hormone, FGF-23 and C-reactive protein (CRP) serum concentration and urinary phosphorus excretion were assayed.
Results:
At the end of treatment with sevelamer (12th month), mitral valve calcification had decreased by 79.3% from baseline. At baseline, 69 patients had grade 1, 97 patients grade 2 and 4 patients grade 3 calcification scores; at the end of the study, 60 patients showed grade 1, and no mitral valve calcification was registered in the remaining patients. An aortic valve score of 1 was found in 32%, score of 2 in 58%, score of 3 in 9% and score of 4 in 1% of patients at baseline; at the end of the study, a score of 1 was found in 95% and a score of 2 in 5% of patients. Significant slowing down of renal function decline (p<0.001), reduction of FGF-23 and CRP concentration (p<0.0001) and phosphorus excretion (p<0.0001) were observed.
Conclusions:
One-year treatment with a non-calcium-containing phosphate binder may hamper the progression of cardiac valve calcification and slow the decline of renal function, as well as reduce serum concentration of FGF-23 and CRP and urinary phosphorus excretion.
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