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Mortality in kidney disease patients treated with phosphate binders: a randomized study
Biagio Di Iorio1, Antonio Bellasi, Domenico Russo
1Department of Nephrology, Ospedale A. Landolfi di Solofra, Avellino, Italy. diiorio@gmail.com
Insights
Sevelamer use in chronic kidney disease patients reduced all-cause mortality and the combined endpoint of death or dialysis initiation. Further research is needed to confirm these findings on phosphate binder efficacy.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Pharmacology
Background:
- Dietary phosphorus overload and calcium intake from binders contribute to coronary artery calcification (CAC) and mortality in dialysis patients.
- CAC is prevalent even in early stages of non-dialysis-dependent chronic kidney disease (CKD).
- The impact of phosphate binders on mortality in non-dialysis-dependent CKD remains understudied.
Purpose of the Study:
- To evaluate the effect of different phosphate binders on all-cause mortality in non-dialysis-dependent CKD patients.
- To assess the impact on dialysis inception and a composite endpoint of mortality and dialysis initiation.
Main Methods:
- A randomized, multicenter, nonblinded pilot study involving 212 patients with stage 3-4 CKD.
- Patients were randomized to sevelamer (n=107) or calcium carbonate (n=105).
- Outcomes including all-cause mortality, dialysis inception, and CAC scores were monitored for up to 36 months.
Main Results:
- Sevelamer use was associated with lower all-cause mortality.
- The composite endpoint of death or dialysis inception was also lower in the sevelamer group.
- A trend towards lower dialysis inception was observed, though not statistically significant.
Conclusions:
- Sevelamer demonstrated benefits regarding all-cause mortality and the composite endpoint in non-dialysis-dependent CKD patients.
- No significant advantage was found for dialysis inception alone.
- Larger studies are required to validate these promising results.
Background And Objectives:
Dietary phosphorous overload and excessive calcium intake from calcium-containing phosphate binders promote coronary artery calcification (CAC) that may contribute to high mortality of dialysis patients. CAC has been found in patients in early stages of nondialysis-dependent CKD. In this population, no study has evaluated the potential role of phosphorus binders on mortality. This study aimed to evaluate all-cause mortality as the primary end point in nondialysis-dependent CKD patients randomized to different phosphate binders; secondary end points were dialysis inception and the composite end point of all-cause mortality and dialysis inception.
Design, Setting, Participants, & Measurements:
This is a randomized, multicenter, nonblinded pilot study. Consecutive outpatients (n=212; stage 3-4 CKD) were randomized to either sevelamer (n=107) or calcium carbonate (n=105). Phosphorus concentration was maintained between 2.7 and 4.6 mg/dl for patients with stage 3-4 CKD and between 3.5 and 5.5 mg/dl for patients with stage 5 CKD. The CAC score was assessed by computed tomography at study entry and after 6, 12, 18, and 24 months. All-cause mortality, dialysis inception, and the composite end point were recorded for up to 36 months.
Results:
In patients randomized to sevelamer, all-cause mortality and the composite end point were lower; a nonsignificant trend was noted for dialysis inception.
Conclusions:
Sevelamer provided benefits in all-cause mortality and in the composite end point of death or dialysis inception but not advantages in dialysis inception. Larger studies are needed to confirm these results.
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