Sevelamer Use and Mortality in People with Chronic Kidney Disease Stages 4 and 5 Not on Dialysis

Author:

Molina Pablo12ORCID,Molina Mariola D.3ORCID,Carrero Juan J.4,Escudero Verónica1,Torralba Javier5,Castro-Alonso Cristina1ORCID,Beltrán Sandra1,Vizcaíno Belén12,González-Moya Mercedes12,Kanter Julia1,Sancho-Calabuig Asunción12ORCID,Bover Jordi6ORCID,Górriz José L.27ORCID

Affiliation:

1. Department of Nephrology, Hospital Universitari Dr. Peset, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana, 46017 Valencia, Spain

2. Department of Medicine, Universitat de València, 46010 Valencia, Spain

3. Department of Mathematics, Universidad de Alicante, 03690 Sant Vicent del Raspeig, Spain

4. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, SE-171 77 Stockholm, Sweden

5. Department of Nephrology, Hospital General Universitario, 03010 Alicante, Spain

6. Nephrology Department, University Hospital Germans Trias i Pujol, 08916 Badalona, Spain

7. Department of Nephrology, Hospital Clínico Universitario, Fundación para la Investigación del Hospital Clínico de la Comunidad Valenciana, 46010 Valencia, Spain

Abstract

Rationale and objective: Data suggest that non-calcium-based binders, and specifically sevelamer, may lead to lower rates of death when compared with calcium-based binders in end-stage renal disease (ESRD) patients. However, the association between sevelamer use and mortality for those with non-dialysis-dependent chronic kidney disease (NDD-CKD) patients has been uncertain. Study design: Our research is presented in a prospective cohort study. Setting and participants: A total of 966 participants with NDD-CKD stages 4–5 were enrolled in the PECERA study from 12 centers in Spain. Exposure: The participants were treated with sevelamer. Outcome: This study yielded all-cause and cardiovascular mortality outcomes. Analytical approach: We conducted an association analysis between mortality and sevelamer use with time-dependent Cox proportional hazards models. Results: After a median follow-up of 29 months (IQR: 13–36 months), death occurred in 181 participants (19%), with cardiovascular (n = 95, 53%) being the leading cause of death. In a multivariable model, the adjusted hazard ratios (HRs) for patients under sevelamer treatment were 0.44 (95% CI, 0.22 to 0.88) and 0.37 (95% CI, 0.18 to 0.75) for all-cause and cardiovascular mortality, respectively, compared with those of untreated patients. Limitations: Some limitations include potential confusion via indication bias; causal statements about these associations cannot be made due to the observational nature of this study. Conclusions: In this prospective NDD-CKD cohort study, the administration of sevelamer was independently associated with lower all-cause and cardiovascular mortality, suggesting that non-calcium-based phosphate binders might be the first-line therapy for phosphate lowering in this population. Further interventional studies clarifying the risks and benefits of phosphate binders in NDD-CKD are warranted.

Funder

the Valencian Society of Nephrology, the Spanish Society of Nephrology, and the Tomás de Osma Renal Foundation

bbott, Hoffmann-La Roche and Boehringer Ingelheim

Publisher

MDPI AG

Subject

General Medicine

Reference54 articles.

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