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Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression

BACKGROUND: The relationship between proton-pump inhibitor (PPI) use and chronic kidney disease (CKD) progression remains controversial. Specifically, there is a lack of data evaluating renal outcomes in established CKD patients. The aim of our study is to determine the risk of progression to end-st...

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Autores principales: Cholin, Liza, Ashour, Tarek, Mehdi, Ali, Taliercio, Jonathan J., Daou, Remy, Arrigain, Susana, Schold, Jesse D., Thomas, George, Nally, Joseph, Nakhoul, Nazih L., Nakhoul, Georges N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281649/
https://www.ncbi.nlm.nih.gov/pubmed/34266395
http://dx.doi.org/10.1186/s12882-021-02449-0
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author Cholin, Liza
Ashour, Tarek
Mehdi, Ali
Taliercio, Jonathan J.
Daou, Remy
Arrigain, Susana
Schold, Jesse D.
Thomas, George
Nally, Joseph
Nakhoul, Nazih L.
Nakhoul, Georges N.
author_facet Cholin, Liza
Ashour, Tarek
Mehdi, Ali
Taliercio, Jonathan J.
Daou, Remy
Arrigain, Susana
Schold, Jesse D.
Thomas, George
Nally, Joseph
Nakhoul, Nazih L.
Nakhoul, Georges N.
author_sort Cholin, Liza
collection PubMed
description BACKGROUND: The relationship between proton-pump inhibitor (PPI) use and chronic kidney disease (CKD) progression remains controversial. Specifically, there is a lack of data evaluating renal outcomes in established CKD patients. The aim of our study is to determine the risk of progression to end-stage kidney disease (ESKD) or death amongst CKD patients on PPI, histamine-2 receptor blocker (H2B), or no anti-acid therapy. METHODS: Using our CKD registry, we evaluated the relationship between PPI and H2B use and outcomes amongst patients with CKD (eGFR < 60), with at least 2 PCP visits in the year prior. A Cox proportional hazards model was used to evaluate the relationship between medication groups and overall mortality, while competing risks regression models were used to determine the risk of ESKD with death as a competing risk. RESULTS: 25,455 patients met inclusion criteria and were stratified according to medication group: no antacid therapy (15,961), PPI use (8646), or H2B use (848). At 4 years, the cumulative incidence of ESKD with death as a competing risk was 2.0% (95% CI: 1.7, 2.4), 1.5% (0.8, 2.8), and 1.6%(1.4, 1.9) among PPI, H2B, and no medication respectively (P = 0.22). The cumulative incidence of death with ESKD as a competing risk was 17.6% (95% CI: 16.6, 18.6), 16.7% (13.7, 19.8), and 17.3% (16.6, 18.0) (P = 0.71). CONCLUSIONS: Use of PPI in a CKD population was not associated with increased mortality or progression to ESKD when compared to H2 blocker and to no acid suppressing therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02449-0.
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spelling pubmed-82816492021-07-16 Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression Cholin, Liza Ashour, Tarek Mehdi, Ali Taliercio, Jonathan J. Daou, Remy Arrigain, Susana Schold, Jesse D. Thomas, George Nally, Joseph Nakhoul, Nazih L. Nakhoul, Georges N. BMC Nephrol Research BACKGROUND: The relationship between proton-pump inhibitor (PPI) use and chronic kidney disease (CKD) progression remains controversial. Specifically, there is a lack of data evaluating renal outcomes in established CKD patients. The aim of our study is to determine the risk of progression to end-stage kidney disease (ESKD) or death amongst CKD patients on PPI, histamine-2 receptor blocker (H2B), or no anti-acid therapy. METHODS: Using our CKD registry, we evaluated the relationship between PPI and H2B use and outcomes amongst patients with CKD (eGFR < 60), with at least 2 PCP visits in the year prior. A Cox proportional hazards model was used to evaluate the relationship between medication groups and overall mortality, while competing risks regression models were used to determine the risk of ESKD with death as a competing risk. RESULTS: 25,455 patients met inclusion criteria and were stratified according to medication group: no antacid therapy (15,961), PPI use (8646), or H2B use (848). At 4 years, the cumulative incidence of ESKD with death as a competing risk was 2.0% (95% CI: 1.7, 2.4), 1.5% (0.8, 2.8), and 1.6%(1.4, 1.9) among PPI, H2B, and no medication respectively (P = 0.22). The cumulative incidence of death with ESKD as a competing risk was 17.6% (95% CI: 16.6, 18.6), 16.7% (13.7, 19.8), and 17.3% (16.6, 18.0) (P = 0.71). CONCLUSIONS: Use of PPI in a CKD population was not associated with increased mortality or progression to ESKD when compared to H2 blocker and to no acid suppressing therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02449-0. BioMed Central 2021-07-15 /pmc/articles/PMC8281649/ /pubmed/34266395 http://dx.doi.org/10.1186/s12882-021-02449-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cholin, Liza
Ashour, Tarek
Mehdi, Ali
Taliercio, Jonathan J.
Daou, Remy
Arrigain, Susana
Schold, Jesse D.
Thomas, George
Nally, Joseph
Nakhoul, Nazih L.
Nakhoul, Georges N.
Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title_full Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title_fullStr Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title_full_unstemmed Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title_short Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression
title_sort proton-pump inhibitor vs. h2-receptor blocker use and overall risk of ckd progression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281649/
https://www.ncbi.nlm.nih.gov/pubmed/34266395
http://dx.doi.org/10.1186/s12882-021-02449-0
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