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Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis
BACKGROUND: Recommendations have not yet been established for statin therapy in patients on maintenance dialysis. In this study, we aimed to evaluate the effects of statin therapy on all‐cause mortality in patients undergoing maintenance hemodialysis. METHODS AND RESULTS: This retrospective cohort s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335561/ https://www.ncbi.nlm.nih.gov/pubmed/32089045 http://dx.doi.org/10.1161/JAHA.119.014840 |
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author | Jung, Jaehun Bae, Gi Hwan Kang, Minsun Kim, Soo Wan Lee, Dae Ho |
author_facet | Jung, Jaehun Bae, Gi Hwan Kang, Minsun Kim, Soo Wan Lee, Dae Ho |
author_sort | Jung, Jaehun |
collection | PubMed |
description | BACKGROUND: Recommendations have not yet been established for statin therapy in patients on maintenance dialysis. In this study, we aimed to evaluate the effects of statin therapy on all‐cause mortality in patients undergoing maintenance hemodialysis. METHODS AND RESULTS: This retrospective cohort study analyzed data from adults, aged ≥30 years, who were on maintenance hemodialysis for end‐stage renal disease. Data on statin use, along with other clinical information between 2007 and 2017, were extracted from the Health Insurance Review and Assessment Service database in Korea. In total, 65 404 patients were included, and 41 549 (73.2%) patients had received statin therapy for a mean duration of 3.6±2.6 years. Compared with statin nonusers before and after the initiation of hemodialysis (entry), patients who initiated statin therapy after entry and patients who continued statins from the pre–end‐stage renal disease to post–end‐stage renal disease period had a lower risk of all‐cause mortality; the adjusted hazard ratios (95% CIs) were 0.48 (0.47–0.50; P<0.001) for post–end‐stage renal disease only statin users and 0.59 (0.57–0.60; P<0.001) for continuous statin users. However, those discontinuing statins before or at entry showed a higher risk of all‐cause mortality. Statin‐ezetimibe combinations were associated with better survival benefits than fixed patterns of statin therapy. These results were consistent across various subgroups, including elderly patients aged >75 years, and were maintained even after propensity score matching. CONCLUSIONS: Our results showed that in adult patients undergoing maintenance hemodialysis, statin therapy, preferably combined with ezetimibe, was associated with a lower risk of all‐cause mortality. |
format | Online Article Text |
id | pubmed-7335561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73355612020-07-08 Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis Jung, Jaehun Bae, Gi Hwan Kang, Minsun Kim, Soo Wan Lee, Dae Ho J Am Heart Assoc Original Research BACKGROUND: Recommendations have not yet been established for statin therapy in patients on maintenance dialysis. In this study, we aimed to evaluate the effects of statin therapy on all‐cause mortality in patients undergoing maintenance hemodialysis. METHODS AND RESULTS: This retrospective cohort study analyzed data from adults, aged ≥30 years, who were on maintenance hemodialysis for end‐stage renal disease. Data on statin use, along with other clinical information between 2007 and 2017, were extracted from the Health Insurance Review and Assessment Service database in Korea. In total, 65 404 patients were included, and 41 549 (73.2%) patients had received statin therapy for a mean duration of 3.6±2.6 years. Compared with statin nonusers before and after the initiation of hemodialysis (entry), patients who initiated statin therapy after entry and patients who continued statins from the pre–end‐stage renal disease to post–end‐stage renal disease period had a lower risk of all‐cause mortality; the adjusted hazard ratios (95% CIs) were 0.48 (0.47–0.50; P<0.001) for post–end‐stage renal disease only statin users and 0.59 (0.57–0.60; P<0.001) for continuous statin users. However, those discontinuing statins before or at entry showed a higher risk of all‐cause mortality. Statin‐ezetimibe combinations were associated with better survival benefits than fixed patterns of statin therapy. These results were consistent across various subgroups, including elderly patients aged >75 years, and were maintained even after propensity score matching. CONCLUSIONS: Our results showed that in adult patients undergoing maintenance hemodialysis, statin therapy, preferably combined with ezetimibe, was associated with a lower risk of all‐cause mortality. John Wiley and Sons Inc. 2020-02-22 /pmc/articles/PMC7335561/ /pubmed/32089045 http://dx.doi.org/10.1161/JAHA.119.014840 Text en © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Jung, Jaehun Bae, Gi Hwan Kang, Minsun Kim, Soo Wan Lee, Dae Ho Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title | Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title_full | Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title_fullStr | Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title_full_unstemmed | Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title_short | Statins and All‐Cause Mortality in Patients Undergoing Hemodialysis |
title_sort | statins and all‐cause mortality in patients undergoing hemodialysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335561/ https://www.ncbi.nlm.nih.gov/pubmed/32089045 http://dx.doi.org/10.1161/JAHA.119.014840 |
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