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Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury

PURPOSE: To investigate the risk of acute kidney injury (AKI) in subjects initiating statin therapy for primary prevention of cardiovascular disease (CVD). METHODS: A nationwide cohort study using French hospital discharge and claims databases was performed, studying subjects from the general popula...

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Autores principales: Coste, Joël, Karras, Alexandre, Rudnichi, Annie, Dray‐Spira, Rosemary, Pouchot, Jacques, Giral, Philippe, Zureik, Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916201/
https://www.ncbi.nlm.nih.gov/pubmed/31517431
http://dx.doi.org/10.1002/pds.4898
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author Coste, Joël
Karras, Alexandre
Rudnichi, Annie
Dray‐Spira, Rosemary
Pouchot, Jacques
Giral, Philippe
Zureik, Mahmoud
author_facet Coste, Joël
Karras, Alexandre
Rudnichi, Annie
Dray‐Spira, Rosemary
Pouchot, Jacques
Giral, Philippe
Zureik, Mahmoud
author_sort Coste, Joël
collection PubMed
description PURPOSE: To investigate the risk of acute kidney injury (AKI) in subjects initiating statin therapy for primary prevention of cardiovascular disease (CVD). METHODS: A nationwide cohort study using French hospital discharge and claims databases was performed, studying subjects from the general population aged 40 to 75 years in 2009, with no history of CVD and no lipid‐lowering drugs during the preceding 3‐year period, followed for up to 7 years. Exposure to statins (type, dose, and time since first use) and to other drugs for CVD risk was assessed. The primary outcome was hospital admission for AKI. RESULTS: The cohort included 8 236 279 subjects, 818 432 of whom initiated a statin for primary prevention. During 598 487 785 person‐months exposed to statins, 700 events were observed, corresponding to an incidence of AKI of 4.59 per 10 000 person‐years (7.01 in men, 3.01 in women). AKI mainly occurred in the context of organ failure, sepsis, and genitourinary disease. A 19% increased rate of AKI (hazard ratio = 1.19, 95%CI: 1.08‐1.31) was observed in men exposed to statins, whereas no increase in the overall risk of AKI was observed in women. However, exposure to high‐potency statins was associated with a 72% to 116% increased risk in both genders and a dose‐effect relationship observed for rosuvastatin and atorvastatin. No temporal pattern of occurrence nor interaction with drugs for CVD risk was observed. CONCLUSIONS: Although the overall risk of AKI appears moderately increased, more attention should be paid to renal function in subjects taking statins for primary prevention both in clinical practice and from a research viewpoint.
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spelling pubmed-69162012019-12-17 Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury Coste, Joël Karras, Alexandre Rudnichi, Annie Dray‐Spira, Rosemary Pouchot, Jacques Giral, Philippe Zureik, Mahmoud Pharmacoepidemiol Drug Saf Original Reports PURPOSE: To investigate the risk of acute kidney injury (AKI) in subjects initiating statin therapy for primary prevention of cardiovascular disease (CVD). METHODS: A nationwide cohort study using French hospital discharge and claims databases was performed, studying subjects from the general population aged 40 to 75 years in 2009, with no history of CVD and no lipid‐lowering drugs during the preceding 3‐year period, followed for up to 7 years. Exposure to statins (type, dose, and time since first use) and to other drugs for CVD risk was assessed. The primary outcome was hospital admission for AKI. RESULTS: The cohort included 8 236 279 subjects, 818 432 of whom initiated a statin for primary prevention. During 598 487 785 person‐months exposed to statins, 700 events were observed, corresponding to an incidence of AKI of 4.59 per 10 000 person‐years (7.01 in men, 3.01 in women). AKI mainly occurred in the context of organ failure, sepsis, and genitourinary disease. A 19% increased rate of AKI (hazard ratio = 1.19, 95%CI: 1.08‐1.31) was observed in men exposed to statins, whereas no increase in the overall risk of AKI was observed in women. However, exposure to high‐potency statins was associated with a 72% to 116% increased risk in both genders and a dose‐effect relationship observed for rosuvastatin and atorvastatin. No temporal pattern of occurrence nor interaction with drugs for CVD risk was observed. CONCLUSIONS: Although the overall risk of AKI appears moderately increased, more attention should be paid to renal function in subjects taking statins for primary prevention both in clinical practice and from a research viewpoint. John Wiley and Sons Inc. 2019-09-13 2019-12 /pmc/articles/PMC6916201/ /pubmed/31517431 http://dx.doi.org/10.1002/pds.4898 Text en © 2019 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd. 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 Reports
Coste, Joël
Karras, Alexandre
Rudnichi, Annie
Dray‐Spira, Rosemary
Pouchot, Jacques
Giral, Philippe
Zureik, Mahmoud
Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title_full Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title_fullStr Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title_full_unstemmed Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title_short Statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
title_sort statins for primary prevention of cardiovascular disease and the risk of acute kidney injury
topic Original Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916201/
https://www.ncbi.nlm.nih.gov/pubmed/31517431
http://dx.doi.org/10.1002/pds.4898
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