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Risk of incident diabetes among patients treated with statins: population based study
Objective To examine the risk of new onset diabetes among patients treated with different HMG-CoA reductase inhibitors (statins). Design Population based cohort study with time to event analyses to estimate the relation between use of particular statins and incident diabetes. Hazard ratios were calc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662830/ https://www.ncbi.nlm.nih.gov/pubmed/23704171 http://dx.doi.org/10.1136/bmj.f2610 |
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author | Carter, Aleesa A Gomes, Tara Camacho, Ximena Juurlink, David N Shah, Baiju R Mamdani, Muhammad M |
author_facet | Carter, Aleesa A Gomes, Tara Camacho, Ximena Juurlink, David N Shah, Baiju R Mamdani, Muhammad M |
author_sort | Carter, Aleesa A |
collection | PubMed |
description | Objective To examine the risk of new onset diabetes among patients treated with different HMG-CoA reductase inhibitors (statins). Design Population based cohort study with time to event analyses to estimate the relation between use of particular statins and incident diabetes. Hazard ratios were calculated to determine the effect of dose and type of statin on the risk of incident diabetes. Setting Ontario, Canada. Participants All patients aged 66 or older without diabetes who started treatment with statins from 1 August 1997 to 31 March 2010. The analysis was restricted to new users who had not been prescribed a statin in at least the preceding year. Patients with established diabetes before the start of treatment were excluded. Interventions Treatment with statins. Main outcome measure Incident diabetes. Results Compared with pravastatin (the reference drug in all analyses), there was an increased risk of incident diabetes with atorvastatin (adjusted hazard ratio 1.22, 95% confidence interval 1.15 to 1.29), rosuvastatin (1.18, 1.10 to 1.26), and simvastatin (1.10, 1.04 to 1.17). There was no significantly increased risk among people who received fluvastatin (0.95, 0.81 to 1.11) or lovastatin (0.99, 0.86 to 1.14). The absolute risk for incident diabetes was about 31 and 34 events per 1000 person years for atorvastatin and rosuvastatin, respectively. There was a slightly lower absolute risk with simvastatin (26 outcomes per 1000 person years) compared with pravastatin (23 outcomes per 1000 person years). Our findings were consistent regardless of whether statins were used for primary or secondary prevention of cardiovascular disease. Although similar results were observed when statins were grouped by potency, the risk of incident diabetes associated with use of rosuvastatin became non-significant (adjusted hazard ratio 1.01, 0.94 to 1.09) when dose was taken into account. Conclusions Compared with pravastatin, treatment with higher potency statins, especially atorvastatin and simvastatin, might be associated with an increased risk of new onset diabetes. |
format | Online Article Text |
id | pubmed-3662830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36628302013-05-24 Risk of incident diabetes among patients treated with statins: population based study Carter, Aleesa A Gomes, Tara Camacho, Ximena Juurlink, David N Shah, Baiju R Mamdani, Muhammad M BMJ Research Objective To examine the risk of new onset diabetes among patients treated with different HMG-CoA reductase inhibitors (statins). Design Population based cohort study with time to event analyses to estimate the relation between use of particular statins and incident diabetes. Hazard ratios were calculated to determine the effect of dose and type of statin on the risk of incident diabetes. Setting Ontario, Canada. Participants All patients aged 66 or older without diabetes who started treatment with statins from 1 August 1997 to 31 March 2010. The analysis was restricted to new users who had not been prescribed a statin in at least the preceding year. Patients with established diabetes before the start of treatment were excluded. Interventions Treatment with statins. Main outcome measure Incident diabetes. Results Compared with pravastatin (the reference drug in all analyses), there was an increased risk of incident diabetes with atorvastatin (adjusted hazard ratio 1.22, 95% confidence interval 1.15 to 1.29), rosuvastatin (1.18, 1.10 to 1.26), and simvastatin (1.10, 1.04 to 1.17). There was no significantly increased risk among people who received fluvastatin (0.95, 0.81 to 1.11) or lovastatin (0.99, 0.86 to 1.14). The absolute risk for incident diabetes was about 31 and 34 events per 1000 person years for atorvastatin and rosuvastatin, respectively. There was a slightly lower absolute risk with simvastatin (26 outcomes per 1000 person years) compared with pravastatin (23 outcomes per 1000 person years). Our findings were consistent regardless of whether statins were used for primary or secondary prevention of cardiovascular disease. Although similar results were observed when statins were grouped by potency, the risk of incident diabetes associated with use of rosuvastatin became non-significant (adjusted hazard ratio 1.01, 0.94 to 1.09) when dose was taken into account. Conclusions Compared with pravastatin, treatment with higher potency statins, especially atorvastatin and simvastatin, might be associated with an increased risk of new onset diabetes. BMJ Publishing Group Ltd. 2013-05-23 /pmc/articles/PMC3662830/ /pubmed/23704171 http://dx.doi.org/10.1136/bmj.f2610 Text en © Carter et al 2013 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Research Carter, Aleesa A Gomes, Tara Camacho, Ximena Juurlink, David N Shah, Baiju R Mamdani, Muhammad M Risk of incident diabetes among patients treated with statins: population based study |
title | Risk of incident diabetes among patients treated with statins: population based study |
title_full | Risk of incident diabetes among patients treated with statins: population based study |
title_fullStr | Risk of incident diabetes among patients treated with statins: population based study |
title_full_unstemmed | Risk of incident diabetes among patients treated with statins: population based study |
title_short | Risk of incident diabetes among patients treated with statins: population based study |
title_sort | risk of incident diabetes among patients treated with statins: population based study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662830/ https://www.ncbi.nlm.nih.gov/pubmed/23704171 http://dx.doi.org/10.1136/bmj.f2610 |
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