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Sitagliptin and heart failure hospitalization in patients with type 2 diabetes

This study evaluated the risk of heart failure hospitalization in a 1:1 matched pair sample of sitagliptin ever and never users derived from the Taiwan's National Health Insurance. A total of 85,859 ever users and 85,859 never users matched on 8 digits of propensity score were followed for the...

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Autor principal: Tseng, Chin-Hsiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308758/
https://www.ncbi.nlm.nih.gov/pubmed/27409676
http://dx.doi.org/10.18632/oncotarget.10507
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author Tseng, Chin-Hsiao
author_facet Tseng, Chin-Hsiao
author_sort Tseng, Chin-Hsiao
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description This study evaluated the risk of heart failure hospitalization in a 1:1 matched pair sample of sitagliptin ever and never users derived from the Taiwan's National Health Insurance. A total of 85,859 ever users and 85,859 never users matched on 8 digits of propensity score were followed for the first event of heart failure hospitalization until December 31, 2011. The treatment effect (forever versus never users, and for tertiles of cumulative duration of therapy) was estimated by Cox regression incorporated with the inverse probability of treatment weighting using propensity score. Additionally, adjusted hazard ratios for heart failure were estimated for the baseline characteristics in sitagliptin ever users. Results showed that the incidence of heart failure hospitalization was 1,020.16 and 832.54 per 100,000 person-years, respectively, for ever and never users, with an overall hazard ratio (95% confidence intervals) of 1.262 (1.167-1.364). While compared to never users, the respective hazard ratio for the first, second, and third tertile of cumulative duration < 3.7, 3.7-10.3 and >10.3 months was 2.721 (2.449-3.023), 1.472 (1.318-1.645) and 0.515 (0.447-0.594). Older age, longer diabetes duration, male sex, and use of insulin, sulfonylurea, calcium channel blockers, aspirin, ticlopidine, clopidogrel and dipyridamole were significantly associated with a higher risk in sitagliptin users, but dyslipidemia and use of metformin and statin were protective. In conclusion, sitagliptin increases the risk of heart failure hospitalization within one year of its use, but reduces the risk thereafter. Some factors predisposing to sitagliptin-related heart failure are worthy of attention in clinical practice.
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spelling pubmed-53087582017-03-09 Sitagliptin and heart failure hospitalization in patients with type 2 diabetes Tseng, Chin-Hsiao Oncotarget Clinical Research Paper This study evaluated the risk of heart failure hospitalization in a 1:1 matched pair sample of sitagliptin ever and never users derived from the Taiwan's National Health Insurance. A total of 85,859 ever users and 85,859 never users matched on 8 digits of propensity score were followed for the first event of heart failure hospitalization until December 31, 2011. The treatment effect (forever versus never users, and for tertiles of cumulative duration of therapy) was estimated by Cox regression incorporated with the inverse probability of treatment weighting using propensity score. Additionally, adjusted hazard ratios for heart failure were estimated for the baseline characteristics in sitagliptin ever users. Results showed that the incidence of heart failure hospitalization was 1,020.16 and 832.54 per 100,000 person-years, respectively, for ever and never users, with an overall hazard ratio (95% confidence intervals) of 1.262 (1.167-1.364). While compared to never users, the respective hazard ratio for the first, second, and third tertile of cumulative duration < 3.7, 3.7-10.3 and >10.3 months was 2.721 (2.449-3.023), 1.472 (1.318-1.645) and 0.515 (0.447-0.594). Older age, longer diabetes duration, male sex, and use of insulin, sulfonylurea, calcium channel blockers, aspirin, ticlopidine, clopidogrel and dipyridamole were significantly associated with a higher risk in sitagliptin users, but dyslipidemia and use of metformin and statin were protective. In conclusion, sitagliptin increases the risk of heart failure hospitalization within one year of its use, but reduces the risk thereafter. Some factors predisposing to sitagliptin-related heart failure are worthy of attention in clinical practice. Impact Journals LLC 2016-07-09 /pmc/articles/PMC5308758/ /pubmed/27409676 http://dx.doi.org/10.18632/oncotarget.10507 Text en Copyright: © 2016 Tseng http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Tseng, Chin-Hsiao
Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title_full Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title_fullStr Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title_full_unstemmed Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title_short Sitagliptin and heart failure hospitalization in patients with type 2 diabetes
title_sort sitagliptin and heart failure hospitalization in patients with type 2 diabetes
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308758/
https://www.ncbi.nlm.nih.gov/pubmed/27409676
http://dx.doi.org/10.18632/oncotarget.10507
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