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Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus

Patients with type 2 diabetes mellitus (T2DM) have a very high risk of cardiovascular related events, and reducing complications is an important evaluation criterion of efficacy and safety of hypoglycemic drugs. Previous studies have shown that the dipeptidyl peptidase-4 (DPP-4) inhibitors (DPP4i),...

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Autores principales: Zeng, De-kang, Xiao, Qian, Li, Fa-qi, Tang, Yu-zhi, Jia, Chao-li, Tang, Xue-wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629947/
https://www.ncbi.nlm.nih.gov/pubmed/31262972
http://dx.doi.org/10.1042/BSR20190980
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author Zeng, De-kang
Xiao, Qian
Li, Fa-qi
Tang, Yu-zhi
Jia, Chao-li
Tang, Xue-wen
author_facet Zeng, De-kang
Xiao, Qian
Li, Fa-qi
Tang, Yu-zhi
Jia, Chao-li
Tang, Xue-wen
author_sort Zeng, De-kang
collection PubMed
description Patients with type 2 diabetes mellitus (T2DM) have a very high risk of cardiovascular related events, and reducing complications is an important evaluation criterion of efficacy and safety of hypoglycemic drugs. Previous studies have shown that the dipeptidyl peptidase-4 (DPP-4) inhibitors (DPP4i), such as sitagliptin, might reduce the incidence of major cardiovascular events (MACEs). However, the safety and efficacy of sitagliptin remains controversial, especially the safety for cardiovascular related events. Here, a systematic review was conducted to assess the cardiovascular safety of sitagliptin in T2DM patients. The literature research dating up to October 2018 was performed in the electronic database. The clinical trials about sitagliptin for T2DM patients were included. Two reviewers independently screened literature according to the inclusion and exclusion criteria. The primary outcome was the MACE, and the secondary outcome was all-cause mortality. Finally, 32 clinical trials composed of 16082 T2DM patients were included in this meta-analysis. The results showed that: there was no significant difference between sitagliptin group and the control group on MACE (odds ratio (OR) = 0.85, 95% confidence intervals (CIs) = 0.63–1.15), myocardial infarction (MI) (OR = 0.66, 95% CI = 0.38–1.16), stroke (OR = 0.83, 95% CI = 0.44–1.54) and mortality (OR = 0.52, 95% CI = 0.26–1.07). These results demonstrated that sitagliptin did not increase the risk of cardiovascular events in patients with T2DM.
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spelling pubmed-66299472019-07-24 Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus Zeng, De-kang Xiao, Qian Li, Fa-qi Tang, Yu-zhi Jia, Chao-li Tang, Xue-wen Biosci Rep Research Articles Patients with type 2 diabetes mellitus (T2DM) have a very high risk of cardiovascular related events, and reducing complications is an important evaluation criterion of efficacy and safety of hypoglycemic drugs. Previous studies have shown that the dipeptidyl peptidase-4 (DPP-4) inhibitors (DPP4i), such as sitagliptin, might reduce the incidence of major cardiovascular events (MACEs). However, the safety and efficacy of sitagliptin remains controversial, especially the safety for cardiovascular related events. Here, a systematic review was conducted to assess the cardiovascular safety of sitagliptin in T2DM patients. The literature research dating up to October 2018 was performed in the electronic database. The clinical trials about sitagliptin for T2DM patients were included. Two reviewers independently screened literature according to the inclusion and exclusion criteria. The primary outcome was the MACE, and the secondary outcome was all-cause mortality. Finally, 32 clinical trials composed of 16082 T2DM patients were included in this meta-analysis. The results showed that: there was no significant difference between sitagliptin group and the control group on MACE (odds ratio (OR) = 0.85, 95% confidence intervals (CIs) = 0.63–1.15), myocardial infarction (MI) (OR = 0.66, 95% CI = 0.38–1.16), stroke (OR = 0.83, 95% CI = 0.44–1.54) and mortality (OR = 0.52, 95% CI = 0.26–1.07). These results demonstrated that sitagliptin did not increase the risk of cardiovascular events in patients with T2DM. Portland Press Ltd. 2019-07-16 /pmc/articles/PMC6629947/ /pubmed/31262972 http://dx.doi.org/10.1042/BSR20190980 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Zeng, De-kang
Xiao, Qian
Li, Fa-qi
Tang, Yu-zhi
Jia, Chao-li
Tang, Xue-wen
Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title_full Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title_fullStr Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title_full_unstemmed Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title_short Cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
title_sort cardiovascular risk of sitagliptin in treating patients with type 2 diabetes mellitus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629947/
https://www.ncbi.nlm.nih.gov/pubmed/31262972
http://dx.doi.org/10.1042/BSR20190980
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