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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),...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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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. |
format | Online Article Text |
id | pubmed-6629947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
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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