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DC Field | Value | Language |
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dc.contributor.author | J. Kongwatcharapong | en_US |
dc.contributor.author | P. Dilokthornsakul | en_US |
dc.contributor.author | S. Nathisuwan | en_US |
dc.contributor.author | A. Phrommintikul | en_US |
dc.contributor.author | N. Chaiyakunapruk | en_US |
dc.date.accessioned | 2018-09-05T03:09:39Z | - |
dc.date.available | 2018-09-05T03:09:39Z | - |
dc.date.issued | 2016-05-15 | en_US |
dc.identifier.issn | 18741754 | en_US |
dc.identifier.issn | 01675273 | en_US |
dc.identifier.other | 2-s2.0-84962810190 | en_US |
dc.identifier.other | 10.1016/j.ijcard.2016.02.146 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84962810190&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/56148 | - |
dc.description.abstract | © 2016 Elsevier Ireland Ltd. All rights reserved. Background: Recent studies have suggested that dipeptidyl peptidase-4 inhibitors (DPP-4 inhibitors) may be associated with increased risk of heart failure (HF), but evidence was inconclusive. We aimed to determine the effects of DPP-4 inhibitors on risk of HF. Methods: An extensive search in PubMed, EMBASE, CINAHL, IPA, Cochrane, ClinicalTrial.gov and the manufacturers' websites for randomized controlled trials (RCT) of all DPP-4 inhibitors was performed up to June 2015. All RCTs comparing DPP-4 inhibitors to any comparators with minimum follow-up of 12 weeks were included. The primary outcome was the occurrence of HF. Results: A total of 54 studies with 74,737 participants were included for analysis. Overall, DPP-4 inhibitors were not associated with an increased risk of HF compared to comparators (relative risk (RR) 1.106; 95% CI 0.995-1.228; p = 0.062). When analyzed individually, saxagliptin was significantly associated with the increased risk of HF (RR 1.215; 95% CI, 1.028-1.437; p = 0.022), while others were not. Age ≥ 65 years, diabetes duration of ≥ 10 years and BMI ≥ 30 kg/m2were associated with an increased risk of HF among patients using saxagliptin. Conclusions: Our meta-analysis suggested a differential effect of each DPP-4 inhibitor on the risk of HF. Use of saxagliptin significantly increases the risk of HF by 21% especially among patients with high CV risk while no signals were detected with other agents. This information should be taken into consideration when prescribing DDP-4 inhibitors. | en_US |
dc.subject | Medicine | en_US |
dc.title | Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | International Journal of Cardiology | en_US |
article.volume | 211 | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | University of Colorado Health Sciences Center | en_US |
article.stream.affiliations | Naresuan University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Monash University Malaysia | en_US |
article.stream.affiliations | University of Queensland | en_US |
article.stream.affiliations | University of Wisconsin Madison | en_US |
Appears in Collections: | CMUL: Journal Articles |
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